The most commonly reported side effects of spirapril include dyspnoea, hypotension, and fall, based on 27 FDA adverse event reports from 2006 to 2024.
Percentages show how often each reaction appears relative to total reports for spirapril.
These are voluntary reports and do not establish that spirapril caused these reactions.
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Other drugs that appear in adverse event reports alongside spirapril. 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.
48.1% of spirapril adverse event reports involve female patients and 48.1% involve male patients. The largest age group is elderly at 56%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking spirapril when the adverse event was reported.
Spirapril is sold under the brand name Renormax.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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