The most commonly reported side effects of eravacycline include off label use, blood fibrinogen decreased, and nausea, based on 207 FDA adverse event reports from 2011 to 2025. 11.6% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for eravacycline.
These are voluntary reports and do not establish that eravacycline caused these reactions.
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Other drugs that appear in adverse event reports alongside eravacycline. 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.
25.6% of eravacycline adverse event reports involve female patients and 45.9% involve male patients. The largest age group is adult at 68%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking eravacycline when the adverse event was reported.
Showing 15 of 74 indications
Eravacycline is sold under the brand name Xerava.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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