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Simplified access. Coordinated care. ProCeed Customer Solutions Intake Forms and Quick Reference Guide PROVIDE SOLUTIONS TO Streamline access to VIEKIRA PAK for your patients using the enclosed proCeed.

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How to fill out the ProCeed Patient Assistance Program - VIEKIRA PAK online

The ProCeed Patient Assistance Program - VIEKIRA PAK provides a streamlined approach to access treatment for hepatitis C for eligible patients. This guide offers clear, step-by-step instructions to assist users in accurately completing the online form, ensuring a seamless application process.

Follow the steps to accurately complete the form online.

  1. Click ‘Get Form’ button to obtain the form and open it in your editor.
  2. In the 'Requested Services' section, select all applicable boxes for the services you are requesting, such as Prescription/Benefit Verification or Patient Assistance Program (PAP) Review.
  3. Fill out the 'Patient Information' section with the patient's name, date of birth, gender, contact information, and insurance details. Ensure to include the last four digits of the social security number.
  4. Complete the 'Prescriber Information' section, providing details about the prescribing physician, including their name, contact information, and specialty.
  5. In the 'Diagnosis and Clinical Information' section, indicate the HCV genotype, treatment history, and provide details about insurance coverage.
  6. Proceed to the 'Prescription Information' section where you will check the appropriate box for medication, specify dosage, and list directions, quantity, and refills.
  7. Sign and date the form to certify that the information is accurate. Remember, stamps are not allowed for signatures.
  8. Review all sections for completeness and accuracy. Once confirmed, save your changes, then download, print, or share the form as needed.

Complete your ProCeed Patient Assistance Program application online today to ensure timely access to your treatment.

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Dasabuvir is a Hepatitis C Virus Non-Nucleoside NS5B Palm Polymerase Inhibitor. The mechanism of action of dasabuvir is as a RNA Replicase Inhibitor, and UGT1A1 Inhibitor, and Breast Cancer Resistance Protein Inhibitor.

Ombitasvir, dasabuvir, and paritaprevir were FDA approved in July 2016 for the treatment of hepatitis C (Table 5.1). Ombitasvir is a direct-acting antiviral medication used as part of combination therapy to treat chronic hepatitis C, an infectious liver disease caused by infection with the hepatitis C virus (HCV).

Manufacturer for United States The Viekira Pak (vee-KEE-rah-pak) contains the fixed-dose combination of ombitasvir-paritaprevir- plus dasabuvir) (Figure 1) and (Figure 2). It is manufactured by AbbVie.

VIEKIRA PAK is the only FDA-approved regimen that contains three distinct mechanisms of action - NS5A inhibitor, NS3/4A protease inhibitor and a non-nucleoside NS5B polymerase inhibitor - that work together to attack the virus at three separate stages of the disease lifecycle to inhibit it from reproducing.

Official answer. Viekira Pak contains two separate tablets co-packaged, and Viekira XR is a single fixed-dose combination tablet. Viekira Pak and Viekira XR both contain the same four ingredient drugs for the treatment of adult patients with chronic hepatitis C virus (HCV) genotype 1 infection.

The mechanism of action of paritaprevir is as a HCV NS3/4A Protease Inhibitor, and Organic Anion Transporting Polypeptide 1B1 Inhibitor, and Organic Anion Transporting Polypeptide 1B3 Inhibitor, and Breast Cancer Resistance Protein Inhibitor, and UGT1A1 Inhibitor, and P-Glycoprotein Inhibitor.

VIEKIRA PAK with or without is indicated for the treatment of patients with genotype 1 chronic hepatitis C virus (HCV) infection including those with compensated cirrhosis.

The Viekira Pak is an all-oral regimen comprised of four medications: ombitasvir, paritaprevir, , and dasabuvir. This regimen can be used with or without . In the Viekira Pak, the ombitasvir-paritaprevir- are combined as a fixed-dose tablet and the dasabuvir is a separate tablet.

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