1,286 reports of this reaction
14.0% of all IVACAFTOR reports
#1 most reported adverse reaction
HOSPITALISATION is the #1 most commonly reported adverse reaction for IVACAFTOR, manufactured by Vertex Pharmaceuticals Incorporated. There are 1,286 FDA adverse event reports linking IVACAFTOR to HOSPITALISATION. This represents approximately 14.0% of all 9,200 adverse event reports for this drug.
Patients taking IVACAFTOR who experience hospitalisation should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HOSPITALISATION is a frequently reported adverse event for IVACAFTOR, accounting for a significant proportion of all reports.
In addition to hospitalisation, the following adverse reactions have been reported for IVACAFTOR:
The following drugs have also been linked to hospitalisation in FDA adverse event reports:
HOSPITALISATION has been reported as an adverse event in 1,286 FDA reports for IVACAFTOR. This does not prove causation, but indicates an association observed in post-market surveillance data.
HOSPITALISATION accounts for approximately 14.0% of all adverse event reports for IVACAFTOR, making it one of the most commonly reported side effect.
If you experience hospitalisation while taking IVACAFTOR, 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.