162 reports of this reaction
1.3% of all LUMACAFTOR AND IVACAFTOR reports
#18 most reported adverse reaction
CYSTIC FIBROSIS RESPIRATORY INFECTION SUPPRESSION is the #18 most commonly reported adverse reaction for LUMACAFTOR AND IVACAFTOR, manufactured by Vertex Pharmaceuticals Incorporated. There are 162 FDA adverse event reports linking LUMACAFTOR AND IVACAFTOR to CYSTIC FIBROSIS RESPIRATORY INFECTION SUPPRESSION. This represents approximately 1.3% of all 12,020 adverse event reports for this drug.
Patients taking LUMACAFTOR AND IVACAFTOR who experience cystic fibrosis respiratory infection suppression should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
CYSTIC FIBROSIS RESPIRATORY INFECTION SUPPRESSION is a less commonly reported adverse event for LUMACAFTOR AND IVACAFTOR, but still significant enough to appear in the safety profile.
In addition to cystic fibrosis respiratory infection suppression, the following adverse reactions have been reported for LUMACAFTOR AND IVACAFTOR:
The following drugs have also been linked to cystic fibrosis respiratory infection suppression in FDA adverse event reports:
CYSTIC FIBROSIS RESPIRATORY INFECTION SUPPRESSION has been reported as an adverse event in 162 FDA reports for LUMACAFTOR AND IVACAFTOR. This does not prove causation, but indicates an association observed in post-market surveillance data.
CYSTIC FIBROSIS RESPIRATORY INFECTION SUPPRESSION accounts for approximately 1.3% of all adverse event reports for LUMACAFTOR AND IVACAFTOR, making it a notable side effect.
If you experience cystic fibrosis respiratory infection suppression while taking LUMACAFTOR AND 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.