Omaveloxolone: Difference between revisions
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|indication=Friedreich's ataxia in adults and adolescents aged 16 years and older. | |indication=Friedreich's ataxia in adults and adolescents aged 16 years and older. | ||
|adverseReactions=transamnitis, headache, nausea, abdominal pain, fatigue, diarrhea, and musculoskeletal pain | |adverseReactions=transamnitis, headache, nausea, abdominal pain, fatigue, diarrhea, and musculoskeletal pain | ||
|fdaLIADAdult=omaveloxolone (SKYCLARYS) is used for the treatment of friedreich ataxia for adults and adolescents of age above 16 years. | |||
The recommended dosage is 150mg (3 tablets of 50mg) taken orally once daily. | |||
|contraindications=none | |||
|warnings=Elevation of AST/ALT- | |||
In the clinical study it showed incidence of elevations of ALT or AST above 5 times and 3 times the upper limit of normal (ULN) was 16% and 31%, respectively, in patients treated with SKYCLARYS. Monitor ALT, AST, and total bilirubin prior to initiation of SKYCLARYS, every month for the first 3 months of treatment, and periodically thereafter. Discontinue SKYCLARYS and repeat liver function tests as soon as possible, if there is transaminases increase to levels greater than 5 times the ULN, or greater than 3 times the ULN with evidence of liver dysfunction (e.g., elevated bilirubin). | |||
Elevation of B-Type Natriuretic Peptide- | |||
Treatment with SKYCLARYS can cause elevation in BNP. Cardiomyopathy and cardiac failure are common in patients with Friedreich's ataxia. | |||
Patient should be monitored for signs and symptoms of fluid overload like sudden weight gain (3 pounds or more of weight gain in one day, or 5 pounds or more of weight gain in a week), peripheral edema, palpitations, and shortness of breath. | |||
Abnormalities in the lipid profile- | |||
}} | }} |
Revision as of 23:02, 1 May 2024
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Alen Antony Pathil, M.D.[2]
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Overview
Omaveloxolone is a Nuclear factor -like 2 (Nrf2) pathway activator that is FDA approved for the treatment of Friedreich's ataxia in adults and adolescents aged 16 years and older.. Common adverse reactions include transamnitis, headache, nausea, abdominal pain, fatigue, diarrhea, and musculoskeletal pain.
Adult Indications and Dosage
FDA-Labeled Indications and Dosage (Adult)
omaveloxolone (SKYCLARYS) is used for the treatment of friedreich ataxia for adults and adolescents of age above 16 years.
The recommended dosage is 150mg (3 tablets of 50mg) taken orally once daily.
Off-Label Use and Dosage (Adult)
Pediatric Indications and Dosage
FDA-Labeled Indications and Dosage (Pediatric)
There is limited information regarding Omaveloxolone FDA-Labeled Indications and Dosage (Pediatric) in the drug label.
Off-Label Use and Dosage (Pediatric)
Contraindications
none
Warnings
Elevation of AST/ALT- In the clinical study it showed incidence of elevations of ALT or AST above 5 times and 3 times the upper limit of normal (ULN) was 16% and 31%, respectively, in patients treated with SKYCLARYS. Monitor ALT, AST, and total bilirubin prior to initiation of SKYCLARYS, every month for the first 3 months of treatment, and periodically thereafter. Discontinue SKYCLARYS and repeat liver function tests as soon as possible, if there is transaminases increase to levels greater than 5 times the ULN, or greater than 3 times the ULN with evidence of liver dysfunction (e.g., elevated bilirubin).
Elevation of B-Type Natriuretic Peptide- Treatment with SKYCLARYS can cause elevation in BNP. Cardiomyopathy and cardiac failure are common in patients with Friedreich's ataxia. Patient should be monitored for signs and symptoms of fluid overload like sudden weight gain (3 pounds or more of weight gain in one day, or 5 pounds or more of weight gain in a week), peripheral edema, palpitations, and shortness of breath.
Abnormalities in the lipid profile-
Adverse Reactions
Clinical Trials Experience
There is limited information regarding Omaveloxolone Clinical Trials Experience in the drug label.
Postmarketing Experience
There is limited information regarding Omaveloxolone Postmarketing Experience in the drug label.
Drug Interactions
There is limited information regarding Omaveloxolone Drug Interactions in the drug label.
Use in Specific Populations
Pregnancy
Pregnancy Category (FDA):
There is no FDA guidance on usage of Omaveloxolone in women who are pregnant.
Pregnancy Category (AUS):
There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Omaveloxolone in women who are pregnant.
Labor and Delivery
There is no FDA guidance on use of Omaveloxolone during labor and delivery.
Nursing Mothers
There is no FDA guidance on the use of Omaveloxolone in women who are nursing.
Pediatric Use
There is no FDA guidance on the use of Omaveloxolone in pediatric settings.
Geriatic Use
There is no FDA guidance on the use of Omaveloxolone in geriatric settings.
Gender
There is no FDA guidance on the use of Omaveloxolone with respect to specific gender populations.
Race
There is no FDA guidance on the use of Omaveloxolone with respect to specific racial populations.
Renal Impairment
There is no FDA guidance on the use of Omaveloxolone in patients with renal impairment.
Hepatic Impairment
There is no FDA guidance on the use of Omaveloxolone in patients with hepatic impairment.
Females of Reproductive Potential and Males
There is no FDA guidance on the use of Omaveloxolone in women of reproductive potentials and males.
Immunocompromised Patients
There is no FDA guidance one the use of Omaveloxolone in patients who are immunocompromised.
Administration and Monitoring
Administration
There is limited information regarding Omaveloxolone Administration in the drug label.
Monitoring
There is limited information regarding Omaveloxolone Monitoring in the drug label.
IV Compatibility
There is limited information regarding the compatibility of Omaveloxolone and IV administrations.
Overdosage
There is limited information regarding Omaveloxolone 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 Omaveloxolone Pharmacology in the drug label.
Mechanism of Action
There is limited information regarding Omaveloxolone Mechanism of Action in the drug label.
Structure
There is limited information regarding Omaveloxolone Structure in the drug label.
Pharmacodynamics
There is limited information regarding Omaveloxolone Pharmacodynamics in the drug label.
Pharmacokinetics
There is limited information regarding Omaveloxolone Pharmacokinetics in the drug label.
Nonclinical Toxicology
There is limited information regarding Omaveloxolone Nonclinical Toxicology in the drug label.
Clinical Studies
There is limited information regarding Omaveloxolone Clinical Studies in the drug label.
How Supplied
There is limited information regarding Omaveloxolone How Supplied in the drug label.
Storage
There is limited information regarding Omaveloxolone Storage in the drug label.
Images
Drug Images
{{#ask: Page Name::Omaveloxolone |?Pill Name |?Drug Name |?Pill Ingred |?Pill Imprint |?Pill Dosage |?Pill Color |?Pill Shape |?Pill Size (mm) |?Pill Scoring |?NDC |?Drug Author |format=template |template=DrugPageImages |mainlabel=- |sort=Pill Name }}
Package and Label Display Panel
{{#ask: Label Page::Omaveloxolone |?Label Name |format=template |template=DrugLabelImages |mainlabel=- |sort=Label Page }}
Patient Counseling Information
There is limited information regarding Omaveloxolone Patient Counseling Information in the drug label.
Precautions with Alcohol
Alcohol-Omaveloxolone interaction has not been established. Talk to your doctor regarding the effects of taking alcohol with this medication.
Brand Names
There is limited information regarding Omaveloxolone Brand Names in the drug label.
Look-Alike Drug Names
There is limited information regarding Omaveloxolone 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.