The most commonly reported side effects of piperacetazine include dyspnoea, face oedema, and urticaria, based on 67 FDA adverse event reports from 2005 to 2025.
Percentages show how often each reaction appears relative to total reports for piperacetazine.
These are voluntary reports and do not establish that piperacetazine caused these reactions.
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Other drugs that appear in adverse event reports alongside piperacetazine. 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.
46.3% of piperacetazine adverse event reports involve female patients and 47.8% involve male patients. The largest age group is elderly at 64%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking piperacetazine when the adverse event was reported.
Piperacetazine is sold under the brand name Quide.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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