• FDA APPROVAL DATE: 12/05/2017
  • CLINICALLY IMPORTANT, POTENTIALLY HAZARDOUS INTERACTIONS WITH:
    Insulin, insulin secretagogues
  • PREGNANCY: Discontinue semaglutide in women at least 2 months before a planned pregnancy due to the long washout period for this drug.

Not indicated for use in type 1 diabetes mellitus or for the treatment of diabetic ketoacidosis.
Semaglutide causes a delay of gastric emptying, and thereby has the potential to impact the absorption of concomitantly administered oral medications.

WARNING: RISK OF THYROID C-CELL TUMORS

IN RODENTS, SEMAGLUTIDE CAUSES THYROID C-CELL TUMORS. IT IS UNKNOWN WHETHER SEMAGLUTIDE CAUSES THYROID C-CELL TUMORS, INCLUDING MEDULLARY THYROID CARCINOMA (MTC), IN HUMANS AS THE HUMAN RELEVANCE OF SEMAGLUTIDE-INDUCED RODENT THYROID C-CELL TUMORS HAS NOT BEEN DETERMINED. SEMAGLUTIDE  IS CONTRAINDICATED IN PATIENTS WITH A PERSONAL OR FAMILY HISTORY OF MTC OR IN PATIENTS WITH MULTIPLE ENDOCRINE NEOPLASIA SYNDROME TYPE 2. COUNSEL PATIENTS REGARDING THE POTENTIAL RISK OF MTC AND SYMPTOMS OF THYROID TUMORS.

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    DRUG REVIEW ARTICLE

    DRUG REVIEW ARTICLE #2

    Click on the DRUG REVIEW ARTICLE links (above) to see two reviews of semaglutide in the Taylor & Francis journal Expert Opinion on Drug Safety.

    (Note that non-subscribers to the journal will only be able to see an abstract of the article.)

Page last updated 05/27/2025

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Incidence

<1% 1‑5% 5‑10% 10‑15% 15‑20% 20‑30% >30%

Seriousness

Hospitalization possible
Life threatening
Fatal

Warnings in other populations

BreastfeedingBreast feeding

GeriatricGeriatric

PediatricPediatric