3,884 reports of this reaction
3.1% of all ETOPOSIDE reports
#6 most reported adverse reaction
THROMBOCYTOPENIA is the #6 most commonly reported adverse reaction for ETOPOSIDE, manufactured by Accord Healthcare Inc.. There are 3,884 FDA adverse event reports linking ETOPOSIDE to THROMBOCYTOPENIA. This represents approximately 3.1% of all 126,466 adverse event reports for this drug.
Patients taking ETOPOSIDE 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 moderately reported among ETOPOSIDE users, representing a notable but not dominant share of adverse events.
In addition to thrombocytopenia, the following adverse reactions have been reported for ETOPOSIDE:
The following drugs have also been linked to thrombocytopenia in FDA adverse event reports:
THROMBOCYTOPENIA has been reported as an adverse event in 3,884 FDA reports for ETOPOSIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
THROMBOCYTOPENIA accounts for approximately 3.1% of all adverse event reports for ETOPOSIDE, making it a notable side effect.
If you experience thrombocytopenia while taking ETOPOSIDE, 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.