Loperamide: Risk of Acute Pancreatitis

User Rating: 5 / 5

Star ActiveStar ActiveStar ActiveStar ActiveStar Active
 

Overview

Loperamide is a synthetic opioid antidiarrhoeal agent. It works by decreasing the motility of the gastrointestinal tract. In Malaysia, it is indicated for the treatment of symptomatic control of acute and chronic diarrhoea. It can also be used to reduce the frequency and volume of stools and to harden their consistency in patients with an ileostomy.1

Acute pancreatitis is a transient inflammation of the pancreas associated with substantial morbidity and mortality.2-3 Gallstones and alcohol abuse are the commonest causes of acute pancreatitis, whereas drugs have been linked to approximately 2%-4.8% of reported acute pancreatitis cases.2

There are currently nine (9) loperamide-containing products registered with the Drug Control Authority (DCA), all of which are single active ingredient oral formulations.4

 

Background of the Safety Issue

The National Pharmaceutical Regulatory Agency (NPRA) has learnt from the European Medicines Agency (EMA) regarding the risk of acute pancreatitis with the use of loperamide-containing products. The EMA has considered at least a possible causal relationship between loperamide and loperamide/simeticone with acute pancreatitis, based on the available evidence from the literature, spontaneous reports including nine (9) positive de-challenges and one (1) positive re-challenge, as well as a plausible mechanism of action.5

Sphincter of Oddi dysfunction has been described as a possible mechanism for drug-induced acute pancreatitis. This sphincter controls the flow of pancreatic and biliary secretions into the small intestine. Loperamide, which has an opioid receptor affinity, may trigger the Oddi’s sphincter to produce a reflux of secretions into the pancreas, elevating pancreatic duct pressure and eventually inducing pancreatitis. Despite this hypothesis, there may also be idiosyncratic competing causes for the development of acute pancreatitis.6

According to the published literature and post-marketing reports suggestive of a plausible causal relationship, the time to onset of acute pancreatitis associated with loperamide use ranged from one (1) to five (5) days. Suspected pancreatitis with loperamide was more frequently reported in women. In certain cases, a history of cholecystectomy was also reported.6  

 

Adverse Drug Reaction Reports7

To date, the NPRA has received a total of 30 reports with 62 adverse events suspected to be caused by loperamide-containing products. The most frequently reported adverse events were related to the system organ class (SOC) of skin and subcutaneous tissue disorders, including pruritus (12 reports), rash (7), and urticaria (5). The NPRA has received no local reports of acute pancreatitis thus far; however, symptoms such as nausea (1) and vomiting (1) have been reported.

 

Advice for Healthcare Professionals

  • While NPRA is still reviewing this safety issue, be aware of the possible risk of acute pancreatitis associated with loperamide use, especially in patients with a history of cholecystectomy.
  • Advise patients taking loperamide to seek medical attention if they experience characteristic symptoms of acute pancreatitis, including epigastric abdominal pain (sometimes radiating to the back), tenderness when touching the abdomen, fever, rapid pulse, nausea, and vomiting.
  • Consider the diagnosis of acute pancreatitis in patients presenting with clinical symptoms, elevated pancreatic enzymes, and/or characteristic findings in abdominal imaging following loperamide use.
  • Early detection of acute pancreatitis and prompt withdrawal of the offending drug minimise complications and length of hospital stay.
  • Report all suspected adverse events associated with loperamide-containing products to the NPRA.

 

References:

  1. National Pharmaceutical Regulatory Agency (NPRA). IMODIUM CAPSULE 2MG (loperamide) [Package Insert]. 2021 Nov [cited 2022 Apr 4]. The Malaysian Product Registration Database (QUEST). Available from: http://www.npra.gov.my (access restricted)
  2. Chatila AT, Bilal M, Guturu P. Evaluation and management of acute pancreatitis. World J Clin Cases. 2019; 7(9): 1006-1020. Available from: https://doi.org/10.12998%2Fwjcc.v7.i9.1006
  3. Jones MR, Hall OM, Kaye AM, Kaye AD. Drug-induced acute pancreatitis: a review. Ochsner J [Internet] 2015 Spring;15(1):45-51. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4365846/
  4. National Pharmaceutical Regulatory Agency (NPRA). QUEST3+ Product Search [Internet]. 2022 [cited 2022 Apr 4] Available from: https://www.npra.gov.my 
  5. European Medicines Agency (EMA). Annex I: Scientific conclusions and grounds for the variation to the terms of the Marketing Authorisation(s) [Internet]. 2022 Mar 14 [cited 2022 May 9]. Available from: https://www.ema.europa.eu/en/documents/psusa/loperamide-loperamide/simeticone-cmdh-scientific-conclusions-grounds-variation-amendments-product-information-timetable/00010665/202105_en.pdf
  6. World Health Organization (WHO). Loperamide and acute pancreatitis in patients with a history of cholecystectomy: signal strengthening. WHO Pharmaceuticals Newsletter [Internet]. 2018 Sep [cited 2022 May 9]. Available from: https://apps.who.int/iris/bitstream/handle/10665/339949/9789240021365-eng.pdf?sequence=1&isAllowed=y  
  7. National Pharmaceutical Regulatory Agency (NPRA). The Malaysian National ADR Database (QUEST3+) [Internet]. 2022 [cited 2022 Apr 4]. Available from: https://www.npra.gov.my (access restricted)

 

DISCLAIMER

This publication is aimed at health professionals. The information is meant to provide updates on medication safety issues, and not as a substitute for clinical judgement. While reasonable care has been taken to verify the accuracy of the information at the time of publication, the NPRA shall not be held liable for any loss whatsoever arising from the use of or reliance on this publication.

 

Written by: Nafiza binti Mohd Ismail
Reviewed/Edited by: Choo Sim Mei, Lim Sze Gee, Noor'ain Shamsuddin, Dr Azuana Ramli

 

National Pharmaceutical Regulatory Agency (NPRA)
Lot 36, Jalan Universiti (Jalan Profesor Diraja Ungku Aziz), 46200 Petaling Jaya, Selangor, Malaysia.
  • Email: npra@npra.gov.my
  • Phone: +603-7883 5400
  • Fax: +603-7956 2924, +603-7956 7075

DISCLAIMER

The Government of Malaysia and the National Pharmaceutical Regulatory Agency are not responsible for any loss or damage caused by the usage of any information obtained from this website.

Mobile Web :

Site Last Modified

  • Last Modified: Tuesday 05 July 2022, 15:35:22.
© Copyright 2022 . All Rights Reserved National Pharmaceutical Regulatory Agency NPRA

Search

Main Menu English

Choose Your Language