Support

The Amneal PATHways® Patient Support Program facilitates access for patients

The Amneal PATHways® Patient Support Program is designed to help patients and providers stay on course toward accessible treatment. With its full suite of services and dedicated Program Access Specialists, PATHways allows stakeholders to more easily map a patient’s personal treatment path together.


Get assistance with:
  • Benefit investigation
  • Prior authorization (PA) & reauthorization
  • Appeals
  • Billing and coding
  • Claims
Get information about:
  • Patient assistance program
  • Alternate coverage
  • Co-pay savings program

The Amneal PATHways® Patient Support Program offers comprehensive support during every phase of treatment

Enrollment includes connection to Patient Access Specialists, who will:

Explain benefits and
insurance coverage
Discuss eligibility for
affordability options
Inform about program
updates as they occur

Learn more about the Amneal PATHways® Patient Support Program.

The Amneal PATHways® Co-pay Assistance Card is available to eligible patients

Eligible,* commercially insured patients may pay as little as $0 per treatment with an Amneal Biosciences product.


  • Eligible,* commercially insured patients may pay as little as $0 per treatment with an Amneal Biosciences product
  • Limits, terms, and conditions apply
  • No income restrictions for patients to qualify
  • For information on enrollment, claims submissions, and reimbursement, log on to the PATHways provider portal at pathwaysproviderportal.com

*Eligibility Criteria/Terms & Conditions: The Amneal PATHways Co-Pay Savings Program [Program] is NOT insurance. The Program is only available for residents of the US and Puerto Rico who have commercial health insurance with co-pay/co-insurance on each prescription fill per product. Uninsured and cash-pay individuals are NOT eligible for the Program nor are individuals with commercial insurance coverage that does not provide coverage for FOCINVEZ™ (fosaprepitant injection). Individuals with coverage for FOCINVEZ™ (fosaprepitant injection), in whole or in part, under any state or federally funded healthcare program, including but not limited to, Medicare, Medicare Advantage Plans, Medicare Part D (including Qualified Retiree Prescription Drug Plans), Medicaid, Medigap, VA, DoD, TRICARE, and the Puerto Rico Government Health Insurance Plan, are NOT eligible for the Program. Patients who move from commercial to state or federally funded insurance will no longer be eligible for the Program.

Patients may not combine this offer with any rebate, coupon, free trial, or similar offer. Patients must present a valid prescription for an eligible drug at a participating pharmacy. Federal and state laws and other factors may prevent or otherwise restrict eligibility. This offer is not valid where prohibited by law. Void if copied, transferred, purchased, altered, or traded. Amneal Pharmaceuticals LLC reserves the right to rescind, revoke or amend this offer or discontinue the Program at any time without notice.

When submitting claims under the Program, patients are certifying that they understand the Program rules, regulations and terms and conditions, and will comply with the Program terms as set forth herein. Additionally, you are certifying that a claim has not been submitted under a state or federally funded healthcare program, including but not limited to, Medicare, Medicare Advantage Plans, Medicare Part D (including Qualified Retiree Prescription Drug Plans), Medicaid, Medigap, VA, DoD, TRICARE, and the Puerto Rico Government Health Insurance Plan. Limit one Program enrollment per individual.

Questions? Call 1-866-4AMNEAL (1-866-426-6325) with any questions or
concerns
Monday-Friday, 8:00 AM-8:00 PM ET.

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INDICATIONS

FOCINVEZ™ is a substance P/neurokinin-1 (NK1) receptor antagonist indicated in adults and pediatric patients 6 months of age and older, in combination with other antiemetic agents, for the prevention of:

  • acute and delayed nausea and vomiting associated with initial and repeat courses of highly emetogenic cancer chemotherapy (HEC) including high-dose cisplatin.
  • delayed nausea and vomiting associated with initial and repeat courses of moderately emetogenic cancer chemotherapy (MEC).

Limitations of Use:

FOCINVEZ™ has not been studied for the treatment of established nausea and vomiting.

IMPORTANT SAFETY INFORMATION

Contraindications

  • FOCINVEZ™ is contraindicated in patients who are hypersensitive to any component of the product.
  • Concurrent use of FOCINVEZ™ with pimozide is contraindicated.

Warnings and Precautions

  • Clinically Significant CYP3A4 Interactions: Fosaprepitant, a prodrug of aprepitant, is a weak inhibitor of CYP3A4, and aprepitant is a substrate, inhibitor, and inducer of CYP3A4.
    See full Prescribing Information for recommendations regarding contraindications, risk of adverse reactions, and dosage adjustment of FOCINVEZ™ and concomitant drugs.
  • Hypersensitivity Reactions: Serious hypersensitivity reactions, including anaphylaxis and anaphylactic shock, during or soon after infusion of fosaprepitant have occurred. Monitor patients during and after infusion. If hypersensitivity reactions occur, discontinue the infusion and administer appropriate medical therapy. Do not reinitiate FOCINVEZ™ in patients who experienced these symptoms with previous use.
  • Infusion Site Reactions: Infusion site reactions (ISRs), including thrombophlebitis and vasculitis, have been reported with the use of intravenous fosaprepitant. The majority of severe ISRs were reported with concomitant vesicant (anthracycline-based) chemotherapy administration. Avoid infusion into small veins. Discontinue infusion and administer treatment if a severe reaction develops.
  • Warfarin: Coadministration of fosaprepitant with warfarin, a CYP2C9 substrate, may result in a clinically significant decrease in the international normalized ratio (INR) of prothrombin time. Monitor the INR in patients on chronic warfarin therapy in the 2-week period, particularly at 7 to 10 days, following initiation of FOCINVEZ™ with each chemotherapy cycle.
  • Hormonal Contraceptives: The efficacy of hormonal contraceptives may be reduced during treatment with FOCINVEZ™ and for 1 month following administration of the last dose of either fosaprepitant or oral aprepitant. Advise patients to use effective alternative or back-up methods of contraception.

Adverse Drug Reactions

  • The most common adverse drug reactions in adults (≥2%) treated with FOCINVEZ™ are neutropenia, leukopenia, peripheral neuropathy, anemia, fatigue, diarrhea, asthenia, dyspepsia, urinary tract infection, pain in extremity.
  • Adverse reactions in pediatric patients treated with FOCINVEZ™ are similar to adults.

Drug Interactions

  • Co-administration of FOCINVEZ™ with drugs that are inhibitors or inducers of CYP3A4 may result in increased or decreased plasma concentrations of aprepitant.
  • See full Prescribing Information for a list of clinically significant drug interactions.

Use in Specific Populations

  • Pregnancy: There are insufficient data on the use of fosaprepitant in pregnant women to identify a drug-associated risk of major birth defects, miscarriage or other adverse maternal or fetal outcomes.
  • Lactation: There are no data on the presence of aprepitant in human milk.

To report SUSPECTED ADVERSE REACTIONS, contact Amneal Biosciences, a division of Amneal Pharmaceuticals LLC at 1-877-835-5472 or the FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

Please see accompanying full Prescribing Information.

INDICATIONS

FOCINVEZ™ is a substance P/neurokinin-1 (NK1) receptor antagonist indicated in adults and pediatric patients 6 months of age and older, in combination with other antiemetic agents, for the prevention of:

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