Monoferric provides multifaceted support and solutions

Pharmacosmos Therapeutics is committed to providing a seamless access journey to patients and healthcare providers and offers support to help you address any IDA treatment needs. To help you ensure your patients receive Monoferric the way you intended, we have assembled a collection of resources and tools.

Coverage, access, and hub support
  • Benefits verification
  • Claims and appeals assistance
  • Sample letters of appeal and/or medical necessity
  • Prior authorization assistance
  • Financial assistance
  • In-person support for providers’ offices by providing access to a local field reimbursement manager
  • Buy-and-bill information
Billing, coding, and reimbursement information
  • Billing and coding guide
  • Sample annotated claim forms
  • Sample letters of appeal and medical necessity
On-demand field support
  • Support to assist with your patient reimbursement needs
  • Patient benefits verification
  • Case follow-up
Patient assistance program for eligible patients
  • Available for eligible uninsured or underinsured patients (patients with claims covered, paid or reimbursed, in whole or in part, by Medicaid, Medicare, or other federal or state healthcare programs are not eligible for this program)
Copay assistance program for eligible patients
  • Available for patient with commercial health insurance
Help navigating step therapy
  • Assistance navigating step therapy and help with legislative hurdles including Step Therapy Exception Requests

Hear Dr Bahrain explain the benefits of the Monoferric Patient Solutions® Program

The The Monoferric Patient Solutions® Program has been helpful to those who have trouble accessing intravenous iron. The program is well coordinated and supportive to the patients and their needs.

There is also the availability of Nurse Educators for infusion staff.

3 ways to enroll your patients in the program
  1. Log into the HCP Portal
  2. Call us at 1-800-992-9022
Monday to Friday, from 8 AM to 
8 PM ET (except holidays)
  3. Download and fax enrollment form
The Monoferric Patient Solutions Patient Assistance Program for underinsured/uninsured patients Download the Monoferric Patient Solutions Copay Assistance Program Flashcard

Your Monoferric support team

Locate a Field Reimbursement Manager in your area or connect with a Sales Rep.

This information is general in nature and for informational purposes only. In no way should this information be considered a guarantee of coverage or reimbursement for any product or service. Coding and coverage policies change periodically, often without warning. The responsibility to determine coverage and reimbursement parameters and appropriate coding for a particular patient or procedure is always the responsibility of the provider.

Terms and Conditions:

  • Prescribed Monoferric for an on-label diagnosis
  • This offer is valid for commercially insured patients only
  • All information applicable to the MPS Copay Assistance Program requested on the enrollment form must be provided and all certifications must be signed. Forms that are modified or do not contain all the necessary information will not be eligible for benefits under the MPS Copay Assistance Program
  • Depending on insurance coverage, eligible patients receive savings of up to $2000 for Monoferric, up to a maximum savings limit of $4000 annually. Patients must have out-of-pocket costs of over $0 to participate. Patient out-of-pocket expenses for Monoferric may vary
  • This offer is not valid for patients enrolled in Medicare, Medicare Advantage, Medicaid, TRICARE, Veteran Affairs healthcare, a state prescription drug assistance program, the Government Health Insurance Plan available in Puerto Rico (formerly known as “La Reforma de Salud”) or any other federal or state healthcare programs
  • Patients may not use the MPS Copay Assistance Program if the entire cost of the patient’s Monoferric prescription is reimbursable by their commercial insurance plan or other commercial health or pharmacy benefit programs
  • The MPS Copay Assistance Program is valid for the patient’s out-of-pocket cost for Monoferric only. It is not valid for any other out-of-pocket costs (for example, office visit charges or medication administration charges) even if such costs are associated with the administration of Monoferric. Claim for Monoferric must be submitted by provider to patient’s private health insurance separately from other services and products
  • The patient’s healthcare professional must submit an explanation of benefits (EOB) statement from the patient’s commercial insurance provider within 120 days of the date of service for the patient to receive assistance under the MPS Copay Assistance Program. No EOB may be submitted more than 90 days after the expiration or [termination date of the program], and the EOB must be for administration of Monoferric prior to the program expiration or termination date. The EOB must reflect the patient’s out-of-pocket cost for Monoferric and submission of the claim by the patient’s physician for the cost of the medication
  • Patient enrollment is for the calendar year and each patient may reenroll in the MPS Copay Assistance Program in subsequent years, as needed
  • The patient should not participate in the program if his/her insurer or health plan prohibits use of manufacturer coupons/copay assistance
  • Patients must be 18 years of age or older to participate in the MPS Copay Assistance Program
  • Offer good only in the USA, including Puerto Rico, at participating pharmacies or healthcare providers
  • This patient savings under the MPS Copay Assistance Program may not be combined with any other coupon, discount, prescription savings card, free trial, or other offer
  • Void if prohibited by law, taxed, or restricted
  • The funds provided for a specific patient case are not transferable. The selling, purchasing, trading, or counterfeiting of a patient’s unique account number is strictly prohibited
  • This program is not health insurance
  • This offer is not conditioned on any past or future purchases
  • Data related to your receipt of financial assistance under the MPS Copay Assistance Program may be collected, analyzed, and shared with Pharmacosmos, for market research and other purposes related to assessing Pharmacosmos’s programs. Data shared with Pharmacosmos will be aggregated and deidentified; it will be combined with data related to other program use and will not identify you
  • Pharmacosmos Therapeutics Inc. reserves the right to rescind, revoke, or amend this offer without notice
  • By redeeming this assistance, you acknowledge that you are an eligible patient and that you understand and agree to comply with the terms and conditions of this offer
  • Qualified patients receiving Monoferric will be allowed a 120-day retroactive enrollment period to receive benefits under the program rules

IDA=iron deficiency anemia.

IMPORTANT SAFETY INFORMATION

Monoferric is contraindicated in patients with a history of serious hypersensitivity to Monoferric or any of its components. Reactions have included shock, clinically significant hypotension, loss of consciousness, and/or collapse.

INDICATIONS

Monoferric is indicated for the treatment of iron deficiency anemia (IDA) in adult patients:

  • who have intolerance to oral iron or have had unsatisfactory response to oral iron
  • who have non-hemodialysis dependent chronic kidney disease (NDD-CKD)

IMPORTANT SAFETY INFORMATION

CONTRAINDICATIONS

Monoferric is contraindicated in patients with a history of serious hypersensitivity to Monoferric or any of its components. Reactions have included shock, clinically significant hypotension, loss of consciousness, and/or collapse.

WARNINGS AND PRECAUTIONS

Hypersensitivity Reactions

Serious hypersensitivity reactions, including anaphylactic-type reactions, some of which have been life-threatening and fatal, have been reported in patients receiving Monoferric. Patients may present with shock, clinically significant hypotension, loss of consciousness, and/or collapse. Monitor patients for signs and symptoms of hypersensitivity during and after Monoferric administration for at least 30 minutes and until clinically stable following completion of the infusion. Only administer Monoferric when personnel and therapies are immediately available for the treatment of serious hypersensitivity reactions. Monoferric is contraindicated in patients with prior serious hypersensitivity reactions to Monoferric or any of its components. In clinical trials in patients with IDA and CKD, serious or severe hypersensitivity were reported in 0.3% (6/2008) of the Monoferric treated subjects. These included 3 events of hypersensitivity in 3 patients; 2 events of infusion-related reactions in 2 patients and 1 event of asthma in one patient.

Iron Overload

Excessive therapy with parenteral iron can lead to excess iron storage and possibly iatrogenic hemosiderosis or hemochromatosis. Monitor the hematologic response (hemoglobin and hematocrit) and iron parameters (serum ferritin and transferrin saturation) during parenteral iron therapy. Do not administer Monoferric to patients with iron overload.

ADVERSE REACTIONS

Adverse reactions were reported in 8.6% (172/2008) of patients treated with Monoferric. Adverse reactions related to treatment and reported by ≥1% of the treated patients were nausea (1.2%) and rash (1%). Adjudicated serious or severe hypersensitivity reactions were reported in 6/2008 (0.3%) patients in the Monoferric group. Hypophosphatemia (serum phosphate <2.0 mg/dL) was reported in 3.5% of Monoferric-treated patients in Trials 1 & 2.

To report adverse events, please contact Pharmacosmos at 1-888-828-0655. You may also contact the FDA at www.fda.gov/medwatch or 1-800-FDA-1088.

Please see Full Prescribing Information.