1,530 reports of this reaction
2.4% of all DOXORUBICIN HYDROCHLORIDE reports
#8 most reported adverse reaction
ALOPECIA is the #8 most commonly reported adverse reaction for DOXORUBICIN HYDROCHLORIDE, manufactured by Baxter Healthcare Company. There are 1,530 FDA adverse event reports linking DOXORUBICIN HYDROCHLORIDE to ALOPECIA. This represents approximately 2.4% of all 64,420 adverse event reports for this drug.
Patients taking DOXORUBICIN HYDROCHLORIDE who experience alopecia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ALOPECIA is a less commonly reported adverse event for DOXORUBICIN HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to alopecia, the following adverse reactions have been reported for DOXORUBICIN HYDROCHLORIDE:
The following drugs have also been linked to alopecia in FDA adverse event reports:
ALOPECIA has been reported as an adverse event in 1,530 FDA reports for DOXORUBICIN HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ALOPECIA accounts for approximately 2.4% of all adverse event reports for DOXORUBICIN HYDROCHLORIDE, making it a notable side effect.
If you experience alopecia while taking DOXORUBICIN HYDROCHLORIDE, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.