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Study breakdown

Semaglutide Drug Safety Signals: Global Pharmacovigilance Analysis

CohortModerate evidence
The takeaway

Descriptive analysis from VigiAccess global pharmacovigilance database characterizes drug-related problems associated with semaglutide across international reporting systems.

Key finding

Descriptive analysis from VigiAccess global pharmacovigilance database characterizes drug-related pr

What the researchers found

Descriptive analysis from VigiAccess global pharmacovigilance database characterizes drug-related problems associated with semaglutide across international reporting systems.

Why it matters

Relevant to peptide therapeutics.

The numbers in context

Six GLP-1 drugs analyzed: exenatide, lixisenatide, liraglutide, dulaglutide, semaglutide, and tirzepatide from the WHO VigiAccess database.

How the study worked

In publication.

Who was studied

Global pharmacovigilance reports for six GLP-1 drugs from the WHO VigiAccess database

What this study cannot tell us

In publication.

How to read the evidence

Based on design.

When this study was published

Published in 2025.

The bigger picture

Advances peptide evidence.

Questions still open

  • Long-term implications?
  • Evidence comparison?
  • Next steps?

Common questions

What does this mean?
Descriptive analysis from VigiAccess global pharmacovigilance database characterizes drug-related problems associated with semaglutide across international reporting systems.
How reliable?
Consult publication.

Read the original research

A Descriptive Analysis from VigiAccess on Drug-related Problems Associated with the Glucagon-like Peptide-1 Receptor Agonists.

Current drug safety

Citation

Amirthalingam, Palanisamy. (2025). A Descriptive Analysis from VigiAccess on Drug-related Problems Associated with the Glucagon-like Peptide-1 Receptor Agonists.. Current drug safety. https://doi.org/10.2174/0115748863367086250420011411