The most commonly reported side effects of ceruletide include sepsis, wound dehiscence, and syncope, based on 2 FDA adverse event reports from 2007 to 2012.
Percentages show how often each reaction appears relative to total reports for ceruletide.
These are voluntary reports and do not establish that ceruletide caused these reactions.
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Other drugs that appear in adverse event reports alongside ceruletide. 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.
100.0% of ceruletide adverse event reports involve female patients and 0.0% involve male patients. The largest age group is adult at 100%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Ceruletide is sold under the brand name Tymtran.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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