How Do I Report GLP-1 Side Effects to the FDA?
Last updated: January 2026
Quick Answer
Use the FDA MedWatch program online at fda.gov/medwatch or call 1-800-FDA-1088. Reporting helps track medication safety for all patients.
How Do I Report GLP-1 Side Effects to the FDA
Use the FDA MedWatch program online at fda.gov/medwatch or call 1-800-FDA-1088. Reporting helps track medication safety for all patients.
Safety is the most important consideration when starting any medication. GLP-1 medications have been extensively studied in clinical trials involving tens of thousands of patients, and they have a well-established safety profile when prescribed and monitored by licensed healthcare providers.
What the Research Shows
The STEP and SURMOUNT clinical trial programs included over 25,000 participants combined. These large-scale studies established the efficacy and safety profile that led to FDA approval for weight management.
Staying Safe on GLP-1 Treatment
- Only obtain GLP-1 medications through licensed healthcare providers and pharmacies
- Follow your prescribed dosing schedule and titration plan
- Report any unusual symptoms to your provider promptly
- Attend regular follow-up appointments for monitoring
- Inform all your healthcare providers that you take GLP-1 medications
- Keep medications stored properly and check expiration dates
Related Questions
When Should I Call My Doctor About GLP-1 Side Effects?
Seek immediate care for severe abdominal pain, inability to keep fluids down for 24+ hours, signs of allergic reaction, or severe dehydration.
What FDA Warnings Exist for GLP-1 Medications?
GLP-1 medications carry a black box warning for thyroid C-cell tumors (based on rodent studies) and warnings about pancreatitis, gallbladder disease, and kidney problems.