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FDA Data · GLP-1/GIP

Mounjaro Reported Side Effects

tirzepatide by Eli Lilly. Approved 2022 for type 2 diabetes.

79,973 total adverse event reports in FAERS

What are the most reported side effects of Mounjaro?

These are the 15 most frequently reported adverse events for Mounjaro in the FDA FAERS database. Higher counts mean more reports, not necessarily higher risk.

Injection Site Pain
8,545
Nausea
8,226
Extra Dose Administered
4,782
Diarrhea
4,775
Vomiting
4,137
Injection Site Haemorrhage
3,319
Constipation
2,901
Injection Site Erythema
2,804
Blood Glucose Increased
2,555
Decreased Appetite
2,042
Fatigue
2,025
Accidental Underdose
1,953
Injection Site Bruising
1,886
Weight Loss
1,754
Upper Abdominal Pain
1,726

Side Effects by Category

Other24 reported side effects
Injection Site Pain8,545
Extra Dose Administered4,782
Injection Site Haemorrhage3,319
Injection Site Erythema2,804
Blood Glucose Increased2,555
Accidental Underdose1,953
Injection Site Bruising1,886
Injection Site Pruritus1,467
Illness1,453
Accidental Overdose1,307
Inappropriate Schedule Of Product Administration1,238
Weight Increased1,231
Abdominal Discomfort1,147
Injection Site Mass1,138
Pain888
Injection Site Swelling883
Gastrointestinal Disorder863
Blood Glucose Decreased849
Injection Site Reaction785
Feeling Abnormal780
Injection Site Injury780
Injection Site Rash779
Product Administered At Inappropriate Site726
Hunger722
Digestive12 reported side effects
Nausea8,226
Diarrhea4,775
Vomiting4,137
Constipation2,901
Upper Abdominal Pain1,726
Abdominal Pain1,476
Burping (Eructation)1,361
Indigestion1,185
Delayed Stomach Emptying1,108
Pancreatitis875
Bloating787
Flatulence769
Metabolic6 reported side effects
Decreased Appetite2,042
Fatigue2,025
Weight Loss1,754
Dehydration1,132
Malaise844
Weakness778
Neurological2 reported side effects
Headache1,633
Dizziness1,429
Skin & Hair1 reported side effects
Hair Loss849
Mental Health1 reported side effects
Anxiety764

How does Mounjaro compare to other GLP-1 medications?

Frequently Asked Questions

Important: This data comes from the FDA Adverse Event Reporting System (FAERS), a voluntary reporting system. Report counts do not prove the medication caused the event. Not all adverse events are reported, and reporting rates vary by drug, time since approval, and media attention. This tool is for educational purposes only and is not medical advice. Always consult your healthcare provider about medication side effects.

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