The most commonly reported side effects of pantoprazole include chronic kidney disease, fatigue, and acute kidney injury, based on 337,160 FDA adverse event reports from 2004 to 2025. 5.6% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for pantoprazole.
These are voluntary reports and do not establish that pantoprazole caused these reactions.
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Other drugs that appear in adverse event reports alongside pantoprazole. Drugs flagged as a suspected cause appear in the first column. Drugs taken at the same time but not suspected appear in the second.
Also suspected
Taken alongside
Co-occurrence in adverse event reports does not establish a drug interaction. Patients often take multiple medications, and these lists reflect prescribing patterns rather than causal relationships. Consult a healthcare provider about potential drug interactions.
52.6% of pantoprazole adverse event reports involve female patients and 36.6% involve male patients. The largest age group is elderly at 50%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking pantoprazole when the adverse event was reported.
Showing 15 of 1,598 indications
Pantoprazole is sold under the brand name Pantoprazole Sodium In 0.9% Sodium Chloride.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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