Alnylam Assist® Can Support Your Patients

Alnylam Assist® provides personalized support for patients throughout treatment with ONPATTRO® (patisiran).

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Call me: 1-833-256-2748

Monday - Friday, 8am - 6pm ET

How Alnylam Assist® Can Help

Alnylam Assist® offers a wide range of services to guide your patients through treatment with ONPATTRO® (patisiran).

Alnylam Assist® - Understanding Your Benefits

Benefit Verification

Help determining
patient-specific coverage

Alnylam Assist® - Financial Assistance Options

Financial Assistance

Information about patients'
eligibility for financial assistance

Alnylam Assist® - Disease and Treatment Education

Patient Education

Disease and product education
for patients and families

Alnylam Assist® Reimbursement Support Icon

Reimbursement Support

Education about the prior authorization,
claims, and appeals processes


Forms and Documents

Download the materials below for more information about Alnylam Assist®.

Alnylam Assist® Services Overview Brochure (PDF)

Alnylam Assist® Services Overview Brochure for HCPs thumbnail



Alnylam Assist® Brochure (PDF)

Alnylam Assist® Brochure for Patients thumbnail


Alnylam Assist® Case Managers

Enroll Your Patients

Call an Alnylam Assist® Case Manager IconCall: 1-833-256-2748 Monday - Friday, 8am - 6pm ET

Begin the conversation with our team and help your patients join Alnylam Assist® today.

Alnylam Assist® - Support Team

Take Action Now

Together with your patient (in office)

Important Safety Information

Infusion-Related Reactions

Infusion-related reactions (IRRs) have been observed in patients treated with ONPATTRO® (patisiran). In a controlled clinical study, 19% of ONPATTRO-treated patients experienced IRRs, compared to 9% of placebo-treated patients. The most common symptoms of IRRs with ONPATTRO were flushing, back pain, nausea, abdominal pain, dyspnea, and headache.

To reduce the risk of IRRs, patients should receive premedication with a corticosteroid, acetaminophen, and antihistamines (H1 and H2 blockers) at least 60 minutes prior to ONPATTRO infusion. Monitor patients during the infusion for signs and symptoms of IRRs. If an IRR occurs, consider slowing or interrupting the infusion and instituting medical management as clinically indicated. If the infusion is interrupted, consider resuming at a slower infusion rate only if symptoms have resolved. In the case of a serious or life-threatening IRR, the infusion should be discontinued and not resumed. 

Reduced Serum Vitamin A Levels and Recommended Supplementation

ONPATTRO treatment leads to a decrease in serum vitamin A levels. Supplementation at the recommended daily allowance (RDA) of vitamin A is advised for patients taking ONPATTRO. Higher doses than the RDA should not be given to try to achieve normal serum vitamin A levels during treatment with ONPATTRO, as serum levels do not reflect the total vitamin A in the body.

Patients should be referred to an ophthalmologist if they develop ocular symptoms suggestive of vitamin A deficiency (e.g. night blindness).

Adverse Reactions

The most common adverse reactions that occurred in patients treated with ONPATTRO were upper respiratory tract infections (29%) and infusion-related reactions (19%).


ONPATTRO is indicated for the treatment of the polyneuropathy of hereditary transthyretin-mediated amyloidosis in adults.

For additional information about ONPATTRO, please see the full Prescribing Information.