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Severe adverse reactions caused by omeprazole: A case report
Meiling Yu1, Jianghua Qian2, Daohua Guo3
1Department of Pharmacy, The First Affiliated Hospital of Bengbu Medical College, Bengbu, Anhui 233004, P.R. China; Department of Neurology, The First Affiliated Hospital of Bengbu Medical College, Bengbu, Anhui 233004, P.R. China.
Experimental and Therapeutic Medicine
|July 23, 2016
Summary
A patient experienced severe adverse reactions, including allergic shock, rash, and diarrhea, after taking omeprazole. Genetic screening revealed slow metabolism of omeprazole, leading to metabolite accumulation and these serious drug side effects.
Area of Science:
- Pharmacology
- Clinical Medicine
- Genetics
Background:
- A 61-year-old female presented with a severe whole-body rash, diarrhea, and shock.
- These symptoms emerged after a month of non-steroidal anti-inflammatory drug use for arthritis, followed by omeprazole prescription.
- Initial treatments in the ICU were ineffective, necessitating transfer to a specialized hospital.
Purpose of the Study:
- To investigate the cause of severe adverse drug reactions in a patient treated with omeprazole.
- To determine the role of genetic factors in omeprazole metabolism and subsequent toxicity.
Main Methods:
- Clinical case observation and treatment documentation.
- Genetic screening for drug-metabolizing enzymes.
- Analysis of omeprazole metabolite levels and their correlation with adverse events.
Main Results:
- The patient developed a rash, severe diarrhea, nausea, vomiting, and shock after omeprazole administration.
- Genetic analysis identified the patient as a poor metabolizer of omeprazole.
- Accumulation of omeprazole metabolites due to slow metabolism was identified as the cause of the severe adverse reactions.
Conclusions:
- Slow omeprazole metabolism in genetically predisposed individuals can lead to toxic metabolite accumulation.
- This accumulation can manifest as severe adverse reactions, including allergic shock, rash, and diarrhea.
- Genetic screening is crucial for identifying patients at risk for severe omeprazole-induced adverse events.