Vutrisiran Dosage
Medically reviewed by Drugs.com. Last updated on Feb 13, 2025.
Applies to the following strengths: 25 mg/0.5 mL
Usual Adult Dose for:
Additional dosage information:
Usual Adult Dose for Hereditary Amyloidosis
Recommended dose: 25 mg administered by subcutaneous injection once every 3 months
Use: Treatment of the polyneuropathy of hereditary transthyretin-mediated amyloidosis in adults.
Renal Dose Adjustments
Mild and Moderate Renal Dysfunction: No adjustment recommended.
Severe Renal Dysfunction and End-Stage Renal Disease: Data not available
Liver Dose Adjustments
Mild Liver Dysfunction: No adjustment recommended.
Moderate and Severe Liver Dysfunction: Data not available
Precautions
US FDA requires a medication guide to assure safe use. For additional information: www.fda.gov/drugs/drug-safety-and-availability/medication-guides
CONTRAINDICATIONS: None
Safety and efficacy have not been established in patients younger than 18 years.
To report suspected adverse reactions, contact the FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
Consult WARNINGS section for additional precautions.
Dialysis
Data not available
Other Comments
Administration advice:
- This drug is for subcutaneous administration only.
- Should be administered by a healthcare professional.
- Read the US FDA-approved patient labeling for further preparation and administration instructions.
- Vitamin A supplementation is recommended.
Storage requirements:
- Store at 2C to 30C (36F to 86F) in the original carton until ready for use.
- Do not freeze.
Monitoring:
- Vitamin A serum levels prior and during treatment
Patient advice:
- Read the Patient Information and Instructions for Use.
- Female patients should inform their healthcare provider if they are pregnant or planning to become pregnant while taking this drug.
- Patients should contact their healthcare provider if they experience ocular symptoms suggestive of vitamin A deficiency such as night blindness.
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- Drug class: miscellaneous metabolic agents
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