1,095 reports of this reaction
2.1% of all DEFERASIROX reports
#11 most reported adverse reaction
VOMITING is the #11 most commonly reported adverse reaction for DEFERASIROX, manufactured by Novartis Pharmaceuticals Corporation. There are 1,095 FDA adverse event reports linking DEFERASIROX to VOMITING. This represents approximately 2.1% of all 50,952 adverse event reports for this drug.
Patients taking DEFERASIROX who experience vomiting should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
VOMITING is a less commonly reported adverse event for DEFERASIROX, but still significant enough to appear in the safety profile.
In addition to vomiting, the following adverse reactions have been reported for DEFERASIROX:
The following drugs have also been linked to vomiting in FDA adverse event reports:
VOMITING has been reported as an adverse event in 1,095 FDA reports for DEFERASIROX. This does not prove causation, but indicates an association observed in post-market surveillance data.
VOMITING accounts for approximately 2.1% of all adverse event reports for DEFERASIROX, making it a notable side effect.
If you experience vomiting while taking DEFERASIROX, 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.