296 reports of this reaction
2.7% of all EPIRUBICIN HYDROCHLORIDE reports
#8 most reported adverse reaction
ASTHENIA is the #8 most commonly reported adverse reaction for EPIRUBICIN HYDROCHLORIDE, manufactured by Pharmacia & Upjohn Company LLC. There are 296 FDA adverse event reports linking EPIRUBICIN HYDROCHLORIDE to ASTHENIA. This represents approximately 2.7% of all 10,973 adverse event reports for this drug.
Patients taking EPIRUBICIN HYDROCHLORIDE who experience asthenia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ASTHENIA is a less commonly reported adverse event for EPIRUBICIN HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to asthenia, the following adverse reactions have been reported for EPIRUBICIN HYDROCHLORIDE:
The following drugs have also been linked to asthenia in FDA adverse event reports:
ASTHENIA has been reported as an adverse event in 296 FDA reports for EPIRUBICIN HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ASTHENIA accounts for approximately 2.7% of all adverse event reports for EPIRUBICIN HYDROCHLORIDE, making it a notable side effect.
If you experience asthenia while taking EPIRUBICIN 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.