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How to Complete the
ONPATTRO (Parisian)
Start Formulas see Important Safety Information on page 7
and accompanying full Prescribing Information. How to complete the ONPATTRO (Parisian)
Start Form
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How to fill out onpattro patisiran annotated start
How to fill out onpattro patisiran annotated start
01
Check the prescription to ensure that Onpattro (patisiran) is the correct medication to be administered.
02
Review the patient's medical history and any relevant laboratory results.
03
Prepare the Onpattro (patisiran) solution according to the manufacturer's instructions.
04
Administer the medication via intravenous infusion as directed by the healthcare provider.
05
Monitor the patient for any adverse reactions during and after the infusion.
06
Document the administration of Onpattro (patisiran) in the patient's medical records.
Who needs onpattro patisiran annotated start?
01
Patients with hereditary transthyretin amyloidosis (hATTR) who have been prescribed Onpattro (patisiran) by their healthcare provider.
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What is onpattro patisiran annotated start?
Onpattro (patisiran) is a medication used to treat hereditary transthyretin amyloidosis. The annotated start refers to the official process and documentation required for its use.
Who is required to file onpattro patisiran annotated start?
Healthcare providers and facilities that administer Onpattro are required to file the annotated start.
How to fill out onpattro patisiran annotated start?
To fill out the annotated start, providers must complete the specific forms detailing patient information, dosage, administration details, and any other required clinical data.
What is the purpose of onpattro patisiran annotated start?
The purpose is to ensure proper documentation and compliance for the administration of Onpattro, facilitating monitoring and reporting of treatment outcomes.
What information must be reported on onpattro patisiran annotated start?
Information required includes patient demographics, diagnosis, dosage details, administration route, treatment duration, and any adverse effects observed.
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