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Mesalazine-Induced Acute Pancreatitis in Inflammatory Bowel Disease Patients: A Systematic Review
1Department of Pharmacy, Liuyang Hospital of Traditional Chinese Medicine, Changsha, Hunan, 410300, People's Republic of China.
Objective:
Mesalazine is a widely used medication for treating mild to moderate inflammatory bowel disease (IBD). First identified as a potential cause of acute pancreatitis (AP) in 1989, the link between mesalazine and AP has primarily been established through case reports and a limited number of retrospective studies. This study aims to explore the characteristics of mesalazine-induced AP.
Methods:
The databases of CNKI, Wanfang Data, VIP, PubMed and Web of Science were searched (up to March, 2024), and the case reports of mesalazine-related AP in IBD patients were collected and descriptively analyzed.
Results:
Thirty-four reports were included, describing 42 patients (22 males, 16 females, 4 unspecified) with mesalazine-related AP. The onset of pancreatitis occurred a median of 14 days (range 1-730 days) after starting mesalazine. Common symptoms included abdominal pain (100%), vomiting (38.1%), fever (21.4%), and nausea (21.4%). Most patients had elevated serum amylase and lipase levels, with some showing raised C-reactive protein and erythrocyte sedimentation rate. Imaging tests, such as computed tomography and B-scan ultrasonography, revealed edematous infiltration and inflammation. Discontinuation of mesalazine led to symptom resolution in all patients, with 93.3% improving within a week. Alternative treatments or switching to other forms of 5-aminosalicylic acid may be considered for ongoing management. Rechallenge with mesalazine led to recurrence of AP in 21 cases, with a shorter median time to symptom onset.
Conclusion:
Mesalazine-induced AP is a rare but significant adverse reaction, not related to drug dosage, and can occur at any point during treatment, typically within two weeks. The reaction can recur upon rechallenge. Discontinuation of mesalazine and symptomatic treatment typically resolves the condition.
Insights
Mesalazine can cause acute pancreatitis (AP) in inflammatory bowel disease (IBD) patients, often within two weeks. Stopping the drug usually resolves symptoms, but the reaction can recur if mesalazine is reintroduced.
Area of Science:
- Gastroenterology
- Pharmacology
- Clinical Medicine
Background:
- Mesalazine is a primary treatment for inflammatory bowel disease (IBD).
- Acute pancreatitis (AP) is a rare but recognized adverse effect of mesalazine, first reported in 1989.
- Previous evidence linking mesalazine to AP relies on case reports and limited retrospective studies.
Purpose of the Study:
- To investigate the characteristics of acute pancreatitis (AP) induced by mesalazine in patients with inflammatory bowel disease (IBD).
- To analyze the clinical presentation, diagnostic findings, and outcomes of mesalazine-induced AP.
- To evaluate the recurrence risk of AP upon mesalazine rechallenge.
Main Methods:
- A systematic literature search was conducted across multiple databases (CNKI, Wanfang Data, VIP, PubMed, Web of Science) up to March 2024.
- Case reports of mesalazine-related AP in IBD patients were collected.
- Descriptive analysis of the collected case reports was performed.
Main Results:
- The study analyzed 34 reports involving 42 patients with mesalazine-induced AP.
- Pancreatitis onset occurred a median of 14 days after mesalazine initiation, with abdominal pain as the most common symptom (100%).
- Elevated serum amylase/lipase and imaging findings confirmed pancreatitis; discontinuation led to resolution in all cases, with 93.3% improving within a week. Rechallenge resulted in recurrence in 21 cases.
Conclusions:
- Mesalazine-induced AP is a rare but significant adverse drug reaction.
- The onset of AP is not dose-dependent and can occur anytime during treatment, often within two weeks.
- Discontinuation of mesalazine is effective for resolution, but the condition may recur upon rechallenge.
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