6,797 reports of this reaction
3.2% of all CARBOPLATIN reports
#4 most reported adverse reaction
NAUSEA is the #4 most commonly reported adverse reaction for CARBOPLATIN, manufactured by Accord Healthcare, Inc.. There are 6,797 FDA adverse event reports linking CARBOPLATIN to NAUSEA. This represents approximately 3.2% of all 214,224 adverse event reports for this drug.
Patients taking CARBOPLATIN who experience nausea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NAUSEA is moderately reported among CARBOPLATIN users, representing a notable but not dominant share of adverse events.
In addition to nausea, the following adverse reactions have been reported for CARBOPLATIN:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 6,797 FDA reports for CARBOPLATIN. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 3.2% of all adverse event reports for CARBOPLATIN, making it a notable side effect.
If you experience nausea 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.