6,305 reports of this reaction
2.9% of all CARBOPLATIN reports
#5 most reported adverse reaction
FEBRILE NEUTROPENIA is the #5 most commonly reported adverse reaction for CARBOPLATIN, manufactured by Accord Healthcare, Inc.. There are 6,305 FDA adverse event reports linking CARBOPLATIN to FEBRILE NEUTROPENIA. This represents approximately 2.9% of all 214,224 adverse event reports for this drug.
Patients taking CARBOPLATIN who experience febrile neutropenia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
FEBRILE NEUTROPENIA is a less commonly reported adverse event for CARBOPLATIN, but still significant enough to appear in the safety profile.
In addition to febrile neutropenia, the following adverse reactions have been reported for CARBOPLATIN:
The following drugs have also been linked to febrile neutropenia in FDA adverse event reports:
FEBRILE NEUTROPENIA has been reported as an adverse event in 6,305 FDA reports for CARBOPLATIN. This does not prove causation, but indicates an association observed in post-market surveillance data.
FEBRILE NEUTROPENIA accounts for approximately 2.9% of all adverse event reports for CARBOPLATIN, making it a notable side effect.
If you experience febrile neutropenia while taking CARBOPLATIN, 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.