Key result
Standard-dose paroxetine may induce acute pancreatitis that resolves upon drug cessation.
Why the study?
Evidence linking the selective serotonin reuptake inhibitor paroxetine to acute pancreatitis remains sparse.
Does paroxetine induce acute pancreatitis in patients lacking traditional risk factors?
Does paroxetine induce acute pancreatitis in patients lacking traditional risk factors?
Paroxetine may induce acute pancreatitis even at standard doses, highlighting the need to consider drug-induced pancreatitis in patients lacking traditional risk factors.
May warrant considering paroxetine in unexplained pancreatitis; leaves open confirmation via larger pharmacovigilance studies.
Background Acute pancreatitis (AP) incidence is ~76.2 per 100,000. Drug-induced pancreatitis (DIP) accounts for <2%, yet >500 drugs are implicated. Evidence linking the SSRI paroxetine to AP remains sparse. Case presentation A 28-year-old woman with severe depression self-initiated paroxetine 20 mg once daily; within 24 h she developed persistent epigastric pain and bloating. After brief relief with intravenous fluids she re-administered the same dose, and symptoms recurred within 24 h. Labs showed elevated pancreatic enzymes and CRP. CT revealed mild pancreatitis. No alcohol, hyperlipidemia or other classic risk factors were identified. Paroxetine was immediately discontinued; supportive care led to symptom and enzyme normalization within 72 h. She was discharged on trazodone and remains recurrence-free. Discussion Population studies have not established a significant SSRI–AP association, probably because of the extreme rarity of such events (<0.01%). The positive rechallenge observed here provides robust individual-level evidence of causality, supported by formal probability scales and international criteria. SSRIs may precipitate AP through serotonin-mediated β -cell dysfunction, oxidative stress, or idiosyncratic hypersensitivity. Early recognition is critical because DIP is usually reversible after drug withdrawal. Conclusion This case suggests that paroxetine may induce AP even at standard doses. Clinicians should consider DIP in patients lacking traditional risk factors, especially after self-rechallenge. Early recognition, immediate drug cessation and supportive therapy ensure excellent recovery.
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Wu et al. (2026) studied this question. Paroxetine may induce acute pancreatitis in a 28-year-old woman even at standard doses, with symptoms resolving after drug cessation.
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