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HomeAboutDMDMTrial design and efficacySafety and tolerabilityDosing and infusion ratesPatient profilescITPcITPTrial design and efficacySafety and tolerabilityDosing and infusion ratesMaterialsSupportSupportOCTAGAM 10% Co-Pay ProgramPfizer IGuide™FAQsRequest a RepresentativeIg CompanionCoverage
Prescribing Information, including BOXED WARNINGIndicationsPatient SiteOCTAGAM 5%
Coverage
Find OCTAGAM 10% coverage information in your area†
Cost and coverage calculator

†Some plans may not display due to health plan-specific policy.
The information provided is not a guarantee of coverage of payment (partial or full) and is subject to change without notice.

Access and enrollment based on MMIT formulary information as of [EFFECTIVE_DATE] and represents the local area, based on the first three digits of the ZIP code.
Access based on MMIT formulary information as of [EFFECTIVE_DATE].

ST = Step Therapy. Coverage may require Prior Authorization.

†Formulary data provided by Managed Markets Insight & Technology, LLC, (MMIT) are updated monthly and current as of [EFFECTIVE_DATE]. The information provided is not a guarantee of coverage or payment (partial or full) and is subject to change without notice. Please confirm coverage with each patient’s plan. Formulary status does not imply safety or efficacy of any product.

‡The OCTAGAM Co-Pay Program provides eligible patients assistance of up to $12,500 per year. Once a patient reaches the annual maximum benefit, patient is responsible for paying the remaining monthly out-of-pocket costs. The OCTAGAM Co-Pay Program is good only in the US and Puerto Rico. No membership fees. Federal and state health care beneficiaries are not eligible. Private insurance only. Eligibility and restrictions apply. See full Terms and Conditions on the Support and financial assistance page.

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Cost and coverage calculator

*Some plans may not display due to health plan–specific policy.

The information provided is not a guarantee of coverage of payment (partial or full) and is subject to change without notice.

Patients in your area have access to EUCRISA without restriction or after a trial of one plan-designated topical corticosteroid†

Access and enrollment based on MMIT formulary information as of [EFFECTIVE_DATE] and represents the local area, based on the first three digits of the ZIP code.
Access based on MMIT formulary information as of [EFFECTIVE_DATE].

UR – Unrestricted, PA – Prior Authorization, SE – Step Edit/Step Therapy

*Access is defined as no formulary restrictions or trial of one plan-designated topical corticosteroid (TCS).

Not a guarantee of coverage and subject to change. Patients can learn more about their coverage by contacting eucrisa•4•you, their employer, health plan, pharmacy benefits manager(PBM), or retail pharmacy.

†This information relates solely to the formulary status of Eucrisa and is not intended to imply that these products have comparable clincial efficacy or safety profiles or that these products are interchangable. These agents may not have comparable FDA-approved indications.

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May not be a comprehensive list of plans.

Data on file. Pfizer Inc., New York, NY.

†Additional plan limitations may apply relevant to a look back period of time or duration of TCS use.

OCTAGAM 10% Co-Pay Program

With the OCTAGAM Co-Pay Program, eligible patients may pay as little as $0‡

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INDICATIONS AND USAGE OCTAGAM® 10% [Immune Globulin Intravenous (Human)] liquid is indicated for the treatment of chronic immune thrombocytopenic purpura (cITP) to rapidly raise platelet counts to control or prevent bleeding in adults and for dermatomyositis (DM) in adults.
 Please click here for full Prescribing Information, including BOXED WARNING.
IMPORTANT SAFETY INFORMATION WARNING: THROMBOSIS, RENAL DYSFUNCTION, AND ACUTE RENAL FAILURE
  • Thrombosis may occur with immune globulin intravenous (IgIV) products, including OCTAGAM 10% liquid. Risk factors may include: advanced age, prolonged immobilization, hypercoagulable conditions, history of venous or arterial thrombosis, use of estrogens, indwelling central vascular catheters, hyperviscosity, and cardiovascular risk factors. Thrombosis may occur in the absence of known risk factors.
  • Renal dysfunction, acute renal failure, osmotic nephrosis, and death may occur in predisposed patients who receive IgIV products, including OCTAGAM 10% liquid. Patients predisposed to renal dysfunction include those with a degree of pre-existing renal insufficiency, diabetes mellitus, age greater than 65, volume depletion, sepsis, paraproteinemia, or patients receiving known nephrotoxic drugs. Renal dysfunction and acute renal failure occur more commonly in patients receiving IgIV products containing sucrose. OCTAGAM 10% liquid does not contain sucrose.
  • For patients at risk of thrombosis, renal dysfunction, or acute renal failure, administer OCTAGAM 10% liquid at the minimum dose and infusion rate practicable. Ensure adequate hydration in patients before administration. Monitor for signs and symptoms of thrombosis and assess blood viscosity in patients at risk for hyperviscosity.
Dosing and Administration Patients with dermatomyositis are at increased risk for thromboembolic events; monitor carefully and do not exceed an infusion rate of 0.04 mL/kg/min. ContraindicationsOCTAGAM 10% liquid is contraindicated in patients who have a history of severe systemic hypersensitivity reactions, such as anaphylaxis, to human immunoglobulin and in IgA-deficient patients with antibodies against IgA and history of hypersensitivity.Warnings and PrecautionsOCTAGAM 10% liquid may cause hypersensitivity in patients with a corn allergy. OCTAGAM 10% liquid contains maltose, which is derived from corn. Monitor renal function, including blood urea nitrogen and serum creatinine, and urine output in patients at risk of developing acute renal failure. Falsely elevated blood glucose readings may occur during and after the infusion of OCTAGAM 10% liquid with testing by some glucometers and test strip systems. Hyperproteinemia, increased serum osmolarity, and hyponatremia may occur in patients receiving OCTAGAM 10% liquid. Hemolysis that is either intravascular or due to enhanced red blood cell sequestration can develop subsequent to treatment with OCTAGAM 10% liquid. Risk factors for hemolysis include high doses and non–O-blood group. Closely monitor patients for hemolysis and hemolytic anemia. Aseptic meningitis syndrome may occur in patients receiving OCTAGAM 10% liquid, especially with high doses or rapid infusion. Monitor patients for pulmonary adverse reactions (transfusion-related acute lung injury [TRALI]). OCTAGAM 10% liquid is made from human plasma and may contain infectious agents, eg, viruses and, theoretically, the Creutzfeldt-Jakob disease agent. Adverse Reactions cITP - The most common adverse reactions reported in >5% of study subjects were headache, fever, and increased heart rate. DM - The most common adverse reactions reported in >5% of study subjects were headache, fever, nausea, vomiting, increased blood pressure, chills, musculoskeletal pain, increased heart rate, dyspnea, and infusion site reactions.You are encouraged to report adverse events related to Pfizer products by calling 1-800-438-1985 (US only). If you prefer, you may contact the US Food and Drug Administration (FDA) directly.
Visit www.fda.gov/MedWatch or call 1-800-FDA-1088.OCTAGAM® is a registered trademark of Octapharma AG.Please click here for full Prescribing Information, including BOXED WARNING.INDICATIONS AND USAGEOCTAGAM® 10% [Immune Globulin Intravenous (Human)] liquid is indicated for the treatment of chronic immune thrombocytopenic purpura (cITP) to rapidly raise platelet counts to control or prevent bleeding in adults and for dermatomyositis (DM) in adults.