467 reports of this reaction
2.4% of all ADO TRASTUZUMAB EMTANSINE reports
#7 most reported adverse reaction
THROMBOCYTOPENIA is the #7 most commonly reported adverse reaction for ADO TRASTUZUMAB EMTANSINE, manufactured by Genentech, Inc.. There are 467 FDA adverse event reports linking ADO TRASTUZUMAB EMTANSINE to THROMBOCYTOPENIA. This represents approximately 2.4% of all 19,599 adverse event reports for this drug.
Patients taking ADO TRASTUZUMAB EMTANSINE 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 ADO TRASTUZUMAB EMTANSINE, but still significant enough to appear in the safety profile.
In addition to thrombocytopenia, the following adverse reactions have been reported for ADO TRASTUZUMAB EMTANSINE:
The following drugs have also been linked to thrombocytopenia in FDA adverse event reports:
THROMBOCYTOPENIA has been reported as an adverse event in 467 FDA reports for ADO TRASTUZUMAB EMTANSINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
THROMBOCYTOPENIA accounts for approximately 2.4% of all adverse event reports for ADO TRASTUZUMAB EMTANSINE, making it a notable side effect.
If you experience thrombocytopenia while taking ADO TRASTUZUMAB EMTANSINE, 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.