Tirzepatide Real-World Safety: FAERS Database Analysis of Adverse Events

Retrospective analysis of FDA FAERS data identifies real-world safety concerns with tirzepatide beyond clinical trial reporting, including GI events and hypoglycemia patterns.

Almansour, Hadi A et al.·Healthcare (Basel·2025·Moderate Evidencecohort
RPEP-09881CohortModerate Evidence2025RETHINKTHC RESEARCH DATABASErethinkthc.com/research

Quick Facts

Study Type
cohort
Evidence
Moderate Evidence
Sample
N=large
Participants
Patients with reported adverse events from tirzepatide in the FDA FAERS database (2022-2025)

What This Study Found

Retrospective analysis of FDA FAERS data identifies real-world safety concerns with tirzepatide beyond clinical trial reporting, including GI events and hypoglycemia patterns.

Key Numbers

FAERS reports from 2022 to Q1 2025 analyzed using proportional reporting ratio and related disproportionality methods.

How They Did This

Methodology detailed in publication.

Why This Research Matters

Relevant to expanding peptide-based therapeutic applications.

The Bigger Picture

Contributes to the growing evidence for peptide therapeutics.

What This Study Doesn't Tell Us

Limitations in publication.

Questions This Raises

  • ?Long-term implications?
  • ?Comparison to existing evidence?
  • ?Next research steps?

Trust & Context

Key Stat:
Key finding Retrospective analysis of FDA FAERS data identifies real-world safety concerns with tirzepatide beyo
Evidence Grade:
Based on study design in publication.
Study Age:
Published in 2025.
Original Title:
Real-World Safety Concerns of Tirzepatide: A Retrospective Analysis of FAERS Data (2022-2025).
Published In:
Healthcare (Basel, Switzerland), 13(18) (2025)
Database ID:
RPEP-09881

Evidence Hierarchy

Meta-Analysis / Systematic Review
Randomized Controlled Trial
Cohort / Case-Control
Cross-Sectional / ObservationalSnapshot without intervening
This study
Case Report / Animal Study
What do these levels mean? →

Frequently Asked Questions

What does this mean?

Retrospective analysis of FDA FAERS data identifies real-world safety concerns with tirzepatide beyond clinical trial reporting, including GI events and hypoglycemia patterns.

How reliable?

Consult publication and healthcare provider.

Read More on RethinkPeptides

Cite This Study

RPEP-09881·https://rethinkpeptides.com/research/RPEP-09881

APA

Almansour, Hadi A; Thaibah, Hilal A; Alfarhan, Moaddey; Al-Qahtani, Saeed A; Khardali, Amani A; Alshammari, Thamir M. (2025). Real-World Safety Concerns of Tirzepatide: A Retrospective Analysis of FAERS Data (2022-2025).. Healthcare (Basel, Switzerland), 13(18). https://doi.org/10.3390/healthcare13182259

MLA

Almansour, Hadi A, et al. "Real-World Safety Concerns of Tirzepatide: A Retrospective Analysis of FAERS Data (2022-2025).." Healthcare (Basel, 2025. https://doi.org/10.3390/healthcare13182259

RethinkPeptides

RethinkPeptides Research Database. "Real-World Safety Concerns of Tirzepatide: A Retrospective A..." RPEP-09881. Retrieved from https://rethinkpeptides.com/research/almansour-2025-realworld-safety-concerns-of

Access the Original Study

Study data sourced from PubMed, a service of the U.S. National Library of Medicine, National Institutes of Health.

This study breakdown was produced by the RethinkPeptides research team. We analyze and report published research findings without making health recommendations. All interpretations are based solely on the published abstract and study data.