The most commonly reported side effects of anacaulase include inappropriate schedule of product administration, cardiac arrest, and lactic acidosis, based on 5 FDA adverse event reports from 2025 to 2025.
Percentages show how often each reaction appears relative to total reports for anacaulase.
These are voluntary reports and do not establish that anacaulase caused these reactions.
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Seriousness is determined by the reporter, not by OpenClaim.
Other drugs that appear in adverse event reports alongside anacaulase. 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
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.
40.0% of anacaulase adverse event reports involve female patients and 60.0% involve male patients. The largest age group is adult at 80%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
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