The most commonly reported side effects of fospropofol include oedema, dermatitis allergic, and alanine aminotransferase increased, based on 14 FDA adverse event reports from 2010 to 2019.
Percentages show how often each reaction appears relative to total reports for fospropofol.
These are voluntary reports and do not establish that fospropofol caused these reactions.
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Other drugs that appear in adverse event reports alongside fospropofol. 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.
35.7% of fospropofol adverse event reports involve female patients and 64.3% involve male patients. The largest age group is adult at 45%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking fospropofol when the adverse event was reported.
Fospropofol is sold under the brand name Lusedra.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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