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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does IVACAFTOR Cause Intentional dose omission? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Intentional dose omission have been filed in association with IVACAFTOR (Kalydeco). This represents 0.1% of all adverse event reports for IVACAFTOR.

5
Reports of Intentional dose omission with IVACAFTOR
0.1%
of all IVACAFTOR reports
0
Deaths
3
Hospitalizations

How Dangerous Is Intentional dose omission From IVACAFTOR?

Of the 5 reports, 3 (60.0%) required hospitalization.

Is Intentional dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for IVACAFTOR. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does IVACAFTOR Cause?

Hospitalisation (1,209) Infective pulmonary exacerbation of cystic fibrosis (550) Infection (227) Malaise (226) Lower respiratory tract infection (224) Pneumonia (215) Death (203) Cough (180) Cystic fibrosis (167) Headache (163)

What Other Drugs Cause Intentional dose omission?

DUPILUMAB (2,269) CERTOLIZUMAB PEGOL (1,253) ADALIMUMAB (845) TOFACITINIB (845) INFLIXIMAB (815) ABALOPARATIDE (623) ETANERCEPT (615) AMBRISENTAN (595) SODIUM OXYBATE (580) CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)

Which IVACAFTOR Alternatives Have Lower Intentional dose omission Risk?

IVACAFTOR vs IVACAFTOR\LUMACAFTOR IVACAFTOR vs IVACAFTOR\TEZACAFTOR IVACAFTOR vs IVERMECTIN IVACAFTOR vs IVOSIDENIB IVACAFTOR vs IXABEPILONE

Related Pages

IVACAFTOR Full Profile All Intentional dose omission Reports All Drugs Causing Intentional dose omission IVACAFTOR Demographics