IVACAFTOR and DRUG DOSE OMISSION

108 reports of this reaction

1.2% of all IVACAFTOR reports

#19 most reported adverse reaction

Overview

DRUG DOSE OMISSION is the #19 most commonly reported adverse reaction for IVACAFTOR, manufactured by Vertex Pharmaceuticals Incorporated. There are 108 FDA adverse event reports linking IVACAFTOR to DRUG DOSE OMISSION. This represents approximately 1.2% of all 9,200 adverse event reports for this drug.

Patients taking IVACAFTOR who experience drug dose omission should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.

Reporting Frequency

DRUG DOSE OMISSION108 of 9,200 reports

DRUG DOSE OMISSION is a less commonly reported adverse event for IVACAFTOR, but still significant enough to appear in the safety profile.

Other Side Effects of IVACAFTOR

In addition to drug dose omission, the following adverse reactions have been reported for IVACAFTOR:

HOSPITALISATION — 1,286 reports
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS — 601 reports
PNEUMONIA — 262 reports
INFECTION — 249 reports
MALAISE — 247 reports
LOWER RESPIRATORY TRACT INFECTION — 242 reports
DEATH — 224 reports
COUGH — 219 reports
CYSTIC FIBROSIS — 211 reports
HEADACHE — 194 reports

Other Drugs Associated with DRUG DOSE OMISSION

The following drugs have also been linked to drug dose omission in FDA adverse event reports:

ACLIDINIUM BROMIDE BUDESONIDE AND FORMOTEROL FUMARATE DIHYDRATE CARBAMIDE PEROXIDE 6.5%CINACALCET HYDROCHLORIDE DALFAMPRIDINE ESOMEPRAZOLE MAGNESIUM EVOLOCUMAB FLUTICASONE PROPIONATE AND SALMETEROL INSULIN LISPRO LEDIPASVIR AND SOFOSBUVIR METHYLPHENIDATE MOMETASONE FUROATE MOMETASONE FUROATE AND FORMOTEROL FUMARATE DIHYDRATE PALIPERIDONE PALMITATE PATIROMER PEGFILGRASTIM QUETIAPINE TERIPARATIDE TETRABENAZINE UMECLIDINIUM BROMIDE AND VILANTEROL TRIFENATATE

Frequently Asked Questions

Does IVACAFTOR cause DRUG DOSE OMISSION?

DRUG DOSE OMISSION has been reported as an adverse event in 108 FDA reports for IVACAFTOR. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is DRUG DOSE OMISSION with IVACAFTOR?

DRUG DOSE OMISSION accounts for approximately 1.2% of all adverse event reports for IVACAFTOR, making it a notable side effect.

What should I do if I experience DRUG DOSE OMISSION while taking IVACAFTOR?

If you experience drug dose omission 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.

IVACAFTOR Full Profile All Drugs Causing DRUG DOSE OMISSION Vertex Pharmaceuticals Incorporated Drugs

Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.