NOW APPROVED for adults with heart failure with an ejection fraction of 40% or more

NOW APPROVED for adults with heart failure with an ejection fraction of 40% or more

KERENDIA Savings Card Terms & Conditions

  • Patient must meet the eligibility requirements of the KERENDIA Savings Card; for example, only commercially insured patients are eligible
  • Patient must inform the KERENDIA Savings Card of change in insurance status
  • It is required that the patient understand, accept, and meet the terms of all the KERENDIA Savings Card requirements
  • Use of the KERENDIA Savings Card must be consistent with and not prohibited by the requirements of the patient’s health insurance
  • Benefit limitations apply
  • The KERENDIA Savings Card is for commercially insured patients using KERENDIA for an approved FDA indication
  • The KERENDIA Savings Card does not cover costs for charges associated with patient visits
  • Offer valid only for patients treated in the USA, including Puerto Rico, Guam and US Territories
  • Bayer reserves the right to determine eligibility, monitor participation, equitably distribute product and modify or discontinue the KERENDIA Savings Card at any time with or without notice
  • Patient agrees to provide necessary health information to the administrators of the KERENDIA Savings Card
  • You must be 18 years old or older

For questions about the KERENDIA Savings Program, please call us at 888-KERENDIA (537-3634).

Patients are eligible if they are commercially insured and may pay as little as $0 per month. Benefit limitations apply. Patients who are enrolled in any type of government insurance or reimbursement programs are not eligible. As a condition precedent of the copayment support provided under this program, e.g., copay refunds, participating patients and pharmacies are obligated to inform insurance companies and third-party payers of any benefits they receive and the value of this program, and may not participate if this program is prohibited by or conflicts with their private insurance policy, as required by contract or otherwise. Void where prohibited by law, taxed, or restricted. Patients enrolled in the Bayer US Patient Assistance Foundation are not eligible. Bayer may determine eligibility, monitor participation, equitably distribute product and modify or discontinue any aspect of the KERENDIA $0 Copay Program at any time, including but not limited to this commercial copay assistance program.

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What is KERENDIA?

KERENDIA (finerenone) is a prescription medicine used to:

  • reduce the risk of worsening of kidney disease, kidney failure, death due to cardiovascular disease, heart attack, and hospitalization for heart failure in adults with chronic kidney disease (CKD) associated with type 2 diabetes (T2D) (10mg, 20mg tablets)
  • reduce the risk of death due to cardiovascular disease, hospitalization for heart failure, and urgent heart failure visits in adults with heart failure with left ventricular ejection fraction (HF LVEF) of ≥40%, when the heart may pump normally, but may not fill properly (10mg, 20mg, 40mg tablets)

Important Safety Information

Do not take KERENDIA if you:
  • Are allergic to any of the ingredients in KERENDIA
  • Take certain medications called CYP3A4 inhibitors. Ask your healthcare provider if you are not sure if you are taking any of these medications
  • Have problems with your adrenal glands
What are the possible side effects of KERENDIA?

KERENDIA may cause serious side effects, including:

  • High potassium levels in your blood (hyperkalemia). Your healthcare provider will check your potassium level before and during treatment with KERENDIA
  • Worsening of kidney function for patients with heart failure. Your healthcare provider will measure your kidney function before and during treatment with KERENDIA

The most common side effects of KERENDIA include hyperkalemia (potassium level in your blood that is higher than normal), hypotension (blood pressure that is lower than normal), and hyponatremia (sodium level in your blood that is lower than normal). Worsening of kidney function was also included in patients with heart failure.

Before you take KERENDIA, tell your healthcare provider about all your medical conditions, including if you:
  • Have high potassium levels in your blood (hyperkalemia) or take medications that may increase potassium levels in your blood
  • Have severe liver problems
  • Are pregnant or plan to become pregnant, or are breastfeeding or plan to breastfeed. Avoid breastfeeding during treatment with KERENDIA and 1 day after treatment
Tell your healthcare provider about all the prescription and over-the-counter medicines you take, including salt substitutes, vitamins, and herbal or potassium supplements.
  • KERENDIA may affect the way other medications work, and other medications may affect how KERENDIA works. Do not start or stop any medicine before you talk with your healthcare provider. Avoid grapefruit or grapefruit juice as it may increase KERENDIA levels in the blood

Please see the full Prescribing Information for KERENDIA.

Important Safety Information

Do not take KERENDIA if you:
  • Are allergic to any of the ingredients in KERENDIA
  • Take certain medications called CYP3A4 inhibitors. Ask your healthcare provider if you are not sure if you are taking any of these medications
  • Have problems with your adrenal glands
What are the possible side effects of KERENDIA?

KERENDIA may cause serious side effects, including:

  • High potassium levels in your blood (hyperkalemia). Your healthcare provider will check your potassium level before and during treatment with KERENDIA
  • Worsening of kidney function for patients with heart failure. Your healthcare provider will measure your kidney function before and during treatment with KERENDIA

The most common side effects of KERENDIA include hyperkalemia (high potassium level in your blood), hyperkalemia (potassium level in your blood that is higher than normal), hypotension (blood pressure that is lower than normal), and hyponatremia (sodium level in your blood that is lower than normal). Worsening of kidney function was also included in patients with heart failure.

Before you take KERENDIA, tell your healthcare provider about all your medical conditions, including if you:
  • Have high potassium levels in your blood (hyperkalemia) or take medications that may increase potassium levels in your blood
  • Have severe liver problems
  • Are pregnant or plan to become pregnant, or are breastfeeding or plan to breastfeed. Avoid breastfeeding during treatment with KERENDIA and 1 day after treatment
Tell your healthcare provider about all the prescription and over-the-counter medicines you take, including salt substitutes, vitamins, and herbal or potassium supplements.
  • KERENDIA may affect the way other medications work, and other medications may affect how KERENDIA works. Do not start or stop any medicine before you talk with your healthcare provider. Avoid grapefruit or grapefruit juice as it may increase KERENDIA levels in the blood

Please see the full Prescribing Information for KERENDIA.