Anifrolumab-fnia
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Tejasvi Aryaputra
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Overview
Anifrolumab-fnia is a type I interferon receptor antagonist that is FDA approved for the treatment of moderate-to severe systemic lupus erythematousus along with standard therapy. Common adverse reactions include bronchitis, nasopharyngitis, herpes zoster, upper respiratory tract infections, infusion related reactions, and cough.
Adult Indications and Dosage
FDA-Labeled Indications and Dosage (Adult)
There is limited information regarding Anifrolumab-fnia FDA-Labeled Indications and Dosage (Adult) in the drug label.
Off-Label Use and Dosage (Adult)
Guideline-Supported Use
There is limited information regarding Off-Label Guideline-Supported Use of Anifrolumab-fnia in adult patients.
Non–Guideline-Supported Use
There is limited information regarding Off-Label Non–Guideline-Supported Use of Anifrolumab-fnia in adult patients.
Pediatric Indications and Dosage
FDA-Labeled Indications and Dosage (Pediatric)
There is limited information regarding Anifrolumab-fnia FDA-Labeled Indications and Dosage (Pediatric) in the drug label.
Off-Label Use and Dosage (Pediatric)
Guideline-Supported Use
There is limited information regarding Off-Label Guideline-Supported Use of Anifrolumab-fnia in pediatric patients.
Non–Guideline-Supported Use
There is limited information regarding Off-Label Non–Guideline-Supported Use of Anifrolumab-fnia in pediatric patients.
Contraindications
There is limited information regarding Anifrolumab-fnia Contraindications in the drug label.
Warnings
There is limited information regarding Anifrolumab-fnia Warnings' in the drug label.
Adverse Reactions
Clinical Trials Experience
There is limited information regarding Anifrolumab-fnia Clinical Trials Experience in the drug label.
Postmarketing Experience
There is limited information regarding Anifrolumab-fnia Postmarketing Experience in the drug label.
Drug Interactions
There is limited information regarding Anifrolumab-fnia Drug Interactions in the drug label.
Use in Specific Populations
Pregnancy
Pregnancy Category (FDA):
There is no FDA guidance on usage of Anifrolumab-fnia in women who are pregnant.
Pregnancy Category (AUS):
There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Anifrolumab-fnia in women who are pregnant.
Labor and Delivery
There is no FDA guidance on use of Anifrolumab-fnia during labor and delivery.
Nursing Mothers
There is no FDA guidance on the use of Anifrolumab-fnia in women who are nursing.
Pediatric Use
There is no FDA guidance on the use of Anifrolumab-fnia in pediatric settings.
Geriatic Use
There is no FDA guidance on the use of Anifrolumab-fnia in geriatric settings.
Gender
There is no FDA guidance on the use of Anifrolumab-fnia with respect to specific gender populations.
Race
There is no FDA guidance on the use of Anifrolumab-fnia with respect to specific racial populations.
Renal Impairment
There is no FDA guidance on the use of Anifrolumab-fnia in patients with renal impairment.
Hepatic Impairment
There is no FDA guidance on the use of Anifrolumab-fnia in patients with hepatic impairment.
Females of Reproductive Potential and Males
There is no FDA guidance on the use of Anifrolumab-fnia in women of reproductive potentials and males.
Immunocompromised Patients
There is no FDA guidance one the use of Anifrolumab-fnia in patients who are immunocompromised.
Administration and Monitoring
Administration
There is limited information regarding Anifrolumab-fnia Administration in the drug label.
Monitoring
There is limited information regarding Anifrolumab-fnia Monitoring in the drug label.
IV Compatibility
There is limited information regarding the compatibility of Anifrolumab-fnia and IV administrations.
Overdosage
There is limited information regarding Anifrolumab-fnia overdosage. If you suspect drug poisoning or overdose, please contact the National Poison Help hotline (1-800-222-1222) immediately.
Pharmacology
There is limited information regarding Anifrolumab-fnia Pharmacology in the drug label.
Mechanism of Action
There is limited information regarding Anifrolumab-fnia Mechanism of Action in the drug label.
Structure
There is limited information regarding Anifrolumab-fnia Structure in the drug label.
Pharmacodynamics
There is limited information regarding Anifrolumab-fnia Pharmacodynamics in the drug label.
Pharmacokinetics
There is limited information regarding Anifrolumab-fnia Pharmacokinetics in the drug label.
Nonclinical Toxicology
There is limited information regarding Anifrolumab-fnia Nonclinical Toxicology in the drug label.
Clinical Studies
There is limited information regarding Anifrolumab-fnia Clinical Studies in the drug label.
How Supplied
There is limited information regarding Anifrolumab-fnia How Supplied in the drug label.
Storage
There is limited information regarding Anifrolumab-fnia Storage in the drug label.
Images
Drug Images
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Package and Label Display Panel
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Patient Counseling Information
There is limited information regarding Anifrolumab-fnia Patient Counseling Information in the drug label.
Precautions with Alcohol
Alcohol-Anifrolumab-fnia interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.
Brand Names
There is limited information regarding Anifrolumab-fnia Brand Names in the drug label.
Look-Alike Drug Names
There is limited information regarding Anifrolumab-fnia Look-Alike Drug Names in the drug label.
Drug Shortage Status
Price
References
The contents of this FDA label are provided by the National Library of Medicine.