354 reports of this reaction
1.7% of all BENDAMUSTINE HYDROCHLORIDE reports
#18 most reported adverse reaction
THROMBOCYTOPENIA is the #18 most commonly reported adverse reaction for BENDAMUSTINE HYDROCHLORIDE, manufactured by Cephalon, LLC. There are 354 FDA adverse event reports linking BENDAMUSTINE HYDROCHLORIDE to THROMBOCYTOPENIA. This represents approximately 1.7% of all 20,231 adverse event reports for this drug.
Patients taking BENDAMUSTINE HYDROCHLORIDE who experience thrombocytopenia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
THROMBOCYTOPENIA is a less commonly reported adverse event for BENDAMUSTINE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to thrombocytopenia, the following adverse reactions have been reported for BENDAMUSTINE HYDROCHLORIDE:
The following drugs have also been linked to thrombocytopenia in FDA adverse event reports:
THROMBOCYTOPENIA has been reported as an adverse event in 354 FDA reports for BENDAMUSTINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
THROMBOCYTOPENIA accounts for approximately 1.7% of all adverse event reports for BENDAMUSTINE HYDROCHLORIDE, making it a notable side effect.
If you experience thrombocytopenia while taking BENDAMUSTINE 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.