The Immune Deficiency Foundation (IDF) improves the diagnosis, treatment, and quality of life for every person affected by PI. The IDF fosters a community that is connected, engaged, and empowered through advocacy, education, and research.
Support
Is Available
Hypothetical patient.
Support Is Available
QIVIGY® copay program
Copay assistance is available for eligible patients on QIVIGY covered under both pharmacy and medical benefits.
Hypothetical patient.
QIVIGY® copay program
Copay assistance is available for eligible patients on QIVIGY covered under both pharmacy and medical benefits.
Eligible patients can receive up to $10,000 per calendar year to use on out-of-pocket costs for QIVIGY.
The program covers the copay, deductible, and/or co-insurance associated with the cost of QIVIGY only. The program does not cover costs associated with administration or supplies.
Copay benefit
- $10,000 per patient per year
- Electronic processing; no patient cards necessary
Program and patient eligibility guidelines
- Patients must be commercially insured
- Patients must express a financial need
- Patients' health plan permits members to participate in copay assistance programs
Program restrictions
- Not valid for prescriptions eligible for reimbursement by any federal or state healthcare programs, such as Medicare, Medicaid, Medigap, Veterans Affairs, Department of Defense, TRICARE, or any other federal or state-funded programs
QIVIGY offers comprehensive reimbursement support
A dedicated team of reimbursement specialists are ready to provide support
This support includes:
Patient-specific benefit verifications claims- Payer coverage and coding research
- Assistance with claims questions
- Appeal support for denied prior authorizations
To connect with a reimbursement specialist:
888-262-8040
reimbursementsupport@medmonk.com
Connect with patient advocacy organizations
The following list of patient advocacy groups can help support you on your journey with PI.
The Jeffrey Modell Foundation is a global nonprofit dedicated to early diagnosis, meaningful treatments and, ultimately, cures through basic and clinical research, physician and patient education, public awareness, government advocacy, patient support, newborn screening, and genetic sequencing.
The International Patient Organisation for Primary Immunodeficiencies (IPOPI) is an international nonprofit organization and the leading worldwide advocate for people with PI.
The Immunoglobulin National Society (IgNS) is a professional organization dedicated to the advancement of Ig therapy practice across clinical indications and areas of practice.
Ig, immunoglobulin; PI, primary immunodeficiency.
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