Acute pancreatitis associated with liraglutide.
Ann Pharmacother · 2011
Last updated 2026-05-28A 60-year-old woman with type 2 diabetes developed severe mid-abdominal pain three weeks after switching from one GLP-1 drug (exenatide) to another (liraglutide). Her blood test showed high lipase levels, a sign of pancreatitis. After stopping liraglutide and receiving standard treatment, her pain and lipase levels improved within four days, and she was discharged from the hospital.
AI summary of the abstract below.
| Journal | Ann Pharmacother, 2011 |
|---|---|
| Citations | 41 |
| Relative citation ratio | 1.23 |
| NIH percentile | 58 |
| Molecules | liraglutide |
Abstract
OBJECTIVE: To report what is, to our knowledge, the first postmarketing case of acute pancreatitis associated with liraglutide.
CASE SUMMARY: A 60-year-old female with type 2 diabetes presented with a 16-hour history of mid-epigastric pain 3 weeks after treatment was changed from exenatide 10 μg twice daily, which she had taken for 4 years, to liraglutide 1.8 mg daily. Her serum lipase level was elevated (478 units/L) at admission, and other laboratory values were within normal limits. Liraglutide was discontinued at admission. Standard therapy for pancreatitis resulted in symptom resolution and a significant decrease in serum lipase (131 units/L) by hospital day 4; she was discharged on hospital day 5.
DISCUSSION: Based on the Naranjo scale, this case represents a probable adverse drug reaction. Eight cases of pancreatitis were observed in liraglutide-treated patients in premarketing clinical trials. Extensive literature describing exenatide-related pancreatitis and premarketing reports of liraglutide-related pancreatitis, along with the temporal relationship between the initiation of liraglutide and the onset of this patient's symptoms, suggest that the episode of pancreatitis was induced by liraglutide.
CONCLUSIONS: Liraglutide should be used cautiously in patients with a history of pancreatitis, and clinicians should have a high index of suspicion for this rare, but potentially serious, adverse effect.
Verbatim abstract via PubMed 21487080 ↗
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