Products - Merck Connect

PIFELTRO™ (doravirine 100 mg) tablets and DELSTRIGO™ (doravirine 100 mg/lamivudine 300 mg/tenofovir disoproxil fumarate 300 mg) tablets Before prescribing PIFELTRO, please read the accompanying Prescribing Information.

Actived: Thursday Feb 25, 2021


Samples, Vouchers, and Coupons for JANUMET® (sitagliptin

Health Care Professionals may request available samples, vouchers, and/or coupons for JANUMET® (sitagliptin and metformin HCl) and JANUMET® XR (sitagliptin and metformin HCl extended-release) for use with their appropriate patients.

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Samples and Coupons for SIVEXTRO® (tedizolid phosphate)

Samples, Vouchers & Coupons. Samples: Receive a 200 mg sample tablet of SIVEXTRO. A 1-tablet (200 mg) package sample of SIVEXTRO is available for your appropriate patients with ABSSSI. If you would like to receive samples of SIVEXTRO, additional product information, or professional support, contact the Merck National Center. Merck National Center

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Efficacy of NEXPLANON® (etonogestrel implant) 68 mg

Indication NEXPLANON is indicated for use by women to prevent pregnancy. Selected Safety Information Contraindications. NEXPLANON should not be used in women who have known or suspected pregnancy; current or past history of thrombosis or thromboembolic disorders; liver tumors, benign or malignant, or active liver disease; undiagnosed abnormal genital bleeding; known or suspected breast cancer

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General Dosing Information

Dosing General dosing information 25-IU dosage increment. Not actual size. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

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Review Patient Resources for JANUVIA® (sitagliptin)

Download patient resources for JANUVIA® (sitagliptin) such as savings information resource for eligible, privately insured patients and a balanced diet guide for healthy eating and portion control.

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The Follistim Pen - Merck Connect

CONTRAINDICATIONS. FOLLISTIM AQ Cartridge is contraindicated in women who exhibit any of the following: prior hypersensitivity to recombinant human follicle-stimulating hormone (hFSH) products; high levels of FSH indicating primary gonadal failure; presence of uncontrolled non-gonadal endocrinopathies (eg, thyroid, adrenal, or pituitary disorders); hypersensitivity reactions to streptomycin or

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Bleeding Pattern Changes and NEXPLANON® (etonogestrel

Total days of spotting or bleeding Percentage of women; Treatment days 91–190 (N=745) Treatment days 271–360 (N=657) Treatment days 631–720 (N=547)

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Insertion and Removal for NEXPLANON® (etonogestrel implant

Insertion time. In a clinical trial, mean insertion time was <1 minute (27.9 ± 29.3 seconds). Insertion time was measured from the removal of the protective cap of the applicator until the retraction of the needle from the arm.

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Dosing for BRIDION® (sugammadex) | Official Site

BRIDION is contraindicated in patients with known hypersensitivity to sugammadex or any of its components. Hypersensitivity reactions that occurred varied from isolated skin reactions to serious systemic reactions (i.e., anaphylaxis, anaphylactic shock) and have occurred in patients with no prior exposure to sugammadex.

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