The most commonly reported side effects of cupric sulfate include pulmonary embolism, dyspnoea, and full blood count abnormal, based on 143 FDA adverse event reports from 2006 to 2025.
Percentages show how often each reaction appears relative to total reports for cupric sulfate.
These are voluntary reports and do not establish that cupric sulfate caused these reactions.
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Other drugs that appear in adverse event reports alongside cupric sulfate. 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.
17.5% of cupric sulfate adverse event reports involve female patients and 69.2% involve male patients. The largest age group is elderly at 73%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking cupric sulfate when the adverse event was reported.
Cupric Sulfate is sold under the brand name Cupric Sulfate.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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