The most commonly reported side effects of potassium aminosalicylate include general physical health deterioration, dyspnoea, and anaemia, based on 456 FDA adverse event reports from 2004 to 2025.
Percentages show how often each reaction appears relative to total reports for potassium aminosalicylate.
These are voluntary reports and do not establish that potassium aminosalicylate caused these reactions.
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Other drugs that appear in adverse event reports alongside potassium aminosalicylate. 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.
55.3% of potassium aminosalicylate adverse event reports involve female patients and 41.4% involve male patients. The largest age group is elderly at 65%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking potassium aminosalicylate when the adverse event was reported.
Showing 15 of 23 indications
Potassium Aminosalicylate is sold under the brand name Paskalium.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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