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vutrisiran injection

vutrisiran injection
for subcutaneous use Initial U.S. Approval: 2022

AMVUTTRA is a prescription medicine that treats the polyneuropathy caused by an illness called hereditary transthyretin‑mediated amyloidosis (hATTR amyloidosis). AMVUTTRA is used in adults only.

Facts about vutrisiran injection

Approval Date: 6/13/2022
Proprietary Name: Amvuttra
Active Ingredient(s): vutrisiran
FDA-approved use: To treat polyneuropathy of hereditary transthyretin-mediated amyloidosis
Dosage Form: Injection: 25 mg/0.5 mL in a single-dose prefilled syringe
Summary of FDA-approved use on approval date: Click Here
(see Drugs@FDA for complete indication)

Access the best support services globally

If you have a prescription from a Registered Medical Practitioner (RMP), IPN in Delhi can assist you in obtaining access to genuine medication.  Our professional will provide you with a step-by-step guide on how to legally and safely import “vutrisiran injection” based on the information you provide.

Indian Pharma Network (IPN) Legitimate consultant and facilitator in the New Delhi, India. IPN has over two decades of industry experience and extensive coverage throughout India, including major cities such as Mumbai, Kolkata, Hyderabad, Chennai, Ahmedabad, Delhi, Bangalore, Srinagar, Jammu, Jaipur, Chandigarh, Ludhiana, Noida, Gurgaon, Lucknow, the North East, Pune, and other regions.

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Query For vutrisiran injection

Approved accessible "vutrisiran injection"

Amvuttra (vutrisiran) injection to treat polyneuropathy (damage of multiple nerves throughout the body) in adults with hereditary transthyretin-mediated amyloidosis, a disease that leads to organ and tissue dysfunction.

Vutrisiran, sold under the brand name Amvuttra, is a medication used for the treatment of the polyneuropathy of hereditary transthyretin-mediated (hATTR) amyloidosis in adults. It is a small interfering RNA (siRNA) that interferes with the expression of the transthyretin (TTR) gene. vutrisiran is indicated for the treatment of the polyneuropathy of hereditary transthyretin-mediated amyloidosis in adults. Note: (see Drugs@FDA for complete indication) Vutrisiran was approved for medical use in the United States in June 2022, and in the European Union in September 2022.

How can 1 go about obtaining vutrisiran injection?

If vutrisiran injection are not yet approved or available in your area, you may request its price in India under a specific brand name through IPN. For assistance and guidance, you can contact us by providing complete details. Our pharmaceutical expert will help you find a suitable and practical solution to your query. To receive comprehensive support, please call us at +91 9891 296 838 (Mr. Tarun) / +91 9811 747 774 (Mr. Neeraj).

Amvuttra (vutrisiran) injection for subcutaneous use Initial U.S. Approval: 2022

Indian Pharma Network (IPN), New Delhi. India

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