The most commonly reported side effects of amodiaquine include stillbirth, abortion, and death, based on 36 FDA adverse event reports from 2005 to 2025.
Percentages show how often each reaction appears relative to total reports for amodiaquine.
These are voluntary reports and do not establish that amodiaquine caused these reactions.
Report severity
Seriousness is determined by the reporter, not by OpenClaim.
Other drugs that appear in adverse event reports alongside amodiaquine. 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.
36.1% of amodiaquine adverse event reports involve female patients and 13.9% 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 amodiaquine when the adverse event was reported.
Amodiaquine is sold under the brand name Camoquin Hydrochloride.
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.