• FDA APPROVAL DATE: 05/13/2022
  • CLINICALLY IMPORTANT, POTENTIALLY HAZARDOUS INTERACTIONS WITH:
    Tirzepatide delays gastric emptying and has the potential to impact the absorption of concomitantly administered oral medications.
  • PREGNANCY: Available data with tirzepatide use in pregnant women are insufficient to evaluate for a drug-related risk of major birth defects, miscarriage, or other adverse maternal or fetal outcomes.

Tirzepatide Is not indicated for use in patients with type 1 diabetes mellitus.

WARNING: RISK OF THYROID C-CELL TUMORS

TIRZEPATIDE CAUSES THYROID C-CELL TUMORS IN RATS. IT IS UNKNOWN WHETHER TIRZEPATIDE  CAUSES THYROID C-CELL TUMORS, INCLUDING MEDULLARY THYROID CARCINOMA, IN HUMANS AS THE HUMAN RELEVANCE OF TIRZEPATIDE-INDUCED RODENT THYROID C-CELL TUMORS HAS NOT BEEN DETERMINED.

TIRZEPATIDE IS CONTRAINDICATED IN PATIENTS WITH A PERSONAL OR FAMILY HISTORY OF MEDULLARY THYROID CARCINOMA IN PATIENTS WITH MULTIPLE ENDOCRINE NEOPLASIA SYNDROME TYPE 2. COUNSEL PATIENTS REGARDING THE POTENTIAL RISK OF MEDULLARY THYROID CARCINOMA AND SYMPTOMS OF THYROID TUMORS.

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    DRUG REVIEW ARTICLE

    Click on the DRUG REVIEW ARTICLE tab (above) to see a review of tirzepatide 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 07/22/2025

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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