1,460 reports of this reaction
12.1% of all LUMACAFTOR AND IVACAFTOR reports
#1 most reported adverse reaction
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS is the #1 most commonly reported adverse reaction for LUMACAFTOR AND IVACAFTOR, manufactured by Vertex Pharmaceuticals Incorporated. There are 1,460 FDA adverse event reports linking LUMACAFTOR AND IVACAFTOR to INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS. This represents approximately 12.1% of all 12,020 adverse event reports for this drug.
Patients taking LUMACAFTOR AND IVACAFTOR who experience infective pulmonary exacerbation of cystic fibrosis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS is a frequently reported adverse event for LUMACAFTOR AND IVACAFTOR, accounting for a significant proportion of all reports.
In addition to infective pulmonary exacerbation of cystic fibrosis, the following adverse reactions have been reported for LUMACAFTOR AND IVACAFTOR:
The following drugs have also been linked to infective pulmonary exacerbation of cystic fibrosis in FDA adverse event reports:
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS has been reported as an adverse event in 1,460 FDA reports for LUMACAFTOR AND IVACAFTOR. This does not prove causation, but indicates an association observed in post-market surveillance data.
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS accounts for approximately 12.1% of all adverse event reports for LUMACAFTOR AND IVACAFTOR, making it one of the most commonly reported side effect.
If you experience infective pulmonary exacerbation of cystic fibrosis 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.