Issuu

Resources for You, Your Patients, & Your Practice

2025 BUYERS GUIDE

POC-24-NAM-5696

Meet the Quadruple Aim in Diabetes Care with In-office HbA1c and uACR Better outcomes. Lower costs. Better patient experience. Better clinician experience.

Diabetes management solutions at the point-of-care

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Gain insights into your patient’s current status with real-time actionable results. DCA Vantage® Analyzer Rapid assessment of glycemic control and kidney health HbA1c • CLIA-waived Albumin-to-creatinine ratio (ACR) • CLIA Moderate Complexity CLINITEK Status® Connect System CLIA-waived analyzer for routine urinalysis, including kidney health • CLINITEK® Microalbumin 2 Strip (ACR)

Total U.S. Population with Diabetes

The Prevalence of Diabetes Among U.S. Adults is on the Rise1 Help your patients reverse the trend Customize your patient consultations to enhance physician-patient partnership toward improved outcomes.

54% Increase

54,913,000 43,271,000 35,644,000

11.1%

2015

15.3% 13.0%

2020

2030 Projected

siemens-healthineers.us/chronicdisease

1. Rowley, William R et al. “Diabetes 2030: Insights from Yesterday, Today, and Future Trends.” Population health management vol. 20,1 (2017): 6-12. doi:10.1089/pop.2015.0181.

PUBLISHED BY Medical Education Resources, LLC PUBLISHER Aaron R. Medaris amedaris@physiciansofficeresource.com

CEO Andrew C. Nimmo acnimmo@physiciansofficeresource.com

PRESIDENT John D. Pasquale jpasquale@pharmaconnect.com

Getting the most from this guide There are two simple ways to request

BUSINESS MANAGER Marci J. Hills mhills@physiciansofficeresource.com

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2025 BUYERS GUIDE | 3

2025 BUYERS GUIDE

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2025 Medical Conferences

Diagnostics & Device Company Directory

Health Agency Hotlines

Government Organizations

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39 —

65 —

State Medical Associations

Companies by Categories

Product Guide

MDescapes Year of Destinations

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Early Detection, Rapid Diagnosis, Better Outcomes 4603

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For those seeking premium performance and reliable results Contact LifeSign Today (800) 526-2125 or email us at sales@lifesignmed.com MADE IN THE USA

To learn more about our full line of Rapid Diagnostic tests vist our website at www.lifesignmed.com to learn more about our products

PROVEN EFFECTIVE IN PATH, the largest Ig study in CIDP*

Improves functional ability Featuring proline for Ig stability

Important Safety Information Privigen is indicated for the treatment of: • Primary humoral immunodeficiency (PI) • Chronic immune thrombocytopenic purpura (ITP) in patients age 15 years and older • Chronic inflammatory demyelinating polyneuropathy (CIDP) in adults – Limitation of use: maintenance therapy in CIDP has not been studied for periods longer than 6 months. Individualize duration of treatment beyond 6 months based on patient response. WARNING: THROMBOSIS, RENAL DYSFUNCTION AND ACUTE RENAL FAILURE • Thrombosis may occur with immune globulin products, including Privigen. Risk factors may include advanced age, prolonged immobilization, hypercoagulable conditions, history of venous or arterial thrombosis, use of estrogens, indwelling vascular catheters, hyperviscosity, and cardiovascular risk factors. • Renal dysfunction, acute renal failure, osmotic nephrosis, and death may occur with immune globulin intravenous (IGIV) products in predisposed patients. Renal dysfunction and acute renal failure occur more commonly in patients receiving IGIV products that contain sucrose. Privigen does not contain sucrose.

• For patients at risk of thrombosis, renal dysfunction or renal failure, administer Privigen at the minimum dose and infusion rate practicable. Ensure adequate hydration in patients before administration. Monitor for signs and symptoms of thrombosis and assess blood viscosity in patients at risk for hyperviscosity. See full prescribing information for complete boxed warning. Privigen is contraindicated in patients with history of anaphylactic or severe systemic reaction to human immune globulin, in patients with hyperprolinemia, and in IgA-deficient patients with antibodies to IgA and a history of hypersensitivity. In patients at risk of developing acute renal failure, monitor urine output and renal function, including blood urea nitrogen and serum creatinine. Hyperproteinemia, increased serum viscosity, or hyponatremia can occur with Privigen. Infrequently, aseptic meningitis syndrome (AMS) may occur—especially with high doses or rapid infusion. Hemolysis, either intravascular or due to enhanced red blood cell sequestration, may occur. Risk factors include non-O blood group and high doses. Closely monitor patients for hemolysis and hemolytic anemia. During and shortly following Privigen infusion, elevations of systolic and diastolic blood pressure (including cases of hypertensive urgency) have been observed. These elevations resolved or significantly improved within hours with oral

PI & ITP SINCE 2007 >1 MILLION PATIENT-YEARS OF THERAPY1

CIDP SINCE 2017 Proven efficacy: Overall response rates to Privigen were 61% and 73% in PRIMA and PATH,* respectively†

Demonstrated tolerability: In both studies*, 97% of adverse reactions were mild or moderate in intensity with 2 and 8 subjects experiencing serious adverse reactions in PRIMA and PATH, respectively‡

Rapid response: Almost all who responded† to Privigen did so after 1–2 maintenance treatments at Weeks 4 and 7*

Information for you and your patients: Clinical information, patient resources, and videos at ConnectRx.com

Reference: 1. Data on file. Available from CSL Behring as PVG-006. *In a prospective, open-label, single-arm, multicenter clinical study (Privigen Impact on Mobility and Autonomy [PRIMA]), 28 subjects with CIDP received a Privigen loading dose of 2 g/kg followed by Privigen maintenance doses of 1 g/kg every 3 weeks for up to 21 weeks with 3-week follow-up. In a second prospective, open-label Privigen prerandomization phase of a multicenter clinical study (Polyneuropathy and Treatment with Hizentra [PATH]), 207 IVIg-pretreated subjects with CIDP received a Privigen loading dose of 2 g/kg followed by up to 4 Privigen maintenance doses of 1 g/kg every 3 weeks for up to 13 weeks. †Overall response rate was defined as percentage of subjects who experienced at least a 1-point decrease in adjusted INCAT score. ‡Serious adverse reactions included hemolysis (2), exacerbation of CIDP (2), acute rash, diastolic increased blood pressure, hypersensitivity, pulmonary embolism, respiratory failure, and migraine. A total of 4 patients discontinued treatment due to serious adverse reactions.

Visit the Privigen page at ConnectRx.com for more information and to access support resources anti-hypertensive therapy or observation alone. Check patients for a history of hypertension and monitor blood pressure during this period. Consider relative risks and benefits before prescribing high-dose regimen for chronic ITP and CIDP in patients at increased risk of thrombosis, hemolysis, acute kidney injury or volume overload. Monitor patients for pulmonary adverse reactions (transfusion-related acute lung injury [TRALI]). Privigen is derived from human plasma. The risk of transmission of infectious agents, including viruses and, theoretically, the Creutzfeldt-Jakob disease (CJD) agent and its variant (vCJD), cannot be completely eliminated. In clinical studies of patients with PI, the most common adverse reactions to Privigen, observed in >5% of subjects, were headache, fatigue, nausea, chills, vomiting, back pain, pain, elevated body temperature, abdominal pain, diarrhea, cough, stomach discomfort, chest pain, joint swelling/effusion, influenza-like illness, pharyngolaryngeal pain, urticaria, and dizziness. Serious adverse reactions were hypersensitivity, chills, fatigue, dizziness, and increased body temperature.

In clinical studies of patients being treated for chronic ITP, the most common adverse reactions, seen in >5% of subjects, were laboratory findings consistent with hemolysis, headache, elevated body temperature, anemia, nausea, and vomiting. A serious adverse reaction was aseptic meningitis syndrome. In clinical studies of patients being treated for CIDP, the most common adverse reactions observed in >5% of subjects, were headache, asthenia, hypertension, nausea, pain in extremity, hemolysis, influenza-like illness, leukopenia, and rash. Serious adverse reactions were hemolysis, exacerbation of CIDP, acute rash, increased diastolic blood pressure, hypersensitivity, pulmonary embolism, respiratory failure, and migraine. Treatment with Privigen might interfere with a patient’s response to live virus vaccines and could lead to misinterpretation of serologic testing. In patients over 65, do not exceed recommended dose and infuse at the minimum rate practicable. Please see the following brief summary of prescribing information for Privigen, including boxed warning.

BRIEF SUMMARY OF PRESCRIBING INFORMATION These highlights do not include all the information needed to use PRIVIGEN safely and effectively. See full prescribing information for PRIVIGEN. PRIVIGEN® Immune Globulin Intravenous (Human), 10% Liquid Initial U.S. Approval: 2007 WARNING: THROMBOSIS, RENAL DYSFUNCTION AND ACUTE RENAL FAILURE See full prescribing information for complete boxed warning. • Thrombosis may occur with immune globulin products, including PRIVIGEN. Risk factors may include: advanced age, prolonged immobilization, hypercoagulable conditions, history of venous or arterial thrombosis, use of estrogens, indwelling vascular catheters, hyperviscosity, and cardiovascular risk factors. • Renal dysfunction, acute renal failure, osmotic nephrosis, and death may occur with immune globulin intravenous (IGIV) products in predisposed patients. Renal dysfunction and acute renal failure occur more commonly in patients receiving IGIV products containing sucrose. PRIVIGEN does not contain sucrose. • For patients at risk of thrombosis, renal dysfunction or failure, administer PRIVIGEN at the minimum dose and infusion rate practicable. Ensure adequate hydration in patients before administration. Monitor for signs and symptoms of thrombosis and assess blood viscosity in patients at risk for hyperviscosity. ----------------------------INDICATIONS AND USAGE--------------------------PRIVIGEN is an Immune Globulin Intravenous (Human), 10% Liquid indicated for the treatment of: • Primary humoral immunodeficiency (PI) • Chronic immune thrombocytopenic purpura (ITP) in patients age 15 years and older • Chronic inflammatory demyelinating polyneuropathy (CIDP) in adults Limitations of Use: PRIVIGEN maintenance therapy in CIDP has not been studied beyond 6 months. ----------------------------CONTRAINDICATIONS--------------------------------• History of anaphylactic or severe systemic reaction to human immune globulin • Hyperprolinemia (PRIVIGEN contains the stabilizer L-proline) • IgA-deficient patients with antibodies to IgA and a history of hypersensitivity ---------------------------WARNINGS AND PRECAUTIONS-------------------• IgA-deficient patients with antibodies to IgA are at greater risk of developing severe hypersensitivity and anaphylactic reactions. • Monitor renal function, including blood urea nitrogen and serum creatinine, and urine output in patients at risk of developing acute renal failure. • Hyperproteinemia, increased serum viscosity, and hyponatremia may occur. • Aseptic meningitis syndrome (AMS) may occur, especially with high doses or rapid infusion. • Hemolysis that is either intravascular or due to enhanced red blood cell sequestration may occur. Risk factors include high doses and non-O blood group. Closely monitor patients for hemolysis and hemolytic anemia. • Elevations of systolic and diastolic blood pressure (including cases of hypertensive urgency) have been observed during/shortly following PRIVIGEN infusion. These blood pressure

Privigen is manufactured by CSL Behring AG and distributed by CSL Behring LLC. Privigen® is a registered trademark of CSL Behring AG. ©2024 CSL Behring LLC. 1020 First Avenue, PO Box 61501, King of Prussia, PA 19406-0901 USA www.CSLBehring.com www.Privigen.com USA-PVG-0059-AUG24

elevations were resolved or significantly improved within hours with either observation alone or changes in oral anti-hypertensive therapy. Check patients for a history of hypertension and monitor blood pressure during and following PRIVIGEN infusion. • Monitor patients for pulmonary adverse reactions (transfusion-related acute lung injury [TRALI]). • Carefully consider the relative risks and benefits before prescribing the high dose regimen (for chronic ITP and CIDP) in patients at increased risk of thrombosis, hemolysis, acute kidney injury, or volume overload. • PRIVIGEN is made from human blood and may contain infectious agents, e.g., viruses, the variant Creutzfeldt Jakob disease [vCJD] agent and, theoretically, the Creutzfeldt-Jakob disease (CJD) agent. ------------------------------ADVERSE REACTIONS------------------------------• PI – The most common adverse reactions, observed in >5% of study subjects, were headache, fatigue, nausea, chills, vomiting, back pain, pain, elevated body temperature, abdominal pain, diarrhea, cough, stomach discomfort, chest pain, joint swelling/effusion, influenza-like illness, pharyngolaryngeal pain, urticaria, and dizziness. Serious adverse reactions were hypersensitivity, chills, fatigue, dizziness, and increased body temperature. • Chronic ITP – The most common adverse reactions, observed in >5% of study subjects, were laboratory findings consistent with hemolysis (hemoglobin and hematocrit decrease without blood loss in conjunction with positive direct antiglobulin test (DAT) and elevated blood lactate dehydrogenase (LDH) and/or indirect bilirubin), headache, elevated body temperature, anemia, nausea, and vomiting. A serious adverse reaction was aseptic meningitis. • CIDP – The most common adverse reactions observed in >5% of study subjects were headache, asthenia, hypertension, nausea, pain in extremity, hemolysis, influenza like illness, leukopenia, and rash. Serious adverse reactions were hemolysis, exacerbation of CIDP, acute rash, blood pressure diastolic increased, hypersensitivity, pulmonary embolism, respiratory failure, and migraine. To report SUSPECTED ADVERSE REACTIONS, contact CSL Behring Pharmacovigilance at 1-866-915-6958 or FDA at 1-800-FDA-1088 or www.fda. gov/medwatch. -------------------------------DRUG INTERACTIONS-----------------------------The passive transfer of antibodies may: • Lead to misinterpretation of the results of serological testing. • Interfere with the response to live virus vaccines. ----------------------USE IN SPECIFIC POPULATIONS------------------------• Geriatric: In patients over age 65 or in any patient at risk of developing renal insufficiency, do not exceed the recommended dose, and infuse PRIVIGEN at the minimum rate practicable. See 17 for PATIENT COUNSELING INFORMATION. Based on March 2022 revision

THEY ARE IN YOUR WAITING ROOM RIGHT NOW. Patients with Peripheral Artery Disease (PAD) who may be facing a heart attack, stroke, amputation, or even death within the next 5 years.

1 OUT OF 3 HAS PAD

Diabetics

Smokers

Over age 65

AND THEY PROBABLY DON’T KNOW IT. ARE YOU TESTING THEM?

Atherosclerosis

Healthy Artery

Diseased Artery

P E R I P H E R A L (PAD) is an often silent condition where narrowed arteries reduce blood flow to ARTERY DISEASE the legs, causing symptoms like leg pain, numbness, and slow-healing wounds. DON’T LET PAD SNEAK UP ON YOU OR THESE PATIENTS. 50% report no symptoms, while those that do attribute their pain to arthritis or “old age”.

INTRODUCING

THESE PATIENTS TRUST YOU TO FIND THEIR PAD before they have a heart attack, stroke, or even die. PAD also leads to significant disability and reduced quality of life.

: A USER-FRIENDLY SOLUTION FOR EARLY PAD TESTING.

EASY No Doppler or vascular anatomy knowledge necessary. Can be done in five minutes or less by any staff member. Non-invasive, patient-friendly test. ACCURATE Accuracy equal or better than Doppler ABI. Useful for diabetics with calcified arteries. REIMBURSABLE Great ROI: the typical internist has 800 Medicare patients, per ACP. Testing five patients per week can pay for the system in less than two months. CPT 93923 (ABI w/exercise), with a national average of $142/exam.

4608

For over 45 years, Newman Medical has been a leader in vascular innovation. The ABI-Q system continues that legacy with fast, accurate results you can trust. Scan for more info

newman-medical.com | 800-267-5549 | info@newman-medical.com

| 2025 |

MEDICAL CONFERENCES

JANUARY

FEBRUARY

American Association for Hand Surgery 2025 Annual Meeting January 14 – 18, 2025 Big Island, Hawaii 978-927-8330 www.handsurgery.org

Pri-Med South February 6 – 8, 2025 Ft. Lauderdale, FL 877-477-4633 www.pri-med.com

American Society for Reconstructive Microsurgery Annual Meeting 2025 January 17 – 21, 2025 Big Island, Hawaii 312-456-9579 www.microsurg.org CANS Annual Meeting 2025 California Association of Neurological Surgeons January 17 - 19, 2025 Aptos, CA 916-457-2267 www.cans1.org STS Annual Meeting Society of Thoracic Surgeons January 24 – 26, 2025 Los Angeles, CA 312-202-5800 www.sts.org

ORS 2025 Annual Meeting Orthopaedic Research Society February 7 – 11, 2025 Phoenix, AZ 847-823-5770 www.ors.org Biophysical Society Annual Meeting 2025 Biophysical Society February 15 – 19, 2025 Los Angeles, CA 240-290-5600 www.biophysics.org/ 2025meeting#/ SCCM Critical Care Congress Society of Critical Care Medicine February 23 – 25, 2025 Orlando, FL 847-827-6888 www.sccm.org

10 | PHYSICIANS OFFICE RESOURCE

2025 AAAAI Annual Meeting American Academy of Allergy Asthma & Immunology February 28 – March 3, 2025 San Diego, CA 414-272-6071 www.annualmeeting. aaaai.org

MARCH 2025 Annual HIMSS Conference & Exhibition Healthcare Information and Management Systems March 3 – 6, 2025 Las, Vegas 855-326-8342 www.himssconference. org AAD Annual Meeting 2025 American Academy of Dermatology March 7 – 11, 2025 Orlando, FL 866-503-7546 www.aad.org/meetings/ annual-meeting

AAOS Annual Meeting 2025 American Academy of Orthopaedic Surgeons March 10 – 14, 2025 San Diego, CA 847-823-7186 www.aaos.org SAGES 2025 Annual Meeting Society of American Gastrointestinal Endoscopic Surgeons March 12 – 15, 2025 Long Beach, CA 310-437-0544 www.sages2025.org SGO 2025 Annual Meeting on Women’s Cancer Society of Gynecologic Oncologists March 14 – 17, 2025 Seattle, WA 312-235-4060 www.sgo.org The Aesthetic Meeting 2025 The American Society for Aesthetic Plastic Surgery March 20 – 23, 2025 Austin, TX 800-364-2147 www.surgery.org

2025 MEDICAL CONFERENCES AMGA Annual Conference 2025 American Medical Group Association March 26, – 29, 2025 Grapvine, TX 703-838-0033 www.amga.org SSO 2025 Annual Cancer Symposium Society of Surgical Oncology March 27 – 29, 2025 Tampa, FL 847-427-1400 www.surgonc.org AAC 2025 Annual Scientific Session and Expo American College of Cardiology March 29 – 31, 2025 Chicago, IL 800-253-4636 https://accscientificsession.acc.org SIR 2025 Annual Scientific Meeting Society of Interventional Radiology March 29 – April 2, 2025 Nashville, TN 800-488-7284 www.SIRmeeting.org

APRIL AAPM Annual Meeting American Academy of Pain Medicine April 3 – 6, 2025 Austin, TX 847-375-4731 https://painconnect.org

ACP Internal Medicine Meeting 2025 American College of Physicians April 3 – 5, 2025 New Orleans, LA 800-523-1546 https://annualmeeting. acponline.org/

AANS Annual Scientific Meeting 2025 American Association of Neurological Surgeons April 25 – 28, 2025 Boston, MA 847-378-0500 www.aans.org

Scientific & Clinical Congress American Association of Clinical Endocrinologists May 15 – 17, 2025 Orlando, FL 904-353-7878 https://am.aace.com

AORN Global Surgical Conference & Expo 2025 Association of Perioperative Registered Nurses April 5 – 8, 2025 Boston, MA 800-755-2676 www.aorn.org

ARRS Annual Meeting 2025 American Roentgen Ray Society April 27 – May 1, 2025 San Diego, CA 866-940-2777 www.arrs.org

AANA Annual Congress 2025 Arthroscopy Association of North America May 8 – 10 2025 Washinton, DC 847-292-2262 www.aana.org

AAN Annual Meeting 2025 American Academy of Neurology April 5 – 9, 2025 San Deigo, CA 800-879-1960 www.aan.com

ASBS Annual Meeting 2025 American Society of Breast Surgeons April 30 – May 4, 2025 Las Vegas, NV 877-992-5470 www.breastsurgeons.org

MAY Pri-Med Southwest 2025 April 10 – 12, 2025 Houston, TX 877-774-6338 www.pri-med.com ASLMS 2025 Annual Conference American Society for Laser Medicine & Surgery April 24 – 26, 2025 Orlando, FL 877-258-6028 www.aslms.org AACR Annual Meeting 2025 American Association of Cancer Research April 25 – 30, 2025 Chicago, IL 866-423-3965 www.aacr.org

AATS Annual Meeting 2025 American Association for Thoracic Surgery May 2 – 5, 2025 Seattle, WA 978-927-8330 www.aats.org ACR Annual Meeting 2025 American College of Radiology May 3 – 7, 2025 Washington, DC 800-243-7419 www.acr.org/annual-meeting

ACOG 2025 Annual Clinical and Scientific Meeting American College of Obstetricians and Gynecologists May 16 – 18, 2025 Minneapolis, MN 800- 673-8444 www.acog.org ATS 2025 International Conference American Thoracic Society May 16 – 21, 2025 San Francisco, CA 212-315-8600 conference.thoracic.org ASNR Annual Meeting & The Foundation of the ASNR Symposium 2025 American Society of Neuroradiology May 17 – 21, 2025 Philadephia, PA 630-574-0220 www.asnr.org

Pri-Med West 2025 May 8 – 10, 2025 Anaheim, CA 877-774-6338 www.pri-med.com AACE 2025 Annual 2025 BUYERS GUIDE | 11

2025 MEDICAL CONFERENCES ACSM Annual Meeting American College of Sports Medicine May 27 – 30, 2025 Atlanta, GA 317-637-9200 www.acsm.org/annual-meeting/annual-home

JUNE

JULY ENDO Annual Meeting 2025 The Endocrine Society July 12 – 15, 2025 San Francisco, CA 888-363-6274 www.endocrine.org

AMA Annual Meeting of House of Delegates 2025 American Medical Association June 6 – 10, 2025 Chicago, Illinois 800-621-8335 www.ama-assn.org

AAPM Annual Meeting 2025 American Association of Physicists in Medicine July 27 – 30, 2025 Washington, DC 571-298-1300 www.aapm.org

APIC Annual Conference 2025 Association for Professional in Infection Control and Epidemiology June 16 – 18, 2025 Phoenix, AZ 202-789-1890 annual.apic.org

ADLM 2025 Annual Meeting & Clinical Lab Expo (Formerly AACC) Association for Diagnostics & Laboratory Medicine July 27 – 31, 2025 Chicago, IL 800-892-1400 www.aacc.org

BIO International Convention 2025 Biotechnology Industry Organization June 16 – 19, 2025 Boston, MA 202-962-6655 bio.org SNMMI 2025 Annual Meeting Society of Nuclear Medicine & Molecular Imaging June 21 – 24, 2025 New Orleans, LA 703-708-9000 www.snmmi.org

AUGUST PDA Annual Meeting Pacific Dermatologic Association August 22 – 24, 2025 San Diego, CA 888-388-8815 www.pacificderm.org

SEPTEMBER ACEP Annual Scientific Assembly 2025 American College of Emergency Physicians September 7 – 10, 2025 Salt Lake City, UT 800-798-1822 www.acep.org

12 | PHYSICIANS OFFICE RESOURCE

ASTRO Annual Meeting 2025 American Society for Therapeutic Radiology & Oncology September 28 – October 1, 2025 San Francisco, CA 703-502-1550 www.astro.org

OCTOBER FMX 2025 American Academy of Family Physicians October 5 – 9, 2025 Anaheim, CA 800-274-2237 www.aafp.org The ANESTHESIOLOGY 2025 Annual Meeting American Society of Anesthesiologists October 10 – 14, 2025 San Antonio, TX 847-825-5586 www.asahq.org CNS Annual Meeting 2025 Congress of Neurological Surgeons October 11 – 15, 2025 Houston, TX 847-240-2500 www.cns.org/annualmeeting ASHG 2025 American Society of Human Genetics October 14 – 18, 2025 Boston, MA 301-634-7300 www.ashg.org AAO Annual Meeting 2025 American Academy of Ophthalmology October 17 – 20, 2025 Orlando, FL 415-561-8500 www.aao.org

CHEST 2025 ACCP Annual Meeting American College of Chest Physicians October 19 – 22, 2025 Chicago, IL 800-343-2227 www.chestnet.org ISPE Annual Meeting 2025 International Society for Pharmaceutical Engineering October 26 – 29, 2025 Carlotte, NC 301-364-9201 www.ispe.org ASRM Scientific Congress and Expo 2025 American Society for Reproductive Medicine October 25 – 29, 2025 San Antonio, TX 205-978-5000 www.asrm.org

NOVEMBER ACAAI 2025 Annual Meeting American College of Allergy Asthma & Immunology November 6 – 10, 2025 Orlando, FL 847-427-1200 www.acaai.org NASS 2025 Annual Meeting North American Spine Society November 14 – 17, 2025 Denver, CO 630-230-3600 www.spine.org RSNA 2025 Scientific Assembly and Annual Meeting Radiological Society of North America November 30 – December 4, 2025 Chicago, IL 800-381-6660 www.rsna.org

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Physicians office Resource 2022 | Issue 8

Resources for You, Your Patients, & Your Practice

Point-of-care testing: A WINNING STRATEGY IN THE BATTLE AGAINST DIABETES PAGE 6

Luxurious Getaways and Special Offers Exclusively for Physicians PAGE 14

COULD YOUR PERSONAL FINANCES BENEFIT FROM EARLY INTERVENTION AND TREATMENT? | PAGE 36

DIAGNOSTIC + DEVICE COMPANY

DIRECTORY A

Abbott Hematology Division 4551 Great America Parkway Santa Clara CA 95054 408-982-4850 www.corelaboratory. abbott/int/en/offerings/ category/hematology Abbott Point of Care 400 College Road East Princeton, NJ 08540 800-827-7828 www.globalpointofcare. abbott/en/index.html Abbott Toxicology 829 Towne Center Dr. Pomona, CA 91767 888-831-6850 https://www.toxicology. abbott/us/en/index.html Aerolase 120 White Plains Rd Tarrytown, NY 10591 914-345-8300 www.aerolase.com

ALCOR Scientific Inc. 20 Thurber Blvd Smithfield, RI 02917 800-495-5270 www.alcorscientific.com Alfa Wassermann 4 Henderson Drive West Caldwell, NJ 07006 800-220-4488 www.alfawassermannus. com Allscripts 222 Merchandise Mart Plaza, Suite 2024 Chicago, IL 60654 800-334-8534 www.allscripts.com American Academy of Family Physicians 11400 Tomahawk Creek Parkway Leawood, KS 66211-2672 800-274-2237 www.aafp.org

American Screening Corporation 9742 St Vincent Ave. Ste 100 Shreveport, LA 71106 866-526-2873 www.americanscreeningcorp.com AMS Alliance 1790 N. Commerce Pkwy Weston, FL 33326 1 (954) 217-0040 www.kpmanalytics.com/ brands/ams-alliance Apyx Medical 5115 Ulmerton Road Clearwater, FL 33760 800-537-2790 www.apyxmedical.com Arkray 5198 W. 76th Street Edina, MN 55439 800-818-8877 www.arkrayusa.com

B BD 7 Loveton Circle Sparks, MD 21152 1-800-638-8663 www.bd.com

Beckman Coulter 5350 Lakeview Pkwy S Drive Indianapolis, IN 46268 800-526-3821 www.beckmancoulter. com Bone Index Finland Ltd. 3710 Rawlins St., Suite 1420 Dallas, TX 75219 469-805-5419 www.bindex.us bioMerieux 1201 S 4800 W Salt Lake City, UT 84104 www.biofiredx.com Bio-Rad Laboratories 1000 Alfred Nobel Drive Hercules, CA 94547 800-424-6723 www.bio-rad.com Bionix Development Corporation 1670 Indian Wood Circle Maumee, OH 43537 800-551-7096 www.bionix.com

2025 BUYERS GUIDE | 15

DIAGNOSTIC + DEVICE COMPANY DIRECTORY

The Brewer Company N88 W13901 Main Street, Suite 100 Menomonee Falls, WI 53051 888-273-9371 www.brewercompany. com Brymill Cryogenic Systems 105 Windermere Avenue Ellington, CT 06029 860-875-2460 www.brymill.com

Candela 3 Goodyear, Unit A Irvine, CA 92618 800-733-8550 www.candelamedical. com Carolina Liquid Chemistries 313 Gallimore Dairy Rd Greensboro, NC 27409 877-722-8910 www.carolinachemistries.com Cepheid 904 Caribbean Drive Sunnyvale, CA 94089 888-336-2743 www.cepheid.com Cerner Corporation 2800 Rockcreek Parkway North Kansas City, MO 64117 816-221-1024 www.cerner.com Clarity Diagnostics 1060 Holland Dr., Suite A Boca Raton, FL 33487 561-288-9028 www.claritydiagnostics. com

Clinical Diagnostics Solutions, Inc. 1800 NW 65th Avenue Plantation, FL 33313 954-791-1773 www.cdsolinc.com

Detecto 203 East Daugherty Street Webb City, MO 64870 800-641-2008 www.detecto.com

Co-Diagnostics, Inc. 3222 S Washington St. South Salt Lake, UT 84115 www.co-dx.com 801-438-1036 COLA 9881 Broken Land Parkway Suite 200 Columbia, MD 210463016 800-981-9883 www.cola.org

DRG International 841 Mountain Ave. Springfield, NJ 07081 973-564-7555 www.drg-international. com

Cooper Surgical 75 Corporate Dr. Trumbull, CT 06611 800-243-2463 www.coopersurgical. com CryoConcepts, LP 1100 Conroy Place Easton, PA 18040 855-355-2796 Cryoconcepts.com Cutera, Inc. 3240 Bayshore Boulevard Brisbane, CA 94005 415-657-5500 www.cutera.com

D The Daavlin Company 205 West Bement Street Bryan, OH 43506 419-636-6304 www.daavlin.com DermaMed Solutions, LLC 394 Parkmount Road P.O. Box 187 Lenni, PA 19052 610-358-4447 www.dermamedsolutions.com

16 | PHYSICIANS OFFICE RESOURCE

Drucker Diagnostics 168 Bradford Drive Port Matilda, PA 16870 877-231-3115 www.druckerdiagnostics.com

E ELITechGroup North America 370 West 1700 South Logan, UT 84321 800-354-8324 www.elitechgroup.com Erba Mannheim DSP Tower – South, 19th Floor Dubai Science Park Dubai, UAE www.erbamannheim. com Evoke Neuroscience 1115 Broadway, 12th FL. New York, NY 10010 917-261-6096 www.evokeneuroscience.com Exergen Corporation 400 Pleasant St. Watertown, MA 02472 1-800-422-3006 www.exergen.com

F FUJIFILM SonoSite, Inc. 21919 30th Drive SE Bothell, WA 980213904 877-657-8118 www.sonosite.com Futuremed 15700 Devonshire Street Granada Hills, CA 91344 800-222-6780 www.futuremed.com

G Greenway Health, LLC. 4301 W Boy Scout Blvd, Suite 800 Tampa, FL 33607 877.932.6301 www.greenwayhealth. com

H H&O Equipments Inc. 115 Fairchild St. Suite 370 Charleston, SC 29492 888-248-2838 www.ho-equipments. com Heine North America 10 Innovation Way Dover, NH 03820 603-742-7103 www.heine.com Helena Laboratories 1530 Lindbergh Drive Beaumont, TX 77707 800-231-5663 www.helena.com Hemocue 250 South Kraemer Blvd. Mailstop: B1.SW.11 Brea, CA 92821 800-881-1611 www.hemocue.us

Hemosure, Inc. 5358 Irwindale Ave., Unit A Irwindale, CA 91706 626-443-8255 www.hemosure.com Hill-Rom 130 E Randolph St. Suite 1000 Chicago, IL 60601 312-819-7200 www.hillrom.com Hologic, Inc. 250 Campus Drive Marlborough, MA 01752 508-263-2900 www.hologic.com Horiba Medical 9755 Research Dr. Irvine, CA 92618 800- 446-7422 www.horiba.com/usa/ medical

J Jant Pharmacal 16530 Ventura Blvd., Suite 512 Encino, CA 91436 800-676-5565 www.jantdx.com Jones Medical Instrument Company 200 Windsor Drive Oak Brook, IL 60523 800-323-7336 www.jonesmedical.com

K Korr Medical Technologies, Inc. 3487 W 2100 S, Building 300 Salt Lake City, UT 84119 877-895-3007 www.korr.com

Huntleigh Diagnostics 35 Portmanmoor Road Cardiff CF24 5HN Wales UK 800-323-1245 www.huntleigh-diagnostics.com

Interson Corporation 7150 Koll Center Parkway Pleasanton, CA 94566 925-462-4948 www.interson.com

Masimo 52 Discovery Irvine, CA 92618 949-297-7000 www.masimo.com

iSalus Healthcare 1 Virginia Avenue Suite 500 Indianapolis, IN 46204 888-280-6678 www.isalushealthcare. com

LifeSign 85 Orchard Road Skillman, NJ 08558 800-526-2125 www.lifesignmed.com

Medica Corporation 5 Oak Park Drive Bedford, MA 01730 800-777-5983 www.medicacorp.com Medical Device Depot 3230 Bethany Lane, Suite 8 Ellicott City, MD 21042 877-646-3300 www.medicaldevicedepot.com

Meridian Bioscience 3471 River Hills Drive Cincinnati, OH 45244 800-696-0739 www.meridianbioscience.com MIR - Medical International Research 5462 S. Westridge Drive New Berlin, WI 53151 262-565-6797 www.spirometry.com Medicus LIS 4555 NW 103rd Avenue Suite 105 Sunrise, FL 33351 888-643-8081 www.medicuslis.com Medpod 1460 Broadway New York, NY 10036 844-633-7631 www.medpodhealth. com Mercedes Scientific 12210 Rangeland Parkway Lakewood Ranch, FL 34211 800-331-2716 www.mercedesscientific. com Micro Direct 803 Webster St. Lewiston, ME 04240 800-588-3381 www.mdspiro.com Midmark 60 Vista Dr Versailles, OH 45380 937-526-3662 www.midmark.com Mindray USA Corp. 800 MacArthur Blvd. Mahwah, NJ 07430 800-288-2121 www.mindraynorthamerica.com

Morningside Medical Equipment 8970 Route 108 Suite C Columbia, MD 21045 800-675-1202 www.morningsidemedicalequipment.com My Inspection 4555 NW 103rd Avenue Suite 105 Sunrise, FL 33351 888-643-8081 www.myinspection.us

N NanoEnTek 240 Bear Hill Road, Suite 101 Waltham, MA 02451 781-472-2558 www.nanoentek.com Nasiff Associates, Inc. 841 County Route 37, Suite 1 Central Square, NY 13036 866-627-4332 www.nasiff.com ndd Medical Technologies 300 Brickstone Square Suite 604 Andover, MA 01810 978-470-0923 www.nddmed.com NeuroMetrix, Inc. 1000 Winter Street Waltham, MA 02451 Phone (888) 786 7287 www.neurometrix.com Newman Medical 5350 Vivian St., Unit C Arvada, CO 80002 800-267-5549 www.newman-medical. com

DIAGNOSTIC + DEVICE COMPANY DIRECTORY

Nihon Kohden 90 Icon Street Foothill Ranch, CA 92610 800-325-0283 www.nihonkohden.com Nonin Medical 13700 1st Avenue North Plymouth, MN 55441 800-356-8874 www.nonin.com Nova Biomedical 200 Prospect Street Waltham, MA 02545 781-894-0800 www.novabio.us

O Opti Medical Systems, Inc. 235 Hembree Park Drive Rosewell, GA 30076 800-490-6784 www.optimedical.com OraSure Technologies, Inc. 220 East First Street Bethlehem, PA 18015 800-869-3538 www.orasure.com Ortho Clinical Diagnostics 1001 Route 202 Raritan, NJ 08869 800-828-6316 www.orthoclinical.com Ototronix 5000 Township Parkway Saint Paul, MN 55110 855-696-2986 www.ototronix.com Owen Mumford, Inc. 1755 West Oak Commons Court Marietta, GA 30062 770- 977- 2226 www.owenmumford. com/us/

P pts Diagnostics 7736 Zionsville Road Indianapolis, IN 46268 877-870-5610 www.ptsdiagnostics. com Phreesia 434 Fayetteville St. #1400 Raleigh, NC 27601 888-654-7473 www.phreesia.com Physicians Office Resource A Division of Medical Education Resources, LLC 125 High Meadow Rd Newbury, NH 03255 603-417-7305 www.physiciansofficeresource.com Polymedco, Inc. 510 Furnace Dock Road Cortlandt Manor, NY 10567 800-431-2123 www.polymedco.com Premier Medical 1710 Romano Drive Plymouth Meeting, PA 19462 888-773-6872 www.premiermedicalco. com

Q Quest Diagnostics 500 Plaza Drive Secaucus, NJ 07094 973-520-2700 www.questdiagnostics. com QuidelOrtho 9975 Summers Ridge Rd. San Diego, CA 92121 858.552.1100 www.quidelortho.com

18 | PHYSICIANS OFFICE RESOURCE

R Radiometer America, Inc. 250 S. Kraemer Blvd. Brea, CA 92821 800-736-0600 www.radiometeramerica.com Randox Laboratories LTD. 55 Diamond Road, Crumlin, County Antrim United Kingdom, BT29 4QY 866-472-6369 www.randox.com Resmed Corporation 9001 Spectrum Center Blvd. San Diego, CA 92123 800-424-0737 www.resmed.com Roche Diagnostics Corp. 9115 Hague Road Indianapolis, IN 46250 800-428-5074 https://diagnostics. roche.com

Semler Scientific 2344 Walsh Ave Santa Clara, CA 95051 www.semlerscientific. com Sempermed USA 13900 49th St. North Clearwater, FL 33762 727-787-7250 www.sempermedusa. com SHL Telemedicine USA 90 Yigal Alon St. Tel Aviv 67891 Israel 972-3-5612212 www.shl-telemedicine. com Siemens Healthineers 40 Liberty Blvd Malvern, PA 19355 800-888-7436 www.usa.siemens.com SightDx 35 17th St Jericho, NY 11753 929-397-0567 www.sightdx.com/en-us

Schiller America, Inc. 10903 NW 33rd St. Doral, FL 33172 786-845-0620 www.schillerus.com

Smiths Medical 5200 Upper Metro Place, Suite 200 Dublin, OH 43017 800-258-5361 www.smiths-medical. com

SDI Diagnostics Ten Hampden Drive Easton, MA 02375 800-678-5782 www.sdidiagnostics.com

Stanbio Laboratory 1261 North Main Street Boerne, TX 78006 800-531-5535 www.ekfusa.com

Sekisui Diagnostics One Wall Street Burlington, MA 01803 781-652-7800 www.sekisuidiagnostics. com

Streck Labs 7002 S. 109th St. La Vista, NE 68128 800-228-6090 www.streck.com Sysmex America, Inc. 577 Aptakisic Rd. Lincolnshire, IL 60069 866-779-7639 www.sysmex.com/us

T Tanita Corporation of America, Inc. 2625 South Clearbrook Drive Arlington Heights, IL 60005 847-640-9241 www.tanita.com Thermo Fisher Scientific 168 Third Avenue Waltham, MA 02451 800-678-5599 www.thermofisher.com

Tosoh Bioscience 6000 Shoreline Court, Suite 101 South San Francisco, CA 94080 800-248-6764 www.tosohbiosciences. com

Vinyl Crafters 47 West Frederick Street Walkersville, MD 21793 800-286-8738 www.vcupholstery.com

Trinity Biotech 2823 Girts Rd. Jamestown, NY 14701 800-325-3424 www.trinitybiotech.com

Vitalograph 13310 W. 99th St. Lenexa, KS 66215 800-255-6626 www.vitalograph.com

Zanfel Laboratories, Inc. 1370 Northwest 114th St. #204 Clive, IA 50325 800-401-4002 www.zanfel.com Zoll 269 Mill Road Chelmsford, MA 01824 978-421-9655 www.zoll.com

Tuttnauer USA Co. 25 Power Drive Hauppauge, NY 11788 800-624-5836 www.tuttnauerusa.com

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HEALTH

AGENCIES Adoption National Adoption Center www.adopt.org (800) 862-3678 Aging National Aging Info and Referral Support Center www.nasuad.org (202) 898-2578 Alcohol Abuse Al-Anon Family Groups www.al-anon.alateen.org (757) 563-1600 Allergy/Asthma American Academy of Allergy, Asthma & Immunology www.aaaai.org (414) 272-6071 FARE/ Food Allergy Research & Education www.foodallergy.org (800) 929-4040 Alzheimer’s Disease Alzheimer’s Association www.alz.org (800) 272-3900 Anemia Aplastic Anemia & MDS International Foundation www.aamds.org (800) 747-2820

Sickle Cell Disease Association of America, Inc. www.sicklecelldisease. org (800) 421-8453 Arthritis Arthritis Foundation Info Hotline www.arthritis.org (844) 571-4357 Bladder Diseases Interstitial Cystitis Association www.ichelp.org (703) 442-2070 Blood Disorders National Hemophilia Foundation www.hemophilia.org (212) 328-3700 Bone Marrow National Bone Marrow Transplant Link www.nbmtlink.org (800) 546-5268 Bone Disease National Institute of Arthritis & Musculoskeletal & Skin Diseases www.niams.nih.gov (877) 226-4267

20 | PHYSICIANS OFFICE RESOURCE

Breast Disease National Breast & Cervical Cancer Early Detection Program www.cdc.gov/cancer/ nbccedp (800) 232-4636 Digestive Disorders/ Diseases Crohn’s & Colitis Foundation of America www.ccfa.org (800) 932-2423 Celiac Disease Foundation www.celiac.org (818) 716-1513 Eating Disorders National Eating Disorders Association www. nationaleatingdisorders. org (800) 931-2237 Eye Disease American Macular Degeneration Foundation www.macular.org (888) 622-8527 The Vision Council www.thevisioncouncil. org (866) 826-0290

Glaucoma Research Foundation www.glaucoma.org (415) 986-3162 Fibromyalgia National Fibromyalgia Association www.fmaware.org Gastrointestinal Diseases International Foundation for Functional Gastrointestinal Disorders www.iffgd.org (414) 964-1799 Growth Disorders Human Growth Foundation www.hgfound.org (800) 451-6434 Hearing Disorders International Hearing Society www.ihsinfo.org (734) 522-7200 Heart Disease American Heart Association www.heart.org (800) 242-8721 Hepatitis C Hepatitis C Association www.hepcassoc.org (908) 769-8479

HEALTH AGENCY HOTLINES

Hospital/Hospice Care Caring Connections www.caringinfo.org (703) 837-1500 Immunization National Immunization Hotline www.cdc.gov/vaccines (800) 232-4636 Impotence American Urological Association www.auanet.org (866) 746-4282 Insurance/Medicare/ Medicaid Medicare Issues Hotline www.medicare.gov (800) 633-4227 Kidney Disease National Kidney Foundation www.kidney.org (800) 622-9010 Lead EPA Lead Information Center www.epa.gov/lead (800) 424-5323 Liver Diseases American Liver Foundation www.liverfoundation.org (212) 668-1000 Lung Disease/Asthma/ Allergy American Lung Association www.lungusa.org (800) 586-4872 Mental Health Mental Health America www. mentalhealthamerica.net (800) 969-6642

Minority Health US Department of Health and Human Services Office of Minority Health www.minorityhealth.hhs. gov (800) 444-6472 Nervous System Disease American Parkinson Disease Association www.apdaparkinson.org (800) 223-2732 Multiple Sclerosis Foundation www.msfocus.org (888) 673-6287 National Stroke Association www.stroke.org (800) 242-8721 Organ Donation Living Bank www.livingbank.org (800) 528-2971 Pancreatic Disease Pancreatic Cancer Action Network www.pancan.org (877) 573-9971 Paralysis and Spinal Injury Christopher & Dana Reeve Foundation www.christopherreeve. org (800) 539-7309 Parkinson’s Disease Parkinson’s Disease Foundation www.parkinson.org (800) 473-4636 Pediatrics American Academy of Pediatrics www.aap.org (800) 433-9016

Poison Control American Association of Poison Control Centers www.aapcc.org (800) 222-1222

Surgery/Facial Plastic Surgery American Society of Plastic Surgeons www.plasticsurgery.org (847) 228-9900

Professionals American Medical Association www.ama-assn.org (800) 622-3211

Thyroid Disease American Thyroid Association www.thyroid.org (703) 998-8890

Rehabilitation National Rehabilitation Info. Ctr. www.naric.com (800) 346-2742

Veterans Veterans Special Issue Helpline Department of Veterans Affairs www.va.gov (844) 698-2311

Rheumatic Diseases Scleroderma Foundation www.scleroderma.org (800) 722-4673 Sexually Transmitted Diseases CDC Sexually Transmitted Diseases Info. www.cdc.gov/std/ (800) 232-4636

VA Suicide Prevention www.mentalhealth. va.gov (844) 698-2311 Vision Disorders American Council of the Blind www.acb.org (800) 424-8666

Skin Disease National Psoriasis Foundation www.psoriasis.org (800) 723-9166 Spinal Diseases National Scoliosis Foundation, Inc. www.scoliosis.org (800 )673-6922 Stroke National Stroke Association www.stroke.org (800) 242-8721 Sudden Infant Death Syndrome American SIDS Institute www.sids.org (239) 431-5425

2025 BUYERS GUIDE | 21

GOVERNMENT

ORGANIZATIONS Agency for Healthcare Research and Quality (301) 427-1104 www.ahrq.gov Center for Disease Control and Prevention (800) 232-4636 www.cdc.gov Centers for Medicare & Medicaid Services (800) 633-4227 www.cms.gov National Institute on Aging (800) 222-2225 www.nia.nih.gov National Institute on Alcohol Abuse and Alcoholism (NIAAA) (301) 443-2857 www.niaaa.nih.gov National Institute of Allergy and Infectious Diseases (866) 284-4107 www.niaid.nih.gov

National Institute of Arthritis and Musculoskeletal and Skin Disease (877) 226-4267 www.niams.nih.gov National Institute of Biomedical Imaging and Bioengineering (301) 496-8859 www.nibib.nih.gov National Institute of Child Health & Human Development (800) 370-2943 www.nichd.nih.gov National Institute of Dental and Craniofacial Research (866) 232-4528 www.nidcr.nih.gov National Institute of Diabetes and Digestive and Kidney Disease (800) 860-8747 www.niddk.nih.gov

22 | PHYSICIANS OFFICE RESOURCE

National Institute of Environmental Health Sciences (919) 541-3345 www.niehs.nih.gov

U.S. Department of Health & Human Services (877) 696-6775 www.hhs.gov

National Institute of Mental Health (866) 615-6464 www.nimh.nih.gov

U.S. National Library of Medicine (301) 496-6308 www.nlm.nih.gov

National Institute of Nursing Research (301) 496-0207 www.ninr.nih.gov National Institute on Drug Abuse (301) 443-1124 www.drugabuse.gov National Institutes of Health (301) 496-4000 www.nih.gov Occupational Safety & Health Administration (800) 321-6742 www.osha.gov

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STATE MEDICAL

ASSOCIATIONS Alabama www.alamedical.org (800) 239-6272

Illinois www.isms.org (800) 782-4767

Montana www.mmaoffice.org (406) 443-4000

Rhode Island www.rimed.org (401) 331-3207

Alaska www.asmadocs.org (907) 562-0304

Indiana www.ismanet.org (800) 257-4762

Nebraska www.nebmed.org (402) 474-4472

South Carolina www.scmedical.org (800) 327-1021

Arizona www.azmed.org (602) 347-6900

Iowa www.iowamedical.org (515) 223-1401

Nevada www.nvdoctors.org (775) 825-6788

South Dakota www.sdsma.org (605) 336-1965

Arkansas www.arkmed.org (501) 224-8967

Kansas www.kmsonline.org (800) 332-0156

New Hampshire www.nhms.org (603) 224-1909

Tennessee www.tnmed.org (615) 385-2100

California www.cmanet.org (800) 786-4262

Kentucky www.kyma.org (502) 426-6200

New Jersey www.msnj.org (609) 896-1766

Texas www.texmed.org (800) 880-1300

Colorado www.cms.org (720) 859-1001

Louisiana www.lsms.org (225) 763-8500

New Mexico www.nmms.org (505) 828-0237

Utah www.utahmed.org (801) 747-3500

Connecticut www.csms.org (203) 865-0587

Maine www.mainemed.com (207) 622-3374

New York www.mssny.org (516) 488-6100

Vermont www.vtmd.org (802) 223-7898

District of Columbia www.msdc.org (202) 466-1800

Maryland www.medchi.org (800) 492-1056

North Carolina www.ncmedsoc.org (919) 833-3836

Virginia www.msv.org (800) 746-6768

Delaware www.medsocdel.org (302) 366-1400

Massachusetts www.massmed.org (781) 893-4610

North Dakota www.ndmed.org (701) 223-9475

Washington www.wsma.org (206) 441-9762

Florida www.flmedical.org (850) 224-6627

Michigan www.msms.org (517) 337-1351

Ohio www.osma.org (800) 766-6762

West Virginia www.wvsma.org (304) 925-0342

Georgia www.mag.org (678) 303-9290

Minnesota www.mnmed.org (612) 378-1875

Oklahoma www.okmed.org (800) 522-9452

Hawaii www.hawaiimedicalassociation.org (808) 536-7702

Mississippi www.msmaonline.com (601) 853-6733

Oregon www.theoma.org (503) 619-8000

Wisconsin www.wisconsinmedicalsociety.org (608) 442-3800

Missouri www.msma.org (573) 636-5151

Pennsylvania www.pamedsoc.org (800) 228-7823

Idaho www.idmed.org (208) 344-7888

24 | PHYSICIANS OFFICE RESOURCE

Wyoming www.wyomed.org (307) 635-2424

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PRODUCT

CATEGORIES A1C

ALBUMIN

Abbott www.globalpointofcare. abbott

Siemens Healthcare Diagnostics www.siemens-healthineers.com

Hemocue America www.Hemocue.com Siemens Healthcare Diagnostics www.siemens-healthineers.com ABI Huntleigh Diagnostics www.huntleigh-diagnostics.com Newman Medical www.newman-medical. com

ALLERGY Jant Pharmacal www.accutest.net Jant Pharmacal www.medicaldevicedepot.com ASTHMA TESTING Micro Direct www.mdspiro.com Vitalograph www.vitalograph.com

ACNE Treatment

AUDIOMETRY

Theravant Corp www.theraclear.com

Ototronix www.ototronixdiagnostics.com

AESTHETICS Aerolase www.aerolase.com Alma Lasers www.almalasers.com Cutera www.cutera.com CryoProbe www.ho-equipments.com DermaMed www.dermamedsolutions. com

AUGMENTED MEDICINE Medpod www.medpodhealth.com BLOOD GAS Abbott Point of Care www.globalpointofcare. abbott

Welch Allyn www.welchallyn.com

Nihon Kohden www.nohonkohden.com

BONE HEALTH

Nonin Medical www.nonin.com

Bone Index Ltd. www.bindex.us BRAIN ASSESMENT Evoke Neuroscience www.evokeneuroscience. com Morningside Medical Equipment www.morningsidemedicalequipment.com CARDIO VASCULAR/ PULMONARY Abbott Rapid Diagnostics www.globalpointofcare. abbott

Schiller America, Inc. www.schillerus.com SDI Diagnostics Inc. www.sdidiagnostics.com Vitalograph www.vitalograph.com Welch Allyn www.welchallyn.com CENTRIFUGES Drucker Diagnostics www.druckerdiagnostics. com Chemistry Analyzers

Brilliant Medical www.brilliantmedical.com

Abbott Diagnostics www.corelaboratory. abbott

Futuremed America, Inc. www.futuremedamerica. com

Abbott Point of Care www.globalpointofcare. abbott

Medical Device Depot www.medicaldevicedepot.com

AMS Diagnostics www.amsdiagnostics.com

Micro Direct, Inc. www.mdspiro.com

Beckman Coulter www.beckmancoulter.com Arkray www.arkrayusa.com

Nova Biomedical www.novabiomedical.com

Midmark Diagnostics, Inc. www.midmark.com

BLOOD PRESSURE

MIR – Medical International Research www.spirometry.com

Carolina Liquid Chemistries, Inc. www.carolinachemistries. com

Nasiff Associates, Inc. www.nasiff.com

ELITech Group www.elitechgroup.com

ndd Medical Technologies www.nddmed.com

Horiba Medical www.horiba.com/us/en/ medical

Orasure Histofreezer www.histofreezer.com

Medical Device Depot www.medicaldevicedepot.com

Premier Medical Products www.premusa.com

Vitalograph www.vitalograph.com

26 | PHYSICIANS OFFICE RESOURCE

PRODUCT CATEGORIES

Jant Pharmacal www.accutest.net Medica Corporation www.medicacorp.com Randox Laboratories, USA www.randox.com Roche www.roche.com Sekisui www.sekisuidiagnostics. com

CONJUNCTIVITIS TESTS RPS Diagnostics www.rpsdetectors.com COVID-19 TESTS BD https://bdveritor.bd.com/ en-us bioMerieux www.biomerieux.com

Zoll www.zoll.com DOPPLERS Huntleigh Diagnostics www.huntleigh-diagnostics.com Medical Device Depot www.medicaldevicedepot.com

ECG Edan Diagnostics www.edandiagnostics. com GE Healthcare Technologies www.gehealthcare.com Medical Device Depot www.medicaldevicedepot.com

LumiraDx www.lumiradx.com

Newman Medical www.newman-medical. com

Vital Diagnostics www.vitaldiagnostics.com

LifeSign www.lifesignmed.com

Wallach Surgical Devices www.wallachsurgical.com

Mortara www.mortara.com

CHOLESTEROL & TRIGLYCERIDE TESTING

QuidelOrtho www.quidelortho.com

DRUGS OF ABUSE TESTS

Schiller America, Inc. www.schilleramerica.com

Abbott www.globalpointofcare. abbott

Sekisui Diagnostics www.sekisuidiagnostics. com

Alfa Wassermann, Inc www.alfawassermannus. com

CREATININE

Arkray www.arkrayusa.com

Siemens Healthcare Diagnostics www.siemens-healthineers.com

Beckman Coulter, Inc. www.beckman.com

CRYOSURGICAL DEVICES

Carolina Liquid Chemistries, Inc. www.carolinachemistries. com

CryoProbe www.ho-equipments.com

Carolina Liquid Chemistries www.carolinachemistries. com Horiba www.horiba.com/us/en/ medical Laboratory Consulting, LLC www.urinedrugscreenconsulting.com Randox Laboratories, Inc. www.randox.com

Midmark Diagnostics, Inc. www.midmark.com

Vitalograph www.vitalograph.com Welch Allyn www.welchallyn.com EDUCATION AAFP www.aafp.org COLA www.cola.org ELECTROLYTE

CryoConcepts, LP www.cryoconcepts.com

Sekisui www.sekisuidiagnostics. com

Abbott Point of Care www.globalpointofcare. abbott

DIABETES

EAR, NOSE & THROAT

Medica Corporation www.medicacorp.com

Abbott www.globalpointofcare. abbott

Bionix www.bionix.com

Medica Corporation www.medicacorp.com

PTS Diagnostics www.ptsdiagnostics.com

Semler Scientific www.semlerscientific.com

Randox Laboratories, Inc. www.randox.com

Siemens Healthcare Diagnostics www.siemens-healthineers.com

Horiba Medical www.horiba.com/us/en/ medical

COAGULATION Roche www.roche.com

DEFIBRILLATORS Medical Device Depot www.medicaldevicedepot.com

Brilliant Medical www.brilliantmedical.com HEINE Optotechnik www.heine.com Med-Electronics, Inc. www.med-electronics. com Welch Allyn, Inc. www.welchallyn.com

Opti Medical Systems, Inc. Roche www.roche.com ENDOSCOPY Pentax Medical www.pentaxmedical.com E-PRESCRIBING Amazing Charts www.amazingcharts.com

2025 BUYERS GUIDE | 27

PRODUCT CATEGORIES DrFirst www.drfirst.com ESR ALCOR Scientific www.alcorscientific.com EXAM ROOM FURNITURE Brewer Medical www.brewercompany.com Medical Device Depot www.medicaldevicedepot.com Midmark Corporation www.midmark.com Vinyl Crafters www.vcupholstery.com FECAL OCCULT BLOOD Beckman Coulter, Inc. www.beckmancoulter.com Clinical Genomics www.clinicalgenomics. com Hemosure, Inc. www.hemosure.com Jant Pharmacal www.accutest.net Sekisui www.sekisui.com FLU TESTING BD https://bdveritor.bd.com/ en-us bioMerieux www.BioFireDx.com LifeSign www.lifesignmed.com QuidelOrtho www.quidelortho.com Roche www.Roche.com Sekisui www.sekisuidiagnostics. com

GASTROINTESTINAL DISEASE TESTING bioMerieux www.biofiredx.com GLUCOSE TESTING Abbott Point of Care www.corelaboratory. abbott Abbott Rapid Diagnostics www.globalpointofcare. abbott Hemocue, Inc. www.hemocue.com Jant Pharmacal www.jantdx.com Nova Biomedical www.novabiomedical.com Roche go.roche.com/rochelancets H. PYLORI Sekisui www.sekisuidiagnostics. com

Horiba Medical www.horiba.com/us/en/ medical Jant Pharmacal www.accutest.net Sysmex America, Inc. www.sysmex.com/us HEMOGLOBIN ANALYZERS

Medicus LIS www.medicuslis.com Orchard Software www.orchardsoft.com LABORATORY SANATIZERS Clorox PDI

Abbott Rapid Diagnostics www.globalpointofcare. abbott

LAB SERVICES

EKF DIAGNOSTICS

COLA www.cola.org

Hemocue, Inc. www.hemocue.com Masimo Corporation www.masimo.com IMMUNOASSAY INSTRUMENTS Abbott Diagnostics www.corelaboratory. abbott

AAFP www.aafp.org

COLA Resources Inc. www.criedu.org Medicus Middleware www.medicusmiddleware. com My Inspection http://myinspection.us LANCETS

HCV – HIV TESTING

BD https://bdveritor.bd.com/ en-us

Roche go.roche.com/rochelancets

Orasure www.orasure.com

Beckman Coulter, Inc. www.beckmancoulter.com

LEAD TESTING

HEART DYSFUNCTION

NanoEnTek www.nanoentek.com

Semler Scientific www.semlerscientific.com HEMATOLOGY ANALYZERS Abbott www.corelaboratory.abbott/hematology

Sekisui Diagnostics www.sekisuidiagnostics. com INFECTIOUS DISEASE bioMerieux www.BioFireDx.com

Meridian Bioscience www.magellandx.com LIPID TESTING Abbott Rapid Diagnostics www.globalpointofcare. abbott METABOLIC TESTING

ALCOR Scientific www.alcorescientific.com

Roche www.roche.com

Korr Medical Technologies, Inc. www.korr.com

Beckman Coulter, Inc. www.beckmancoulter.com

Sekisui www.sekisui.com

MOBILE HEALTH TECHNOLOGY

Drucker Diagnostics, Inc. www.qbcdiagnostics.com

LABORATORY INFORMATION SYSTEMS

Medpod www.medpodhealth.com

Hemocue, Inc. www.hemocue.com

Alfa Wassermann, Inc

MONITORS

Jant Pharmacal www.accutest.net

Edan Diagnostics www.edandiagnostics.com

28 | PHYSICIANS OFFICE RESOURCE

PRODUCT CATEGORIES GE Healthcare Technologies www.gehealthcare.com Medical Device Depot www.medicaldevicedepot.com Midmark www.midmark.com Welch Allyn www.welchallyn.com NEUROLOGICAL TESTING Advanced Clinical Products www.advancedclinicalproducts.com Brilliant Medical www.brilliantmedical.com Evoke Neuroscience www.evokeneuroscience. com Morningside Medical Equipment www.morningsidemedicalequipment.com PAIN PRACTICE LAB Mercedes Medical www.mercedesmedical. com PERIPHERAL ARTERY DISEASE (PAD) Newman Medical www.newman-medical. com Semler Scientific www.semlerscientific.com PHOTOTHERAPY SOLUTIONS Daavlin Company www.daavlin.com PRACTICE MANAGEMENT Athena Health www.athenahealth.com ZirMed www.zirmed.com

PT/INR Roche www.Roche.com PULSE OXIMETERS Masimo Corporation www.masimo.com REAGENTS Abbott Diagnostics www.corelaboratory. abbott Beckman Coulter www.beckmancoulter.com Carolina Liquid Chemistries, Inc. www.carolinachemistries. com Randox Laboratories, USA www.randox.com Sekisui www.sekisuidiagnostics. com RESPIRATORY INFECTIONS BD https://bdveritor.bd.com/ en-us bioMerieux www.BioFireDx.com Cepheid www.cepheid.com LumiraDx www.lumiradx.com QuidelOrtho www.quidelortho.com Roche www.Roche.com Sekisui www.sekisuidiagnostics. com SLEEP DISORDERS ResMed www.resmed.com

SPIROMETRY Futuremed America, Inc. www.futuremedamerica. com

Medpod www.medpodhealth.com

Medical Device Depot www.medicaldevicedepot.com

Exergen Corporation www.exergen.com

Micro Direct, Inc. www.mdspiro.com

THERMOMETERS

TOXICOLOGY

Midmark Diagnostics, Inc. www.midmark.com

Abbott Clinical Laboratory Solutions www.diagnostics.abbott. com

MIR – Medical International Research www.spirometry.com

Mercedes Medical www.mercedesmedical. com

ndd Medical Technologies www.nddmed.com

Carolina Liquid Chemistries www.carolinachemistries. com

Vitalograph www.vitalograph.com

ULTRASOUND

Welch Allyn www.welchallyn.com

Interson www.interson.com

STREP TESTING

Samsung Medison www.samsungmedison. com

Alere, Inc. www.alere.com BD https://bdveritor.bd.com/ en-us Cepheid www.cepheid.com Beckman Coulter, Inc. www.beckmancoulter.com LifeSign, LLC www.lifesignmed.com QuidelOrtho www.quidelortho.com Roche www.roche.com Sekisui www.sekisuidiagnostics. com SYNDROMIC TESTING bioMerieux www.BioFireDx.com TELEHEALTH

URINALYSIS Abbott Rapid Diagnostics www.globalpointofcare. abbott Jant Pharmacal www.accutest.net LifeSign, LLC www.lifesignmed.com Roche www.roche.com Siemens Healthcare Diagnostics www.siemens-healthineers.com WOMEN’S HEALTH Sekisui Diagnostics www.sekisuidiagnostics. com WEIGHT MANAGEMENT Korr Medical Technologies, Inc. www.korr.com 2025 BUYERS GUIDE | 29

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BRIEF SUMMARY OF PRESCRIBING INFORMATION FOR BRUKINSA® (zanubrutinib) SEE PACKAGE INSERT FOR FULL PRESCRIBING INFORMATION 1 INDICATIONS AND USAGE 1.1 Mantle Cell Lymphoma BRUKINSA is indicated for the treatment of adult patients with mantle cell lymphoma (MCL) who have received at least one prior therapy. This indication is approved under accelerated approval based on overall response rate [see Clinical Studies (14.1)]. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial. 1.2 Waldenström’s Macroglobulinemia BRUKINSA is indicated for the treatment of adult patients with Waldenström’s macroglobulinemia (WM) [see Clinical Studies (14.2)]. 1.3 Marginal Zone Lymphoma BRUKINSA is indicated for the treatment of adult patients with relapsed or refractory marginal zone lymphoma (MZL) who have received at least one anti–CD20-based regimen. This indication is approved under accelerated approval based on overall response rate [see Clinical Studies (14.3)]. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial. 1.4 Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma BRUKINSA is indicated for the treatment of adult patients with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) [see Clinical Studies (14.4)]. 1.5 Follicular Lymphoma BRUKINSA is indicated for the treatment of adult patients with relapsed or refractory follicular lymphoma (FL), in combination with obinutuzumab, after two or more lines of systemic therapy. This indication is approved under accelerated approval based on response rate and durability of response [see Clinical Studies (14.5)]. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial. 4 CONTRAINDICATIONS None. 5 WARNINGS AND PRECAUTIONS 5.1 Hemorrhage Fatal and serious hemorrhage has occurred in patients with hematological malignancies treated with BRUKINSA. Grade 3 or higher hemorrhage including intracranial and gastrointestinal hemorrhage, hematuria, and hemothorax was reported in 3.8% of patients treated with BRUKINSA in clinical trials, with fatalities occurring in 0.2% of patients. Bleeding of any grade, excluding purpura and petechiae, occurred in 32% of patients.

6 ADVERSE REACTIONS The following clinically significant adverse reactions are discussed in more detail in other sections of the labeling: • Hemorrhage [see Warnings and Precautions (5.1)] • Infections [see Warnings and Precautions (5.2)] • Cytopenias [see Warnings and Precautions (5.3)] • Second Primary Malignancies [see Warnings and Precautions (5.4)] • Cardiac Arrhythmias [see Warnings and Precautions (5.5)] • Hepatotoxicity, including DILI [see Warnings and Precautions (5.6)] 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. The data in the WARNINGS AND PRECAUTIONS reflect exposure to BRUKINSA in nine monotherapy and 2 combination clinical trials, administered at 160 mg twice daily in 1608 patients and at 320 mg once daily in 121 patients. Among these 1729 patients, the median duration of exposure was 27.6 months, 78% of patients were exposed for at least 12 months, and 60% of patients were exposed for at least 24 months. In this pooled safety population, the most common adverse reactions (≥30%), including laboratory abnormalities, were neutrophil count decreased (51%), platelet count decreased (41%), upper respiratory tract infection (38%), hemorrhage (32%), and musculoskeletal pain (31%). Mantle Cell Lymphoma (MCL) The safety of BRUKINSA was evaluated in 118 patients with MCL who received at least one prior therapy in two single-arm clinical trials, BGB-3111-206 [NCT03206970] and BGB-3111-AU-003 [NCT02343120] [see Clinical Studies (14.1)]. The median age of patients who received BRUKINSA in studies BGB-3111-206 and BGB-3111-AU-003 was 62 years (range: 34 to 86), 75% were male, 75% were Asian, 21% were White, and 94% had an ECOG performance status of 0 to 1. Patients had a median of 2 prior lines of therapy (range: 1 to 4). The BGB-3111-206 trial required a platelet count ≥75 × 109/L and an absolute neutrophil count ≥1 × 109/L independent of growth factor support, hepatic enzymes ≤2.5 × upper limit of normal, total bilirubin ≤1.5 × ULN. The BGB-3111-AU-003 trial required a platelet count ≥50 × 109/L and an absolute neutrophil count ≥1 × 109/L independent of growth factor support, hepatic enzymes ≤3 × upper limit of normal, total bilirubin ≤1.5 × ULN. Both trials required a creatinine clearance (CLcr) ≥30 mL/min. Both trials excluded patients with prior allogeneic hematopoietic stem cell transplant, exposure to a BTK inhibitor, known infection with HIV, and serologic evidence of active hepatitis B or hepatitis C infection, and patients requiring strong CYP3A inhibitors or strong CYP3A inducers. Patients received BRUKINSA 160 mg twice daily or 320 mg once daily. Among patients receiving BRUKINSA, 79% were exposed for 6 months or longer, and 68% were exposed for greater than one year. Fatal adverse reactions within 30 days of the last dose of BRUKINSA occurred in 8 (7%) of 118 patients with MCL. Fatal cases included pneumonia in 2 patients and cerebral hemorrhage in one patient.

5.2 Infections Fatal and serious infections (including bacterial, viral, or fungal infections) and opportunistic infections have occurred in patients with hematological malignancies treated with BRUKINSA. Grade 3 or higher infections occurred in 26% of patients, most commonly pneumonia (7.9%), with fatal infections occurring in 3.2% of patients. Infections due to hepatitis B virus (HBV) reactivation have occurred.

Serious adverse reactions were reported in 36 patients (31%). The most frequent serious adverse reactions that occurred were pneumonia (11%) and hemorrhage (5%).

Consider prophylaxis for herpes simplex virus, pneumocystis jirovecii pneumonia, and other infections according to standard of care in patients who are at increased risk for infections. Monitor and evaluate patients for fever or other signs and symptoms of infection and treat appropriately.

Table 3 summarizes the adverse reactions in BGB-3111-206 and BGB-3111-AU-003.

5.3 Cytopenias Grade 3 or 4 cytopenias, including neutropenia (21%), thrombocytopenia (8%), and anemia (8%) based on laboratory measurements, developed in patients treated with BRUKINSA [see Adverse Reactions (6.1)]. Grade 4 neutropenia occurred in 10% of patients, and Grade 4 thrombocytopenia occurred in 2.5% of patients.

Of the 118 patients with MCL treated with BRUKINSA, 8 (7%) patients discontinued treatment due to adverse reactions in the trials. The most frequent adverse reaction leading to treatment discontinuation was pneumonia (3.4%). One (0.8%) patient experienced an adverse reaction leading to dose reduction (hepatitis B). Table 3: Adverse Reactions (≥10%) in Patients Receiving BRUKINSA in BGB-3111-206 and BGB-3111-AU-003 Trials Body System

Monitor complete blood counts regularly during treatment and interrupt treatment, reduce the dose, or discontinue treatment as warranted [see Dosage and Administration (2.4)]. Treat using growth factor or transfusions, as needed.

Infections and infestations

5.4 Second Primary Malignancies Second primary malignancies, including non-skin carcinoma, have occurred in 14% of patients treated with BRUKINSA. The most frequent second primary malignancy was non-melanoma skin cancers (8%), followed by other solid tumors in 7% of the patients (including melanoma in 1% of patients) and hematologic malignancies (0.7%). Advise patients to use sun protection and monitor patients for the development of second primary malignancies.

Skin and subcutaneous tissue disorders Gastrointestinal disorders

5.5 Cardiac Arrhythmias Serious cardiac arrhythmias have occurred in patients treated with BRUKINSA. Atrial fibrillation and atrial flutter were reported in 4.4% of patients treated with BRUKINSA, including Grade 3 or higher cases in 1.9% of patients. Patients with cardiac risk factors, hypertension, and acute infections may be at increased risk. Grade 3 or higher ventricular arrhythmias were reported in 0.3% of patients. Monitor for signs and symptoms of cardiac arrhythmias (e.g., palpitations, dizziness, syncope, dyspnea, chest discomfort), manage appropriately [see Dosage and Administration (2.4)], and consider the risks and benefits of continued BRUKINSA treatment. 5.6 Hepatotoxicity, Including Drug-Induced Liver Injury Hepatotoxicity, including severe, life-threatening, and potentially fatal cases of drug-induced liver injury (DILI), has occurred in patients treated with Bruton tyrosine kinase inhibitors, including BRUKINSA. Evaluate bilirubin and transaminases at baseline and throughout treatment with BRUKINSA. For patients who develop abnormal liver tests after BRUKINSA, monitor more frequently for liver test abnormalities and clinical signs and symptoms of hepatic toxicity. If DILI is suspected, withhold BRUKINSA. Upon confirmation of DILI, discontinue BRUKINSA.

Vascular disorders Musculoskeletal and connective tissue disorders Respiratory, thoracic, and mediastinal disorders

Percent of Patients (N=118) All Grades Grade 3 or % Higher %

Adverse Reaction Upper respiratory tract infectiona

Pneumoniab

10c

Urinary tract infection

0.8

Rashd

Bruisinge

Diarrhea

0.8

Constipation

Hypertension

3.4

3.4c

Musculoskeletal pain

3.4

Cough

Hemorrhagef g

Upper respiratory tract infection includes upper respiratory tract infection, upper respiratory tract infection viral. b Pneumonia includes pneumonia, pneumonia fungal, pneumonia cryptococcal, pneumonia streptococcal, atypical pneumonia, lung infection, lower respiratory tract infection, lower respiratory tract infection bacterial, lower respiratory tract infection viral. c Includes fatal adverse reaction. d Rash includes all related terms containing rash. e Bruising includes all related terms containing bruise, bruising, contusion, ecchymosis. f Hemorrhage includes all related terms containing hemorrhage, hematoma. g Musculoskeletal pain includes musculoskeletal pain, musculoskeletal discomfort, myalgia, back pain, arthralgia, arthritis. a

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Monitor for signs and symptoms of bleeding. Discontinue BRUKINSA if intracranial hemorrhage of any grade occurs. Consider the benefit-risk of withholding BRUKINSA for 3-7 days before and after surgery depending upon the type of surgery and the risk of bleeding.

Based on findings in animals, BRUKINSA can cause fetal harm when administered to a pregnant woman. Administration of zanubrutinib to pregnant rats during the period of organogenesis caused embryo-fetal toxicity, including malformations at exposures that were 5 times higher than those reported in patients at the recommended dose of 160 mg twice daily. Advise women to avoid becoming pregnant while taking BRUKINSA and for 1 week after the last dose. Advise men to avoid fathering a child during treatment and for 1 week after the last dose. If this drug is used during pregnancy, or if the patient becomes pregnant while taking this drug, the patient should be apprised of the potential hazard to a fetus [see Use in Specific Populations (8.1)].

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Bleeding has occurred in patients with and without concomitant antiplatelet or anticoagulation therapy. Coadministration of BRUKINSA with antiplatelet or anticoagulant medications may further increase the risk of hemorrhage.

5.7 Embryo-Fetal Toxicity

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Other clinically significant adverse reactions that occurred in <10% of patients with mantle cell lymphoma include major hemorrhage (defined as ≥ Grade 3 hemorrhage or CNS hemorrhage of any grade) (5%) and headache (4.2%).

Table 4: Selected Laboratory Abnormalitiesa (>20%) in Patients with MCL in Studies BGB-3111-206 and BGB-3111-AU-003 Percent of Patients (N=118)

Laboratory Parameter

All Grades (%)

Grade 3 or 4 (%)

Neutrophils decreased

Lymphocytosis

Hematologic abnormalities

Musculoskeletal pain includes back pain, arthralgia, pain in extremity, musculoskeletal pain, myalgia, bone pain, spinal pain, musculoskeletal chest pain, neck pain, arthritis, musculoskeletal discomfort. Hemorrhage includes epistaxis, hematuria, conjunctival hemorrhage, hematoma, rectal hemorrhage, periorbital hemorrhage, mouth hemorrhage, post procedural hemorrhage, hemoptysis, skin hemorrhage, hemorrhoidal hemorrhage, ear hemorrhage, eye hemorrhage, hemorrhagic diathesis, periorbital hematoma, subdural hemorrhage, wound hemorrhage, gastric hemorrhage, lower gastrointestinal hemorrhage, spontaneous hematoma, traumatic hematoma, traumatic intracranial hemorrhage, tumor hemorrhage, retinal hemorrhage, hematochezia, diarrhea hemorrhagic, hemorrhage, melena, post-procedural hematoma, subdural hematoma, anal hemorrhage, hemorrhagic disorder, pericardial hemorrhage, postmenopausal hemorrhage, stoma site hemorrhage, subarachnoid hemorrhage.

Clinically relevant adverse reactions in <10% of patients who received BRUKINSA included localized infection, atrial fibrillation or atrial flutter, and hematuria. Table 6 summarizes the laboratory abnormalities in ASPEN.

Platelets decreased

Hemoglobin decreased

Table 6: Select Laboratory Abnormalitiesa (≥20%) that Worsened from Baseline in Patients with WM Who Received BRUKINSA in Cohort 1

Blood uric acid increased

2.6

Laboratory Abnormality

ALT increased

0.9

Hematologic abnormalities

Bilirubin increased

0.9

Chemistry abnormalities

a b

Based on laboratory measurements. Asymptomatic lymphocytosis is a known effect of BTK inhibition.

Waldenström’s Macroglobulinemia (WM)

Among patients who received BRUKINSA, 93% were exposed for 6 months or longer, and 89% were exposed for greater than 1 year.

In Cohort 1, serious adverse reactions occurred in 44% of patients who received BRUKINSA. Serious adverse reactions in >2% of patients included influenza (3%), pneumonia (4%), neutropenia and neutrophil count decreased (3%), hemorrhage (4%), pyrexia (3%), and febrile neutropenia (3%). In Cohort 2, serious adverse reactions occurred in 39% of patients. Serious adverse reactions in >2 patients included pneumonia (14%). Permanent discontinuation of BRUKINSA due to an adverse reaction occurred in 2% of patients in Cohort 1 and included hemorrhage (1 patient), neutropenia and neutrophil count decreased (1 patient); in Cohort 2, permanent discontinuation of BRUKINSA due to an adverse reaction occurred in 7% of patients and included subdural hemorrhage (1 patient) and diarrhea (1 patient).

Dose reductions of BRUKINSA due to an adverse reaction occurred in 11% of patients in Cohort 1 and in 7% in Cohort 2. Adverse reactions which required dose reductions in >2% of patients included neutropenia in Cohort 1. Adverse reaction leading to dose reduction occurred in 2 patients in Cohort 2 (each with one event: diarrhea and pneumonia). Table 5 summarizes the adverse reactions in Cohort 1 in ASPEN.

Adverse Reaction

Infections and infestations

Upper respiratory tract infectiona Pneumoniab

Gastrointestinal disorders

General disorders

Skin and subcutaneous tissue disorders Musculoskeletal and connective tissue disorders Nervous system disorders Respiratory, thoracic, and mediastinal disorders Vascular disorders

a b

Hemoglobin decreased

Glucose increased

2.3

Creatinine increased

Calcium decreased

Potassium increased

Phosphate decreased

3.1

Urate increased

3.2

Bilirubin increased

Based on laboratory measurements. The denominator used to calculate the rate varied from 86 to 101 based on the number of patients with a baseline value and at least one post-treatment value.

Marginal Zone Lymphoma The safety of BRUKINSA was evaluated in 88 patients with previously treated MZL in two single-arm clinical studies, BGB-3111-214 and BGB-3111-AU-003 [see Clinical Studies (14.3)]. The trials required an absolute neutrophil count ≥1 × 109/L, platelet count ≥50 or ≥75 × 109/L and adequate hepatic function and excluded patients requiring a strong CYP3A inhibitor or inducer. Patients received BRUKINSA 160 mg twice daily (97%) or 320 mg once daily (3%). The median age in both studies combined was 70 years (range: 37 to 95), 52% were male, 64% were White, and 19% were Asian. Most patients (92%) had an ECOG performance status of 0 to 1. Eighty percent received BRUKINSA for 6 months or longer, and 67% received treatment for more than one year. Two fatal adverse reactions (2.3%) occurred within 30 days of the last dose of BRUKINSA, including myocardial infarction and a Covid-19–related death. Serious adverse reactions occurred in 40% of patients. The most frequent serious adverse reactions were pyrexia (8%) and pneumonia (7%). Adverse reactions lead to treatment discontinuation in 6% of patients, dose reduction in 2.3%, and dose interruption in 34%. The leading cause of dose modification was respiratory tract infections (13%).

Table 7: Adverse Reactions Occurring in ≥10% Patients with MZL Who Received BRUKINSA

BRUKINSA (N=101) Ibrutinib (N=98) All Grades Grade 3 All Grades Grade 3 (%) or 4 (%) (%) or 4 (%) 44

Body System

Adverse Reaction Upper respiratory tract infectiona

2 Infections and infestations

BRUKINSA (N=88) All Grades Grade 3 (%) or 4 (%) 26 3.4

Urinary tract infectionb

Pneumoniac,d

Diarrheae

3.4

Abdominal painf

2.3

Nausea

Vomiting

Bruisingg

Fatiguec

Rashh

Pyrexia

1.1

Edema peripheral

Urinary tract infection

Diarrhea

Nausea

Constipation

Gastrointestinal disorders

Skin and subcutaneous tissue disorders Musculoskeletal and connective tissue disorders

Musculoskeletal paini

2.3

Bruisingd

Vascular disorders

Hemorrhage

1.1

Rashe

General disorders

Fatiguek

2.3

Pruritus

Respiratory, thoracic, and mediastinal disorders

Coughl

Musculoskeletal painf Muscle spasms

Headache

Dizziness

Cough

Dyspnea

Hemorrhageg

Hypertension

Upper respiratory tract infection includes upper respiratory tract infection, laryngitis, nasopharyngitis, sinusitis, rhinitis, viral upper respiratory tract infection, pharyngitis, rhinovirus infection, upper respiratory tract congestion. Pneumonia includes lower respiratory tract infection, lung infiltration, pneumonia, pneumonia aspiration, pneumonia viral. c Fatigue includes asthenia, fatigue, lethargy. d Bruising includes all related terms containing bruise, contusion, or ecchymosis. e Rash includes all related terms rash, maculo-papular rash, erythema, rash erythematous, drug eruption, dermatitis allergic, dermatitis atopic, rash pruritic, dermatitis, photodermatoses, dermatitis acneiform, stasis dermatitis, vasculitic rash, eyelid rash, urticaria, skin toxicity. a

Table 7 summarizes selected adverse reactions in BGB-3111-214 and BGB-3111-AU-003.

Table 5: Adverse Reactions (≥10%) Occurring in Patients with WM Who Received BRUKINSA in Cohort 1 Body System

Neutrophils decreased Platelets decreased

Upper respiratory tract infection includes upper respiratory tract infection, nasopharyngitis, sinusitis, tonsillitis, rhinitis, viral upper respiratory tract infection. Urinary tract infection includes urinary tract infection, cystitis, Escherichia urinary tract infection, pyelonephritis, cystitis. c Pneumonia includes COVID-19 pneumonia, pneumonia, bronchopulmonary aspergillosis, lower respiratory tract infection, organizing pneumonia. d Includes 2 fatalities from COVID-19 pneumonia. e Diarrhea includes diarrhea and diarrhea hemorrhagic. f Abdominal pain includes abdominal pain, abdominal pain upper, abdominal discomfort. g Bruising includes contusion, ecchymosis, increased tendency to bruise, post procedural contusion. h Rash includes rash, rash maculo-papular, rash pruritic, dermatitis, dermatitis allergic, dermatitis atopic, dermatitis contact, drug reaction with eosinophilia and systemic symptoms, erythema, photosensitivity reaction, rash erythematous, rash papular, seborrheic dermatitis. i Musculoskeletal pain includes back pain, arthralgia, musculoskeletal pain, myalgia, pain in extremity, musculoskeletal chest pain, bone pain, musculoskeletal discomfort, neck pain. j Hemorrhage includes epistaxis, hematuria, hemorrhoidal hemorrhage, hematoma, hemoptysis, conjunctival hemorrhage, diarrhea hemorrhagic, hemorrhage urinary tract, mouth hemorrhage, pulmonary hematoma, subcutaneous hematoma, gingival bleeding, melena, upper gastrointestinal hemorrhage. k Fatigue includes fatigue, lethargy, asthenia. l Cough includes cough and productive cough. a

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Dosage interruptions of BRUKINSA due to an adverse reaction occurred in 32% of patients in Cohort 1 and in 29% in Cohort 2. Adverse reactions which required dosage interruption in >2% of patients included neutropenia, vomiting, hemorrhage, thrombocytopenia, and pneumonia in Cohort 1. Adverse reactions leading to dosage interruption in >2 patients in Cohort 2 included pneumonia and pyrexia.

Ibrutinibb

Chemistry abnormalities

The safety of BRUKINSA was investigated in two cohorts of Study BGB-3111-302 (ASPEN). Cohort 1 included 199 patients with MYD88 mutation (MYD88 MUT ) WM, randomized to and treated with either BRUKINSA (101 patients) or ibrutinib (98 patients). The trial also included a non-randomized arm, Cohort 2, with 26 wild type MYD88 (MYD88 WT ) WM patients and 2 patients with unknown MYD88 status [see Clinical Studies (14.2)].

In Cohort 1 of the ASPEN study safety population (N=101), the median age of patients who received BRUKINSA was 70 years (45-87 years old); 67% were male, 86% were White, 4% were Asian, and 10% were not reported (unknown race). In Cohort 2 of the ASPEN study safety population (N=28), the median age of patients who received BRUKINSA was 72 (39-87 years old); 50% were male, 96% were White, and 4% were not reported (unknown race).

BRUKINSAb

All Grades (%) Grade 3 or 4 (%) All Grades (%) Grade 3 or 4 (%)

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Clinically relevant adverse reactions in <10% of patients who received BRUKINSA included peripheral neuropathy, second primary malignancies, dizziness, edema, headache, petechiae, purpura, and atrial fibrillation or flutter.

Table 9: Adverse Reactions in ≥10% Patients with Previously Untreated CLL/SLL without 17p Deletion in SEQUOIA (Continued) CLL/SLL without 17p deletion

Table 8 summarizes select laboratory abnormalities. Table 8: Select Laboratory Abnormalities (≥20%) that Worsened from Baseline in Patients with MZL

System Organ Class Preferred Term

BRUKINSA

Laboratory Abnormalitya

BR (N=227)

All Grades (%)

Grade 3 or 4 (%)

All Grades (%)

Grade 3 or 4 (%)

13*

1.3

0.4

All Grades (%)

Grade 3 or 4 (%)

Neutrophils decreased

Platelets decreased

Headachee

Lymphocytes decreased

Dizzinessj

0.8

Hemoglobin decreased

Glucose increased

4.6

Creatinine increased

1.1

Phosphate decreased

2.3

Calcium decreased

ALT increased

1.1

Neoplasms

Hematologic abnormalities

Second primary malignancyi Nervous system disorders

Chemistry abnormalities

BRUKINSA (N=240)

The denominator used to calculate the rate varied from 87 to 88 based on the number of patients with a baseline value and at least one post-treatment value.

Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma The safety data described below reflect exposure to BRUKINSA (160 mg twice daily) in 675 patients with CLL from two randomized controlled clinical trials [see Clinical Studies (14.4)]. The trials required patients to be unsuitable for fludarabine, cyclophosphamide, and rituximab (FCR) therapy defined as age ≥65 years, or age 18 to <65 years with either a total Cumulative Illness Rating Scale (CIRS) >6, CLcr 30 to 69 mL/min, or history of serious or frequent infections. The trial excluded patients with AST or ALT ≥2 times the upper limit of normal (ULN) or bilirubin ≥3 times (ULN) and patients requiring a strong CYP3A inhibitor or inducer. SEQUOIA The safety of BRUKINSA monotherapy in patients with previously untreated CLL/SLL was evaluated in a randomized, multicenter, open-label, actively controlled trial [see Clinical Studies (14.4)]. Patients without deletion of chromosome 17p13.1 (17p deletion) (Cohort 1) received either BRUKINSA 160 mg twice daily until disease progression or unacceptable toxicity (n=240) or bendamustine plus rituximab (BR) for 6 cycles (n=227). Bendamustine was dosed at 90 mg/m2/day intravenously on the first 2 days of each cycle, and rituximab was dosed at 375 mg/m2 on day 1 of Cycle 1 and 500 mg/m2 on day 1 of Cycles 2 to 6.

* Includes 3 fatal outcomes. † Includes 2 fatal outcomes. a Musculoskeletal pain: musculoskeletal pain, arthralgia, back pain, pain in extremity, myalgia, neck pain, spinal pain, musculoskeletal discomfort, bone pain. b Upper respiratory tract infection: upper respiratory tract infection, nasopharyngitis, sinusitis, rhinitis, pharyngitis, upper respiratory tract congestion, laryngitis, tonsillitis and upper respiratory tract inflammation, and related terms. c Pneumonia: pneumonia, COVID-19 pneumonia, lower respiratory tract infection, lung infiltration, and related terms including specific types of infection. d Hemorrhage: all terms containing hematoma, hemorrhage, hemorrhagic, and related terms indicative of bleeding. e Includes multiple similar adverse reaction terms. f Rash: Rash, dermatitis, drug eruption, and related terms. g Bruising: all terms containing bruise, bruising, contusion, or ecchymosis. h Fatigue: fatigue, asthenia, and lethargy. i Second primary malignancy: includes non-melanoma skin cancer, malignant solid tumors (including lung, renal, genitourinary, breast, ovarian, and rectal), and chronic myeloid leukemia. j Dizziness: dizziness and vertigo.

Other clinically significant adverse reactions occurring in <10% of BRUKINSA recipients in this cohort included COVID-19 (9%), edema (8%), abdominal pain (8%), urinary tract infection (7%), and atrial fibrillation or flutter (3.3%). Table 10 summarizes select laboratory abnormalities in this cohort. Table 10: Select Laboratory Abnormalities (≥20%) that Worsened from Baseline in Patients with Previously Untreated CLL/SLL without 17p Deletion in SEQUOIA Laboratory Abnormalitya

CLL/SLL without 17p deletion System Organ Class Preferred Term

BRUKINSA (N=240) All Grades Grade 3 or 4 (%) (%)

BR (N=227) All Grades Grade 3 or 4 (%) (%)

Musculoskeletal and connective tissue disorders 33

1.7

0.4

Upper respiratory tract infectionb

1.3

0.9

Pneumoniac

13*

8†

Hemorrhaged

27*

0.4

Hypertensione

2.6

1.3

2.6

Musculoskeletal paina Infections and infestations

Hemoglobin decreased

2.5

Platelets decreased

1.7

Leukocytes increased

21b

0.4

Chemistry abnormalities Glucose increasedc

Creatinine increased

0.8

0.4

Magnesium increased

0.4

Alanine aminotransferase increased

2.1

2.2

The denominator used to calculate the rate was 239 in the BRUKINSA arm and 227 in the BR arm, based on the number of patients with a baseline value and at least one post-treatment value. Grading is based on NCI CTCAE criteria. b Lymphocytes increased in 15%. c Nonfasting conditions. a

Single-Arm Cohort: Previously Untreated CLL/SLL and 17p Deletion In 111 patients with previously untreated, 17p del CLL/SLL, the median age was 70, 71% were male, 95% were White, and 1% were Asian. Most patients (87%) had an ECOG performance status of 0 to 1. The median duration of exposure to BRUKINSA was 30 months. Fatal adverse reactions occurred in 3 (2.7%) patients, including pneumonia, renal insufficiency, and aortic dissection (1 patient each). Serious adverse reactions occurred in 41% of patients treated with BRUKINSA. Serious adverse reactions reported in ≥5% of patients were pneumonia (8%) and second primary malignancy (7%). Adverse reactions led to treatment discontinuation in 5% of patients, dose reduction in 5%, and dose interruption in 51%. The leading causes of dose modification (≥5% of all patients) were pneumonia, neutropenia, second primary malignancy, and diarrhea. Table 11 summarizes select adverse reactions in this cohort. Table 11: Adverse Reactions in ≥10% of Patients with Previously Untreated CLL/SLL and 17p Deletion in SEQUOIA

Vascular disorders

CLL/SLL with 17p Deletion

Skin and subcutaneous tissue disorders Rashf Bruising

Respiratory, thoracic, and mediastinal disorders Coughe

Gastrointestinal disorders

System Organ Class Preferred Term

BRUKINSA (N=111) All Grades Grade 3 or 4 (%) (%)

Infections and infestations Upper respiratory tract infectiona

Pneumoniab

20*

2.7

Musculoskeletal and connective tissue disorders Musculoskeletal painc Skin and subcutaneous tissue disorders

Diarrhea

0.8

12†

0.9

Rashd

Constipation

0.4

Bruisinge

0.9

Nausea

1.3

Vascular disorders Hemorrhagef

4.5

1.3

1.8

Hypertensiong

5.4

General disorders Fatigueh

T:10.5"

Table 9: Adverse Reactions in ≥10% Patients with Previously Untreated CLL/SLL without 17p Deletion in SEQUOIA

Neutrophils decreased

S:10"

Table 9 summarizes select adverse reactions in this randomized cohort.

Hematologic abnormalities

Additionally, the same BRUKINSA regimen was evaluated in 111 patients with previously untreated CLL/SLL with 17p deletion in a non-randomized single arm (Cohort 2). Randomized Cohort: Previously Untreated CLL/SLL without 17p Deletion In patients with previously untreated CLL/SLL without 17p deletion, the median age was 70, 62% were male, 89% were White, 2% were Asian, and 2% were Black. Most patients (93%) had an ECOG performance status of 0 to 1. The median duration of exposure to BRUKINSA was 26 months, with 71% exposed for more than 2 years. Serious adverse reactions occurred in 36% of patients who received BRUKINSA. Serious adverse reactions that occurred in ≥5% of patients were COVID-19, pneumonia, and second primary malignancy (5% each). Fatal adverse reactions occurred in 11 (4.6%) patients with the leading cause of death being COVID-19 (2.1%). Adverse reactions led to permanent discontinuation of BRUKINSA in 8% of patients, dose reduction in 8%, and dose interruption in 46%. The most common adverse reactions leading to permanent discontinuation were second primary malignancy and COVID-19. The leading causes of dose modification (≥5% of all patients) were respiratory infections (COVID-19, pneumonia) and hemorrhage.

BRUKINSA

All Grades (%) Grade 3 or 4 (%) All Grades (%) Grade 3 or 4 (%)

S:7"

Table 11: Adverse Reactions in ≥10% of Patients with Previously Untreated CLL/SLL and 17p Deletion in SEQUOIA (Continued)

Table 13: Adverse Reactions in ≥10% of Patients with Relapsed or Refractory CLL/SLL Who Received BRUKINSA in ALPINE (Continued)

CLL/SLL with 17p Deletion System Organ Class Preferred Term

BRUKINSA (N=111)

System Organ Class Preferred Term

All Grades (%)

Grade 3 or 4 (%)

0.9

Second primary malignancy

†

Grade 3 or 4 (%)

All Grades (%)

Grade 3 or 4 (%)

0.6

Hemorrhagee

24*

2.5

26†

3.7

Rashg

1.2

0.9

Bruisingh

1.5

0.9

0.3

Musculoskeletal paind Vascular disorders

Gastrointestinal disorders Diarrhea

All Grades (%)

Nausea

Hypertensionf

Constipation

Skin and subcutaneous tissue disorders

Abdominal paing

1.8

Respiratory, thoracic, and mediastinal disorders Coughg

Dyspneag

Ibrutinib (N=324)

Musculoskeletal and connective tissue disorders

Neoplasms h

BRUKINSA (N=324)

Gastrointestinal disorders Diarrhea General disorders

General disorders and administration site conditions Fatiguei

Fatiguei

0.9

Respiratory, thoracic, and mediastinal disorders

Nervous system disorders Headache

Coughf

1.8

* Includes 1 fatal outcome. † Includes non-melanoma skin cancer in 13%. a Upper respiratory tract infection: upper respiratory tract infection, nasopharyngitis, sinusitis, rhinitis, pharyngitis, upper respiratory tract congestion, upper respiratory tract inflammation, viral upper respiratory tract infection, and related terms. b Pneumonia: pneumonia, COVID-19 pneumonia, lower respiratory tract infection, and related terms including specific types of infection. c Musculoskeletal pain: musculoskeletal pain, arthralgia, back pain, pain in extremity, myalgia, neck pain, bone pain. d Rash: Rash, dermatitis, toxic skin eruption, and related terms. e Bruising: all terms containing bruise, bruising, contusion, or ecchymosis. f Hemorrhage: all terms containing hematoma, hemorrhage, hemorrhagic, and related terms indicative of bleeding. g Includes multiple similar adverse reaction terms. h Second primary malignancy: includes non-melanoma skin cancer, malignant solid tumors (including bladder, lung, renal, breast, prostate, ovarian, pelvis, and ureter), and malignant melanoma. i Fatigue: fatigue, asthenia, and lethargy.

Nervous system disorders Dizzinessf

Table 12 summarizes select laboratory abnormalities in this cohort.

* Includes fatal outcomes: pneumonia (9 patients), COVID-19 (8 patients), and hemorrhage (1 patient). † Includes fatal outcomes: pneumonia (10 patients), COVID-19 (9 patients), and hemorrhage (2 patients). a Upper respiratory tract infection: upper respiratory tract infection, sinusitis, pharyngitis, rhinitis, nasopharyngitis, laryngitis, tonsillitis, and related terms. b Pneumonia: Pneumonia, COVID-19 pneumonia, lower respiratory tract infection, lung infiltration, and related terms including specific types of infection. c COVID-19: COVID-19, COVID-19 pneumonia, postacute COVID-19 syndrome, SARS-CoV-2 test positive. d Musculoskeletal pain: musculoskeletal pain, arthralgia, back pain, pain in extremity, myalgia, neck pain, spinal pain, bone pain, and musculoskeletal discomfort. e Hemorrhage: all terms containing hematoma, hemorrhage, hemorrhagic, and related terms indicative of bleeding. f Includes multiple similar adverse reaction terms. g Rash: Rash, Dermatitis, and related terms. h Bruising: all terms containing bruise, bruising, contusion, or ecchymosis. i Fatigue: asthenia, fatigue, lethargy.

Table 12: Select Laboratory Abnormalities (≥20%) that Worsened from Baseline in Patients with Previously Untreated CLL/SLL and 17p Deletion in SEQUOIA

Clinically relevant adverse reactions in <10% of patients who received BRUKINSA included urinary tract infection (9%), supraventricular arrhythmias (9%) including atrial fibrillation or flutter (4.6%), abdominal pain (8%), headache (8%), pruritus (6.2%), constipation (5.9%), and edema (4.6%).

Clinically significant adverse reactions occurring in <10% of BRUKINSA recipients in this cohort included urinary tract infection (8%), edema (7%), atrial fibrillation or flutter (4.5%), and COVID-19 (3.6%).

Table 14 summarizes select laboratory abnormalities in ALPINE.

All Grades (%)

Grade 3 or 4 (%)

Neutrophils decreased

19b

Hemoglobin decreased

3.6

Platelets decreased

0.9

Neutrophils decreased

Hemoglobin decreased

3.7

Hematologic abnormalities

Table 14: Select Laboratory Abnormalities (≥20%) that Worsened from Baseline in Patients Who Received BRUKINSA in ALPINE Laboratory Abnormalitya

BRUKINSA

Ibrutinib

All Grades (%) Grade 3 or 4 (%) All Grades (%) Grade 3 or 4 (%)

Hematologic abnormalities

Chemistry abnormalities Glucose increased

Magnesium increased

Lymphocytes increased

Creatinine increased

0.9

Platelets decreased

3.4

Glucose increased

2.8

Creatinine increased

Phosphate decreased

2.5

2.2

Calcium decreased

0.6

Chemistry abnormalities

The denominator used to calculate the rate varied from 110 to 111 based on the number of patients with a baseline value and at least one post-treatment value. Grading is based on NCI CTCAE criteria. b Grade 4, 9%. c Non-fasting conditions. a

ALPINE The safety of BRUKINSA monotherapy was evaluated in patients with previously treated CLL/SLL in a randomized, multicenter, open-label, actively controlled trial [see Clinical Studies (14.4)]. In ALPINE, 324 patients received BRUKINSA monotherapy, 160 mg orally twice daily and 324 patients received ibrutinib monotherapy, 420 mg orally daily until disease progression or unacceptable toxicity. In ALPINE, the median duration of exposure was 24 months for BRUKINSA. Adverse reactions leading to death in the BRUKINSA arm occurred in 24 (7%) patients. Adverse reactions leading to death that occurred in >1% of patients were pneumonia (2.8%) and COVID-19 infection (1.9%). One hundred and four patients in the BRUKINSA arm (32%) reported ≥1 serious adverse reaction. Serious adverse reactions occurring in ≥5% of patients were pneumonia (10%), COVID-19 (7%), and second primary malignancies (5%). Adverse reactions led to treatment discontinuation in 13% of patients, dose reduction in 11%, and dose interruption in 42%. The leading cause of treatment discontinuation was pneumonia. The leading causes of dose modification (≥5% of all patients) were respiratory infections (COVID-19, pneumonia) and neutropenia. Table 13 summarizes select adverse reactions in ALPINE. Table 13: Adverse Reactions in ≥10% of Patients with Relapsed or Refractory CLL/SLL Who Received BRUKINSA in ALPINE BRUKINSA Ibrutinib (N=324) (N=324) System Organ Class Preferred Term All Grades Grade 3 or 4 All Grades Grade 3 or 4 (%) (%) (%) (%) Infections and infestations Upper respiratory tract infectiona

1.2

Pneumoniab

18*

19†

COVID-19

14*

4.6

†

The denominator used to calculate the rate was 321 in the BRUKINSA arm, and varied from 320 to 321 in the ibrutinib arm, based on the number of patients with a baseline value and at least one post-treatment value. Grading is based on NCI CTCAE criteria.

Follicular Lymphoma The safety of BRUKINSA in combination with obinutuzumab was evaluated in 143 adult patients with relapsed or refractory follicular lymphoma (FL) in study BGB-3111-212 (ROSEWOOD), a randomized, multicenter, open-label trial [see Clinical Studies (14.5)]. The trial required an absolute neutrophil count ≥1 × 109/L, platelet count ≥50 × 109/L, and CLcr ≥30 mL/min and excluded patients requiring a strong CYP3A inhibitor or inducer. Patients were randomized to receive either BRUKINSA 160 mg twice daily until disease progression or unacceptable toxicity plus obinutuzumab (n=143) or obinutuzumab monotherapy (n=71). Obinutuzumab was dosed at 1,000 mg intravenously on Days 1, 8, and 15 of Cycle 1; on Day 1 of Cycles 2 to 6; and then every 8 weeks for up to 20 doses. At the discretion of the investigator, obinutuzumab was administered intravenously on Day 1 (100 mg) and on Day 2 (900 mg) of Cycle 1 instead of 1,000 mg on Day 1 of Cycle 1. In patients who received BRUKINSA in combination with obinutuzumab, the median age was 63, 49% were female, 63% were White, and 21% were Asian. Most patients (97%) had an ECOG performance status of 0 to 1. The median duration of BRUKINSA treatment was 12 months, with 24% of patients treated for at least 2 years. Serious adverse reactions occurred in 35% of patients who received BRUKINSA in combination with obinutuzumab. Serious adverse reactions in ≥5% of patients included pneumonia (11%) and COVID-19 (10%). Fatal adverse reactions occurred in 4.2% of patients, with the leading cause of death being COVID-19 (2.1%). Adverse reactions led to permanent discontinuation of BRUKINSA in 17% of patients, dose reduction in 9%, and dose interruption in 40%. Adverse reactions leading to permanent discontinuation in ≥2% of patients were pneumonia, COVID-19, and second primary malignancy. The leading causes of BRUKINSA dosage modification (42% of all patients) were pneumonia, COVID-19, thrombocytopenia, and neutropenia.

S:10"

BRUKINSA

Laboratory Abnormalitya

S:7"

Table 15 summarizes adverse reactions in BGB-3111-212.

7 DRUG INTERACTIONS

Table 15: Adverse Reactions in ≥10% of Patients with Relapsed or Refractory FL Who Received BRUKINSA in Study BGB-3111-212

7.1 Effect of Other Drugs on BRUKINSA

BGB-3111-212 System Organ Class Preferred Term

Moderate and Strong CYP3A Inhibitors

BRUKINSA + Obinutuzumab (N=143)

All Grades Grade 3 or 4 (%) (%) General disorders and administration site conditions Fatiguea,b 27 1.4 Pyrexia 13 0 Musculoskeletal and connective tissue disorders Musculoskeletal paina,c 22 3.5 Vascular disorders Hemorrhagea,d 20 1.4 Gastrointestinal disorders Diarrhea 18 2.8 Constipation 13 0 Abdominal paina 11 2.1 Infections and infestations

Obinutuzumab (N=71) All Grades (%)

Grade 3 or 4 (%)

25 20

1.4 0

1.4

Moderate and Strong CYP3A Inducers Clinical Impact

• Coadministration with a moderate or strong CYP3A inducer decreases zanubrutinib Cmax and AUC [see Clinical Pharmacology (12.3)] which may reduce BRUKINSA efficacy. • Avoid coadministration of BRUKINSA with strong CYP3A inducers [see Dosage and Administration (2.3)]. • Avoid coadministration of BRUKINSA with moderate CYP3A inducers [see Dosage and Administration (2.3)]. If these inducers cannot be avoided, increase BRUKINSA dosage to 320 mg twice daily [see Dosage and Administration (2.3)].

1.4 0 0

8 USE IN SPECIFIC POPULATIONS

Pneumonia *

COVID-19a,*

4.2

Herpes virus infectiong

2.1

1.4

Urinary tract infectionh

1.4

Respiratory, thoracic, and mediastinal disorders Cough

Dyspneaa,*

2.1

Skin and subcutaneous tissue disorders

Table 16: Select Laboratory Abnormalities (≥20%) that Worsened from Baseline in Patients Who Received BRUKINSA in Study BGB-3111-212 BGB-3111-212 Obinutuzumab

BRUKINSA + Obinutuzumab

The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have a background risk of birth defect, loss, or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively. Data Animal Data Embryo-fetal development toxicity studies were conducted in both rats and rabbits. Zanubrutinib was administered orally to pregnant rats during the period of organogenesis at doses of 30, 75, and 150 mg/kg/day. Malformations in the heart (2 or 3-chambered hearts) were noted at all dose levels in the absence of maternal toxicity. The dose of 30 mg/kg/day is approximately 5 times the exposure (AUC) in patients receiving the recommended dose of 160 mg twice daily. Administration of zanubrutinib to pregnant rabbits during the period of organogenesis at 30, 70, and 150 mg/kg/day resulted in postimplantation loss at the highest dose. The dose of 150 mg/kg is approximately 32 times the exposure (AUC) in patients at the recommended dose and was associated with maternal toxicity. In a pre and postnatal developmental toxicity study, zanubrutinib was administered orally to rats at doses of 30, 75, and 150 mg/kg/day from implantation through weaning. The offspring from the middle and high dose groups had decreased body weights preweaning, and all dose groups had adverse ocular findings (e.g., cataract, protruding eye). The dose of 30 mg/kg/day is approximately 5 times the AUC in patients receiving the recommended dose. 8.2 Lactation Risk Summary There are no data on the presence of zanubrutinib or its metabolites in human milk, the effects on the breastfed child, or the effects on milk production. Because of the potential for serious adverse reactions from BRUKINSA in a breastfed child, advise lactating women not to breastfeed during treatment with BRUKINSA and for two weeks following the last dose. 8.3 Females and Males of Reproductive Potential BRUKINSA can cause embryo-fetal harm when administered to pregnant women [see Use in Specific Populations (8.1)].

All Grades (%)

Grade 3 or 4 (%)

All Grades (%)

Grade 3 or 4 (%)

Platelets decreased

Neutrophils decreased

Hemoglobin decreased

0.8

Lymphocytes decreased

Glucose increasedb

Males Advise men to avoid fathering a child while receiving BRUKINSA and for 1 week following the last dose of BRUKINSA.

Alanine aminotransferase increased

Phosphate decreased

0.8

8.4 Pediatric Use Safety and effectiveness of BRUKINSA in pediatric patients have not been established.

Hematologic abnormalities

Chemistry

The denominator used to calculate the rate was 122 in the BRUKINSA + obinutuzumab arm, and varied from 56 to 58 in the obinutuzumab arm, based on the number of patients with a baseline value and at least one post-treatment value. Grading is based on NCI CTCAE criteria. b Nonfasting conditions. a

6.2 Postmarketing Experience The following adverse reactions have been identified during postapproval use of BRUKINSA. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. • Hepatobiliary disorder: drug-induced liver injury Manufactured for: BeiGene USA, Inc. 1840 Gateway Dr., FL 3 San Mateo, CA 94404 BRUKINSA® is a registered trademark owned by BeiGene, Ltd. or its affiliates. © BeiGene, Ltd. 2024 0721-BRU-PRC-027-r3 7/2024

Pregnancy Testing Pregnancy testing is recommended for females of reproductive potential prior to initiating BRUKINSA therapy. Contraception Females Advise female patients of reproductive potential to use effective contraception during treatment with BRUKINSA and for 1 week following the last dose of BRUKINSA. If this drug is used during pregnancy, or if the patient becomes pregnant while taking this drug, the patient should be informed of the potential hazard to a fetus.

8.5 Geriatric Use Of the 1729 patients with MCL, MZL, WM, CLL/SLL, and FL in clinical studies with BRUKINSA, 59% were ≥65 years of age, and 21% were ≥75 years of age. Patients ≥65 years of age had numerically higher rates of Grade 3 or higher adverse reactions and serious adverse reactions (57% and 38%, respectively) than patients <65 years of age (51% and 29%, respectively). No overall differences in effectiveness were observed between younger and older patients. 8.6 Renal Impairment No dosage modification is recommended in patients with mild, moderate, or severe renal impairment (CLcr ≥15 mL/min, estimated by Cockcroft-Gault). Monitor for BRUKINSA adverse reactions in patients on dialysis [see Clinical Pharmacology (12.3)]. 8.7 Hepatic Impairment Dosage modification of BRUKINSA is recommended in patients with severe hepatic impairment [see Dosage and Administration (2.2)]. The safety of BRUKINSA has not been evaluated in patients with severe hepatic impairment. No dosage modification is recommended in patients with mild to moderate hepatic impairment. Monitor for BRUKINSA adverse reactions in patients with hepatic impairment [see Clinical Pharmacology (12.3)].

T:10.5"

Clinically relevant adverse reactions in <10% of patients who received BRUKINSA in combination with obinutuzumab included bruising, edema, pruritus, petechiae, vomiting, headache, arthralgia, hypertension, sepsis, cardiac arrhythmias, renal insufficiency, febrile neutropenia, transaminase elevation, and pneumonitis.

8.1 Pregnancy Risk Summary Based on findings in animals, BRUKINSA can cause fetal harm when administered to pregnant women. There are no available data on BRUKINSA use in pregnant women to evaluate for a drug-associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes. In animal reproduction studies, oral administration of zanubrutinib to pregnant rats during the period of organogenesis was associated with fetal heart malformation at approximately 5-fold human exposures (see Data). Women should be advised to avoid pregnancy while taking BRUKINSA. If BRUKINSA is used during pregnancy, or if the patient becomes pregnant while taking BRUKINSA, the patient should be apprised of the potential hazard to the fetus.

S:10"

* Includes fatal outcomes: COVID-19 (3 patients), pneumonia (2 patients), dyspnea (1 patient). a Includes multiple related terms. b Fatigue: Fatigue, asthenia, and lethargy. c Musculoskeletal pain: Back pain, musculoskeletal pain, musculoskeletal discomfort, noncardiac chest pain, neck pain, pain in extremity, myalgia, spinal pain, bone pain, arthralgia, and related terms. d Hemorrhage: All terms containing hematoma, hemorrhage, hemorrhagic, and related terms indicative of bleeding. e Upper respiratory tract infection: Upper respiratory tract infection, sinusitis, pharyngitis, laryngitis, rhinitis, nasopharyngitis, laryngopharyngitis, tonsillitis bacterial, and related terms. f Pneumonia: Pneumonia, COVID-19 pneumonia, lung infiltration, lung consolidation, and related terms including specific types of infection. g Herpes virus infection: Herpes viral infection, herpes zoster, herpes simplex, herpes simplex reactivation, varicella, and Epstein-Barr viremia. h Urinary tract infection: Urinary tract infection, cystitis, pyelonephritis, and related terms. i Rash: Rash, erythema, dermatitis, drug eruption, skin reaction, and related terms.

Laboratory Abnormalitya

• Reduce BRUKINSA dosage when coadministered with moderate or strong CYP3A inhibitors [see Dosage and Administration (2.3)].

17 9 11 10

Prevention or management

1.4

2.8

Rasha,i

• Coadministration with a moderate or strong CYP3A inhibitor increases zanubrutinib Cmax and AUC [see Clinical Pharmacology (12.3)] which may increase the risk of BRUKINSA toxicities.

Clinical Impact

Prevention or management

Upper respiratory tract infectiona,e a,f,

Table 17: Drug Interactions that Affect Zanubrutinib

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4630

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One benchtop, not a whole lab! No water system, drain or special electrical connected required to operate the Pentra C400 chemistry analyzer. Now you can have the power of a floor model analyzer on the benchtop! The Pentra C400 chemistry system processes up to 420 tests/hr including ISEs and offers routine metabolic assays, TDMs, DAUs and Adulterants, HbA1c and Vitamin D tests. With 40 open channels, you can add much more for a complete menu to meet your practice needs.

RX DAYTONA+ From Randox Laboratories

The RX daytona+ is a fully automated, benchtop, clinical chemistry analyzer capable of performing high quality testing, with a combined throughput of 450 tests per hour, for accurate results you can trust. The most versatile analyzer in its class, the RX daytona+ combines robust hardware and intuitive software with the world leading RX series test menu for unrivaled performance, with direct HbA1c testing capabilities.

RX IMOLA From Randox Laboratories

The RX imola is a cost-effective system that delivers consistent high-quality results. Capable of handling the workload of a medium to high throughout laboratory and a combined throughput of 560 tests per hour, the RX imola provides rapid, comprehensive testing on a small footprint analyzer when it matters most, with direct HbA1c testing capabilities.

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CLIA WAIVED DRIVE IMPROVED PATIENT OUTCOMES WITH REAL-TIME, ACTIONABLE RESULTS! From Siemens Healthineers

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The DCA Vantage® Analyzer is a multi-parameter, point-of-care analyzer for monitoring glycemic control in patients with diabetes and detecting early kidney disease. Benefits of the DCA Vantage System: • CLIA-waived HbA1c test that is IFCC and NGSP-certified • 1 µl finger stick without fasting – HbA1c results in 6 minutes • Random urine sample provides A:C ratio in 7 minutes* • Requires no sample or reagent preparation prior to testing • Sample integrity safeguards *CLIA moderately complex.

NEED MORE CONTROL OVER YOUR POINT-OF-CARE URINALYSIS TESTING PROCESS? From Siemens Healthineers CLINITEK Status ® Connect System simplifies wireless or wired connectivity and testing oversight in point-of-care urinalysis for improved risk management. • Offers flexible connectivity solutions by integrating data directly to the LIS, EMR or via point-of-care data management software solutions • Provides improved POC testing workflow efficiencies when interfaced to leading data management solutions • Minimize transcription errors with the 2-D bar-code scanner • Improves risk management through advanced operator control functions, prevents unauthorized use • Drives compliance across testing sites with programmable QC protocols and QC lockout • Auto-Checks* help to ensure the quality and accuracy of data while facilitating an enhanced interpretation of results. *Only available when using Siemens test strips with IR or color bands

BIOFIRE SPOTFIRE From bioMerieux

bioMérieux knows that an evolving world deserves evolved diagnostics. Our latest innovation, the BIOFIRE® SPOTFIRE® Respiratory Solution, is the first FDA-cleared and CLIA-waived COVID-19 testing solution. The BIOFIRE® SPOTFIRE® System is an easy-to-use system that runs the BIOFIRE® SPOTFIRE® Respiratory (R) Panel. Benefits of the SPOTFIRE Respiratory Solution include: 15 respiratory targets on 1 PCR test with results in about 15 minutes; minimal benchtop space with vertical scalability up to four modules; easy to use with an intuitive user interface.

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ACUCY INFLUENZA A&B TEST From Sekisui Diagnostics

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The Acucy™ Influenza A&B Test is for the rapid, qualitative detection of influenza A and B viral nucleoprotein antigens from both nasal and nasopharyngeal swabs. Utilizing the Acucy™ Reader in either the point-of-care or laboratory setting, workflow flexibility is achieved with both Read Now and Walk Away features. The combination provides clinicians with standardized and definitive result interpretation.

OSOM® BVBLUE® From Sekisui Diagnostics

PRODUCT FOCUS

CLIA WAIVED

The OSOM® BVBLUE® detects elevated vaginal fluid sialidase activity, an enzyme produced by bacterial pathogens associated with bacterial vaginosis including Gardnerella, Bacteroides, Prevotella and Mobiluncus. OSOM® BVBLUE® is more sensitive than Amsel criteria providing physicians with a more accurate diagnosis to treat and minimize serious health consequences such as early spontaneous preterm births and miscarriage.

OSOM® TRICHOMONAS RAPID TEST From Sekisui Diagnostics

The OSOM® Trichomonas Rapid Test is intended for the qualitative detection of Trichomonas vaginalis antigens from vaginal swabs or from the saline solution. The OSOM® Trichomonas Rapid Test is a CLIA-waived rapid test available today. OSOM® Trichomonas is more sensitive than wet mount due to the assay being able to detect viable and non-viable organisms which offers significant benefits to the patient and clinician alike.

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PRODUCT PRODUCTFEATURE FOCUS

CLIA WAIVED OSOM ULTRA PLUS FLU A&B TEST From Sekisui Diagnostics

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Stronger Clinical Performance Takes Lateral Flow Testing To The Next Level. Providing superior rapid results at the point-of-care. Fast, easy, cost effective so you can test and treat in one visit. • High Performance- Equivalent or exceeding the performance of reader devices, without the need for an instrument • Results in 10 minutes • OSOM® Custom Care- Exceptional Support/Training by licensed medical technologists and experienced healthcare professionals • Made in the USA

OSOM® ULTRA STREP A TEST From Sekisui Diagnostics

The OSOM® Ultra Strep A test is a color immunochromatographic assay intended for the qualitative detection of Group A Streptococcus antigen directly from throat swab specimens. Shown to be not statistically different than single swab culture. Sensitivity 95.7% and 100% Specificity. Includes two additional test sticks for External QC. CLIA Waived.

ULTRA HCG COMBO TEST From Sekisui Diagnostics

The OSOM® Ultra hCG Combo test is a simple immunoassay for the qualitative detection of human chorionic gonadotropin (hCG) in serum or urine for the early confirmation of pregnancy. Internal studies have confirmed that the OSOM® Ultra hCG Combo test does not have a false negative result from hCG variants providing physicians with a higher level of confidence.

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FIRST EVER CLIA WAIVED HEMATOLOGY ANALYZER From Sysmex

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Faster test results, clinical decisions and greater practice efficiency are coming to physicians’ offices with the first CLIA-waived CBC analyzer. Hematology diagnostics leader Sysmex is bringing more lab testing to the point of care. One of the most common blood tests can be conducted reliably and accurately on-site, in as few as three minutes. The device’s ease of use and innovative technology means in-house staff can operate it in just a few easy steps, without lengthy certification and training. The new Sysmex XW-100 will improve health care efficiency and patient care.

PRODUCT FOCUS

CLIA WAIVED

COVID-19 TESTING BIOFIRE SPOTFIRE From bioMerieux

WHY COMPROMISE? FAST AND RELIABLE RESULTS ARE NOW DELIVERED AT THE POINT OF CARE. From LumiraDx

Introducing the next generation in point-of-care diagnostics. With a growing menu of tests, LumiraDx uses a simple process that allows for more time with your patients by using microfluidic technology that delivers results in minutes. Learn more about rapid COVID-19 diagnostic solutions for your physician office at LumiraDx.com.

2025 BUYERS GUIDE | 49

PRODUCT PRODUCTFEATURE FOCUS

COVID-19 TESTING SOFIA® 2 FLUORESCENT IMMUNOASSAY ANALYZER AND RAPID DIAGNOSTIC TEST KITS

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From QuidelOrtho

Sofia® 2 Fluorescent Immunoassay Analyzer and Rapid Diagnostic Test Kits Sofia 2 takes rapid testing to a new level. Proven lateral-flow technology and advanced fluorescent chemistry are all integrated into this small benchtop analyzer which can be used in any point-of-care setting. Sofia 2 kits are easy to use and adaptable to any healthcare setting. Excellent performance, objectivity, quality control, LIS capabilities, and an expanding test menu make Sofia 2 the perfect solution for the physician’s office laboratory.

COVID-19 OR FLU? STOP GUESSING. ONE SWAB, ONE TEST, RESULTS IN JUST 10 MINUTES From Sekisui Diagnostics

From only one sample, the OSOM® Flu SARS-CoV-2 Combo Test simultaneously detects and differentiates between COVID-19, Flu A, and Flu B in just 10 minutes, allowing healthcare providers to make more informed decisions when treating patients who are symptomatic with viral infections that have similar symptoms, but different treatment protocols. Designed for point-of-care testing, the OSOM® Flu SARS-CoV-2 Combo Test empowers healthcare providers with the confidence necessary to initiate immediate treatment and isolation protocols at the very first patient visit. This test has not been FDA cleared or approved. It is authorized by FDA under an EUA for use by authorized laboratories. It has been authorized only for the detection of proteins from SARS-CoV-2, influenza A and influenza B, not for any other viruses or pathogens and is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug, and Cosmetic Act, 21 U.S.C S360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.

METRIX® COVID-19 TEST – A MOLECULAR LAB ANYWHERE AND EVERYWHERE From Sekisui Diagnostics

The Metrix® COVID-19 is a novel technology includes clinical claims for symptomatic and asymptomatic individuals, along with dualsample types for nasal or saliva, allowing for an enhanced point-ofcare testing experience. The reader is compact and robust, it’s ideal for professional use in diverse locations, including clinics and mobile health units. It’s a maintenance free device with no calibration step required.

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BE PREPARED FOR RESPIRATORY SEASONS WITH THE OSOM® COVID-19 ANTIGEN RAPID TEST

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From Sekisui Diagnostics The OSOM® COVID-19 Antigen Rapid Test is a lateral flow immunoassay that detects the SARS-CoV-2 nucleocapsid protein with a nasal swab in only 15 minutes at the point-of-care. The test is intended to be used by healthcare professionals or operators on patients suspected of COVID-19 within the first 7 days of symptom onset. The clinical performance compares favorably against polymerase chain reaction methodology, with a positive percent agreement of 95.1% and a negative percent agreement of 97%.

PRODUCT FOCUS

COVID-19 TESTING

OSOM® COVID-19 Antigen Rapid Test has not been FDA cleared or approved. It is authorized by FDA under an EUA for prescription use only. It has been authorized only for the detection of SARS-CoV-2 antigen, not for any other viruses or pathogens and is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug, and Cosmetic Act, 21 U.S.C S360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.

DIABETES/BLOOD GLUCOSE ACCURATE, ACTIONABLE RESULTS FROM THE LEADER IN POINT-OF-CARE LIPID TESTING From Abbott

The CLIA-waived Alere Cholestech LDX™ Analyzer is engineered for confidence, providing accurate, actionable, and readily accessible results that have set the standard in point-of-care lipid profile, cholesterol, and glucose testing. Results are easy to obtain. Fingerstick sampling and a small sample size (40μL) makes results less painful and time consuming.

NOVA PRIMARY BLOOD GLUCOSE REFERENCE ANALYZER From Nova Biomedical

The U.S. FDA has cleared Nova Primary as a blood glucose reference analyzer that fills the need for a new reference analyzer to replace the YSI STAT PLUS 2300 (YSI, Inc., Yellow Springs, OH). Manufacturers of blood glucose measuring devices and clinical diabetes researchers have relied on the YSI 2300 as a reference and correlation analyzer. However, YSI, Inc. no longer supports the analyzer, and its discontinuation has left a critical industry void. With today’s FDA clearance, Nova Primary from Nova Biomedical is now available in the U.S. and worldwide.

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PRODUCT PRODUCTFEATURE FOCUS

DIABETES/BLOOD GLUCOSE QUANTAFLO® PAD From Semler Scientific

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QuantaFlo® PAD is an easy to use, accurate, point of care, non-invasive solution that aids in the early detection of peripheral arterial disease (PAD). This FDA cleared device can be administered by a medical aide in less than 5 minutes. As published in the Journal of Vascular Surgery and the American Journal of Preventive Medicine, QuantaFlo detected undiagnosed PAD in 31.6% of patients +65.1 QuantaFlo is portable and integrates with other technologies and platforms. It is ideal for both home and clinic environments. 1. Smolderen KG, Ameli O, Chaisson CE, Heath K, Mena-Hurtado C. Peripheral Artery Disease Screening in the Community and 1-Year Mortality, Cardiovascular Events, and Adverse Limb Events, AJPM Focus (2022), https://doi.org/10.1016/j.focus.2022.100016

EARLY DETECTION AND MANAGEMENT OF CHRONIC CONDITIONS WITH DCA VANTAGE® AND CLINITEK STATUS®+ ANALYZERS From Siemens Healthineers

Siemens Healthineers DCA Vantage® and CLINITEK Status® family of analyzers provide Hemoglobin A1c (HbA1c) and albumin-to-creatinine ratio (ACR) testing at the point of care. Monitor glycemic control in patients with diabetes and screening for kidney disease in patients at-risk, in-office. Enable real-time consultation, eliminating loss to follow-up. Improve the patient experience and overall outcome by providing actionable results in minutes. CLIA-waived: DCA HbA1c; CLINITEK Microalbumin 2 (ACR) CLIA Moderate Complexity: DCA® Microalbumin/Creatinine (ACR)

FLU AND RESPIRATORY STATUS FLU A&B From LifeSign

Status Flu A & B is an in vitro rapid qualitative test that detects influenza type A and type B directly from nasal swab, nasopharyngeal swab, and nasopharyngeal aspirate/wash specimens obtained from patients with signs and symptoms of respiratory infection. It is intended to aid in the rapid differential diagnosis of Influenza A and B viral infections. • CLIA waived *Innovative flip design with onboard sample extraction • Premeasured developer solution capsule for increased accuracy and ease of use • Flocked nasal swabs for improved patient comfort and superior specimen collection 52 | PHYSICIANS OFFICE RESOURCE

FLU AND RESPIRATORY

From LifeSign

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A Rapid Immunoassay for the Simultaneous Direct Detection and Differential Diagnosis of SARS-CoV-2, Influenza Type A and Type B Antigen from Anterior Nasal and Nasopharyngeal swab specimens. Infections with these viruses may present similar symptoms. Can you tell them apart? WE CAN!

BIOFIRE SPOTFIRE From bioMerieux

PRODUCT FOCUS

STATUS COVID-19/FLU A&B PANEL TEST

bioMérieux knows that an evolving world deserves evolved diagnostics. Our latest innovation, the BIOFIRE® SPOTFIRE® Respiratory Solution, is the first FDA-cleared and CLIA-waived COVID-19 testing solution. The BIOFIRE® SPOTFIRE® System is an easyto-use system that runs the BIOFIRE® SPOTFIRE® Respiratory (R) Panel. Benefits of the SPOTFIRE Respiratory Solution include: 15 respiratory targets on 1 PCR test with results in about 15 minutes; minimal benchtop space with vertical scalability up to four modules; easy to use with an intuitive user interface.

SOFIA® 2 FLUORESCENT IMMUNOASSAY ANALYZER AND RAPID DIAGNOSTIC TEST KITS From QuidelOrtho

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PRODUCT PRODUCTFEATURE FOCUS

FLU AND RESPIRATORY ACUCY INFLUENZA A&B TEST From Sekisui Diagnostics

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The Acucy™ Influenza A&B Test is for the rapid, qualitative detection of influenza A and B viral nucleoprotein antigens from both nasal and nasopharyngeal swabs. Utilizing the Acucy™ Reader in either the point-ofcare or laboratory setting, workflow flexibility is achieved with both Read Now and Walk Away features. The combination provides clinicians with standardized and definitive result interpretation.

COVID-19 OR FLU? STOP GUESSING. ONE SWAB, ONE TEST, RESULTS IN JUST 10 MINUTES From Sekisui Diagnostics

METRIX® COVID-19 TEST – A MOLECULAR LAB ANYWHERE AND EVERYWHERE From Sekisui Diagnostics

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FLU AND RESPIRATORY 4661

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BE PREPARED FOR RESPIRATORY SEASONS WITH THE OSOM® COVID-19 ANTIGEN RAPID TEST

OSOM ULTRA PLUS FLU A&B TEST From Sekisui Diagnostics

OSOM® ULTRA STREP A TEST From Sekisui Diagnostics

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PRODUCT FEATURE

HEMATOLOGY CELL-DYN EMERALD 22 HEMATOLOGY ANALYZER From Abbott

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The CELL-DYN Emerald 22 is a full performance 5-part hematology analyzer for smaller clinical laboratories seeking productivity in smaller spaces. Benefits: • Compact Design - To conserve valuable workspace. • Small and Powerful - Includes a numeric keypad entry, reagent tray, and integrated color touchscreen monitor. • Easy and Automated - Barcoded reagents and touch-free scheduled daily maintenance, startup and shutdown. • Online product training - Self-pace training available 24x7 on the Abbott’s Hematology Academy.

TURN SMALL PLACES INTO SMART SPACES From Abbott

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With reduced budgets, shrinking laboratory space and staffing challenges, many laboratories need a solution that lets them work smarter with less. The CELL-DYN Emerald 22 AL is a full performance, automated optical 5-part differential analyzer that delivers smarter results for small to midsize clinical laboratories. • Compact Design • Walkaway Functionality • Ease Of Use • Smart Safety Features

MICROS HEMATOLOGY ANALYZER WITH 3-PART DIFFERENTIAL PLUS THE LITEDM From HORIBA Medical

Is it viral or bacterial? A CBC with 3-part differential can provide the clues to help distinguish between viral and bacterial infections before you decide to treat. The Micros 60 Hematology analyzer provides a CBC with 3-part Diff result in less than 60 seconds using only 10 µL of sample. Connect to the LiteDM Patient Data Management System for an affordable way to consolidate patient results to one report.

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HEMATOLOGY

From OLO

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OLO® by Sight Diagnostics® is a state-of-the-art benchtop CBC analyzer that leverages AI, spectroscopy, and digital fluorescent microscopy to provide lab-grade results through full blood sample digitization. OLO offers 19 CBC parameters, including a 5-part white blood cell differential and 14 distinct flags. It handles venous and capillary blood samples with a minimum of 27 µL, and is suitable for children as young as three months. OLO’s unique cartridge-based technology, free from liquid reagents, and its internal controls offer easy maintenance, room-temperature storage, reduced operational overhead, and IQCP- eligibility.

PRODUCT FOCUS

STATE-OF-THE-ART BENCHTOP CBC ANALYZER

OLO is FDA 510(k) cleared for use in moderately complex laboratories. For full indications for use and safety information, please refer to the Quality and Compliance page at www.sighdx.com.

HEMATOLOGY TESTING MADE EASY From Sysmex

Designed for labs testing up to 25 samples per day, the Sysmex pocH-100i™ has the smallest footprint of any analyzer on the market. The instrument requires only 15uL of whole blood for reporting of 17 clinical parameters, including a 3-part WBC Differential. It is ideal for urgent care, physician office lab, small clinic, or any outpatient setting where a point of care CBC is needed.

NOW IT’S MORE THANK JUST A BLOOD TEST From Sysmex

With its simplified operation, the Sysmex XP-300™ is ideal for clinics and physician office labs. It provides a CBC with 17 different parameters, including a 3-part WBC Differential. The XP-300+M combines the accuracy and reliability of a Sysmex CBC with the agility of Medicus Middleware. Features include EMR connectivity, instrument interfaces and a QC module.

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PRODUCT FEATURE

HEMATOLOGY FIRST EVER CLIA WAIVED HEMATOLOGY ANALYZER From Sysmex

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LABORATORY SERVICES MEDICUS LIS

From Medicus LIS

If you are considering in-house lab testing, including Covid-19 testing and required reporting to state agencies, connecting Lab to LIS and EHR makes the process of test orders to completed results much easier. Providers receive test results posted to patient charts in real-time, expediting patient care, saving time, money and even preparing for lab test reimbursement goals. Link Your Lab with Medicus LIS today! Contact us: 888-643-8081 sales@medicuslis.com

CLIA COMPLIANT, USER-FRIENDLY, COST-EFFECTIVE, ELECTRONIC DOCUMENTATION SYSTEM From MyInspection

• Meets all CLIA compliance requirements • No interpretation of CLIA regulations required – includes all policies, procedures, electronic fillable forms stored systematically for easy retrieval • Remote access – manage individual or multiple labs remotely from your PC, tablet or phone • Easy to audit and document changes with electronic signatures and dating • Expert guidance from licensure to your customized documentation system • Be, stay compliant and inspection ready – reduce time, cost, and stress

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LIPID TESTING

From Abbott

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PRODUCT FOCUS

ACCURATE, ACTIONABLE RESULTS FROM THE LEADER IN POINT-OF-CARE LIPID TESTING

MULTIPLEX TESTING BIOFIRE SPOTFIRE From bioMerieux

BE PREPARED FOR RESPIRATORY SEASONS WITH THE OSOM® COVID-19 ANTIGEN RAPID TEST From Sekisui Diagnostics The OSOM® COVID-19 Antigen Rapid Test is a lateral flow immunoassay that detects the SARS-CoV-2 nucleocapsid protein with a nasal swab in only 15 minutes at the point-of-care. The test is intended to be used by healthcare professionals or operators on patients suspected of COVID-19 within the first 7 days of symptom onset. The clinical performance compares favorably against polymerase chain reaction methodology, with a positive percent agreement of 95.1% and a negative percent agreement of 97%. OSOM® COVID-19 Antigen Rapid Test has not been FDA cleared or approved. It is authorized by FDA under an EUA for prescription use only. It has been authorized only for the detection of SARS-CoV-2 antigen, not for any other viruses or pathogens and is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug, and Cosmetic Act, 21 U.S.C S360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.

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PRODUCT FEATURE

PERIPHERAL ARTERIAL DISEASE PAD TESTING SYSTEMS IDEAL FOR PRIMARY CARE TO VASCULAR SPECIALISTS from Newman Medical

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QUANTAFLO® PAD From Semler Scientific

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SPIROMETRY MD6300 MICRO SPIROMETER FULL FUNCTION LOW COST SPIROMETER From Mirco Direct

The Micro Spirometer is the newest offering in the Micro Direct spirometer line. Specifically designed for situations where low cost, precision spirometry measurements are required, the Micro Spirometer is lightweight and portable making it suitable for the physician office. The Micro Spirometer features a large color touch screen that is icon driven. The Micro Spirometer is supplied with Device Studio. A PC software for producing printouts of tests results or for creating PDF reports for attachment to the patients’ EMR file.

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SPIROMETRY 4679

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From Micro Direct

The Pneumotrac connects to your PC by USB and captures reliable tests results immediately using the Spirotrac 6 software. These results can be printed or shared easily with compatible EMR systems. The Pneumotrac features a highly accurate, extremely stable Fleisch pneumotrach and meets the latest 2019 ATS/ERS standardization of spirometry ensuring testing meets the most up-to-date guidelines. Real-time curves and new animated incentives encourage maximal patient performance and obtain prompt quality feedback using the latest test session/session acceptability, usability and repeatability criteria.

PRODUCT FOCUS

MD6800 PNEUMOTRAC SPIROMETER A POWERFUL SOLUTION FOR PC-BASED SPIROMETRY

STREP TESTS SOFIA® 2 FLUORESCENT IMMUNOASSAY ANALYZER AND RAPID DIAGNOSTIC TEST KITS From QuidelOrtho

OSOM® ULTRA STREP A TEST From Sekisui Diagnostics

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PRODUCT FEATURE

SYNDROMIC TESTING BIOFIRE® FILMARRAY® TORCH From bioMérieux

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The BIOFIRE® FILMARRAY® TORCH is a fully integrated, random, and continuous-access system designed to meet your laboratory’s syndromic infectious disease testing needs. The benchtop footprint of the BIOFIRE TORCH saves precious lab space, and its scalability meets high throughput demands. BIOFIRE® FILMARRAY® Link Software automatically uploads patient results. Fully compatible with all BIOFIRE® FILMARRAY® Panels intended for use in CLIA-moderate settings, the BIOFIRE TORCH helps you maximize efficiency and productivity.

TOXICOLOGY TOXICOLOGY SCREENING SIMPLIFIED ABBOTT’S IMMTOX 270 BENCHTOP ANALYZER NOW WITH 14 ASSAYS 4683 CLIA CATEGORIZED AS MODERATE COMPLEXITY From Abbott

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TOXICOLOGY URINE DRUG SCREENING REAGENTS From Abbott

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TOXICOLOGY 4685

From Carolina Liquid Chemistries

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Carolina Liquid Chemistries Corp. introduces the Fentanyl Urine Detection Test on CLC’s next-generation RYAN™ immunofluorescent analyzer. This FDA cleared and CLIA categorized, moderately complex, compact, point-of-care system detects fentanyl qualitatively in human urine at a cutoff concentration of 1.0 ng/mL. The test can be run in < 6 minutes, produces a chartable result, and is interfaceable. For detailed information, visit carolinachemistries.com/products/fentanyl-urinedetect-on-clc-ryan-analyzer/.

PRODUCT FOCUS

FIRST EVER FDA-CLEARED AND CATEGORIZED, POINT-OF-CARE FENTANYL TEST (<6 MINUTES)

URINALYSIS EARLY DETECTION AND MANAGEMENT OF CHRONIC CONDITIONS WITH DCA VANTAGE® AND CLINITEK STATUS®+ ANALYZERS

4686

From Siemens Healthineers

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Siemens Healthineers DCA Vantage® and CLINITEK Status® family of analyzers provide Hemoglobin A1c (HbA1c) and albumin-tocreatinine ratio (ACR) testing at the point of care. Monitor glycemic control in patients with diabetes and screening for kidney disease in patients at-risk, in-office. Enable real-time consultation, eliminating loss to follow-up. Improve the patient experience and overall outcome by providing actionable results in minutes. CLIA-waived: DCA HbA1c; CLINITEK Microalbumin 2 (ACR) CLIA Moderate Complexity: DCA® Microalbumin/Creatinine (ACR)

WOMEN'S HEALTH WHY BINDEX® IS A GAME-CHANGER INOSTEOPOROSIS DIAGNOSTICS. From Bindex Medical

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Comparable to DXA Extensive clinical research has proven Bindex to be 90% accurate in detecting osteoporosis. It can replace nearly 70% of DXA scans for patients with suspected osteoporosis. Fast and effective Using safe pulse-echo ultrasound to measure cortical bone thickness, Bindex analyzes bone density in just seconds. Easy to use anywhere Lightweight and pocket-sized, Bindex allows patients to receive on-the-spot bone density scans in doctors’ offices, hospitals and clinics and at home. 2025 BUYERS GUIDE | 63

PRODUCT FEATURE

WOMEN'S HEALTH OSOM® BVBLUE® From Sekisui Diagnostics

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OSOM® TRICHOMONAS RAPID TEST From Sekisui Diagnostics

ULTRA HCG COMBO TEST From Sekisui Diagnostics

64 | PHYSICIANS OFFICE RESOURCE

9 TRAVEL DESTINATIONS YOU CAN'T MISS IN 2025

Whether you're craving pristine beaches or vibrant cities, these nine must-visit destinations around the world promise stunning scenery, rich culture, and unforgettable adventures for every type of traveler. HARBOUR VILLAGE BEACH CLUB · TURTLE BAY RESORT · FOUR SEASON ORLANDO AT WALT DISNEY WORLD · SECRETS CAP CANA · BALBOA BAY RESORT · DESOLATION HOTEL THE TAMPA EDITION HOTEL · FOUR SEASONS NASHVILLE · FOUR SEASONS LAS VEGAS

MD-ESCAPES.COM 2025 BUYERS GUIDE | 65

HARBOUR VILLAGE BEACH CLUB

HARBOUR VILLAGE BEACH CLUB BONAIRE, CARIBBEAN Tucked away on a private stretch of white sand and palm trees, you will find the iconic Harbour Village Beach Club. An oasis beloved by sun lovers, scuba divers, and seafarers alike. Our boutique Bonaire retreat captures the breezy, barefoot elegance of the Dutch Caribbean, consistently earning the title of “Bonaire's leading hotel” in the World Travel Awards.

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TURTLE BAY RESORT OAHU, HAWAII Deeply rooted in the land, the history, and the layered richness of Oahu, at Turtle Bay you’ll find an authentic connection to a place of uncommon natural splendor and the warm, welcoming community within it. Where your days are filled with constant discovery and moments that touch your soul, allowing you to explore the uncommon depths of this remarkable coast.

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FOUR SEASON ORLANDO AT WALT DISNEY WORLD ORLANDO, FLORIDA Discover an elevated escape with the perfect balance of fun and relaxation at our AAA Five Diamond, luxury Orlando Resort. Splash around with the family at Explorer Island water park, or unwind beneath swaying palms at Oasis adult-only pool while we entertain your young ones at our complimentary kids camp. Treat yourself to a soothing, post-park massage at The Spa, then toast to the nightly Walt Disney World® fireworks views over dinner at our Michelin-starred rooftop steakhouse Capa.

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FOUR SEASONS ORLANDO AT WALT DISNEY WORLD

SECRETS CAP CANA PUNTA CANA DOMINICAN REPUBLIC Secrets Cap Cana Resort & Spa is a sophisticated, adults-only hideaway located in the exclusive gated community of Cap Cana Facing the clear Caribbean Sea along the white sand of the exclusive Juanillo Beach. Secrets Cap Cana Resort & Spa is proud to support the Punta Cana Promise as part of the ongoing commitment to ensure that guests will continue to receive the highest levels of service and security they have come to know and expect from Secrets Cap Cana. The Punta Cana Promise reaffirms the commitment to a set of security standards and safety guidelines in one of the top travel destinations in the Dominican Republic.

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BALBOA BAY RESORT NEWPORT BEACH , CALIFORNIA Balboa Bay Resort is Newport Beach’s premier waterfront retreat offering stunning bay views and sunsets over Balboa Bay’s harbor. It is the #1 Resort in Newport Beach per U.S. News & World Report, and it is rated as a Forbes Four-Star and AAA Four-Diamond resort.

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TURTLE BAY RESORT

DESOLATION HOTEL LAKE TAHOE, CALIFONIA At Desolation Hotel, modern conveniences and eco-luxury commingle with Japanese tranquility and Scandinavian design. Our one-of-a-kind South Lake Tahoe experience inspires adventure and invites tranquility, providing the right space to recharge your battery. Balancing reverence for the past with appreciation for the present, Desolation Hotel nods to the simple days of yesteryear, while modern technology serves as a quiet backbone to the entire resort experience.

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THE TAMPA EDITION HOTEL

THE TAMPA EDITION HOTEL TAMPA, FLORIDA Situated within the new 56-acre Water Street Tampa neighborhood, the hotel is home to 172 guest rooms and suites and 7 food and beverage venues, including a signature restaurant, rooftop bar and terrace. The property features a 204 sqm Penthouse Suite, expansive spa, fitness center and over 550 sqm of flexible meeting and events space. Bringing some of the world’s best talents together into one project, the property is designed by acclaimed New York-based architecture practice Morris Adjmi in collaboration with Florida-based firm Nichols Brosch Wurst Wolfe & Associates; with interiors designed by the renowned Roman & Williams, and the whole project underpinned by the creative vision of Ian Schrager and Ian Schrager Company.

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FOUR SEASONS NASHVILLE, TENNESSEE Welcome to Four Seasons Hotel Nashville, a luxury hotel located in the heart of downtown’s vibrant SoBro neighborhood. This new social hub is just steps away from the city's iconic music, sports, and entertainment venues. Experience the rhythm of our lively restaurants and event spaces, the tranquility of our Spa, and the stunning views from our rooftop pool overlooking the Cumberland River and Riverfront Park. With the unmatched service of Four Seasons and warm Southern hospitality, we’ll inspire an authentic experience of Music City.

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FOUR SEASONS LAS VEGAS

FOUR SEASONS LAS VEGAS, NEVADA As one of the only non-gaming and non-smoking hotels on The Strip, Four Seasons Hotel Las Vegas is a unique oasis in the heart of the action-packed sports and entertainment capital of the world. Offering Five Diamond luxury accommodations, acclaimed dining and a Forbes Five-Star spa, Four Seasons offers the best of both worlds: a resort retreat amid the famous energy of Las Vegas.

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THE POWER TO DETECT THE HIDDEN THREAT OF PERIPHERAL ARTERIAL DISEASE (PAD) 4691

“PAD IS ASYMPTOMATIC IN 75% OF ELDERLY PATIENTS.” 1

IN PRIMARY CARE: “THE RISK OF MORTALITY WAS SIMILAR IN SYMPTOMATIC AND ASYMPTOMATIC PATIENTS WITH PAD” 2

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1. Sillesen, H., & Falk, E. (2011). Peripheral artery disease (PAD) screening in the asymptomatic population: why, how, and who?. Current atherosclerosis reports, 13(5), 390–395. https://doi.org/10.1007/s11883-011-0196-x 2. Diehm, C., Allenberg, J. R., Pittrow, D., Mahn, M., Tepohl, G., Haberl, R. L., Darius, H., Burghaus, I., Trampisch, H. J., & German Epidemiological Trial on Ankle Brachial Index Study Group (2009). Mortality and vascular morbidity in older adults with asymptomatic versus symptomatic peripheral artery disease. Circulation, 120(21), 2053–2061. https://doi.org/10.1161/CIRCULATIONAHA.109.865600 ML00190 Rev A

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The Aptitude Metrix® COVID-19 Test is provided by SEKISUI Diagnostics The Metrix COVID-19, OSOM COVID-19 Antigen Rapid Test, and OSOM Flu SARS-CoV-2 Combo Test have not been FDA cleared or approved. They are authorized by FDA under an EUA for use by authorized laboratories. The Metrix COVID-19 has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens. The OSOM COVID-19 Antigen Rapid Test has been authorized only for the detection of SARS-CoV-2 antigen, not for any other viruses or pathogens. OSOM Flu SARS-CoV-2 Combo Test has been authorized only for the detection of proteins from SARS-CoV-2, influenza A and influenza B, not for any other viruses or pathogens. The use of these products are only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug, and Cosmetic Act, 21 U.S.C S360bbb-3(b)(1), unless the authorization is terminated or revoked sooner. © 2024 SEKISUI Diagnostics, LLC. All rights reserved. OSOM® is a registered trademark of SEKISUI Diagnostics, LLC. Because every result matters™ is a trademark of SEKISUI Diagnostics, LLC. Metrix® is a registered trademark of Aptitude Medical Systems Inc.