The most commonly reported side effects of desirudin include anaemia, gastrointestinal disorder, and haematemesis, based on 6 FDA adverse event reports from 2005 to 2020.
Percentages show how often each reaction appears relative to total reports for desirudin.
These are voluntary reports and do not establish that desirudin caused these reactions.
Report severity
Seriousness is determined by the reporter, not by OpenClaim.
Other drugs that appear in adverse event reports alongside desirudin. 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.
83.3% of desirudin adverse event reports involve female patients and 16.7% involve male patients. The largest age group is adult at 50%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking desirudin when the adverse event was reported.
Desirudin is sold under the brand name Iprivask.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
Ask OpenClaim about your specific drug combination. Get a sourced report using FDA data, drug labels, and medical literature.