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

Free Trial Offer

KERENDIA Free Trial Offer Program Terms and Conditions

  • 1 offer valid for up to a free 30-day supply of KERENDIA® (finerenone) and must be accompanied by a valid, signed prescription for KERENDIA
  • This offer is valid only in the United States and Puerto Rico
  • Offer program shall not apply in any state or jurisdiction where prohibited
  • Prescriber ID# required on prescription
  • You should bring the offer to the pharmacy when filling the prescription
  • KERENDIA supplied free of charge through the Offer Program is not contingent on continued use of KERENDIA or any other prescriptions or use of Bayer products
  • No claim for reimbursement for product dispensed pursuant to this offer may be submitted to any patient or third party payer whether a commercial or a government payer
  • Not valid if reproduced
  • It is unlawful for any person to sell, purchase, trade, barter, or export KERENDIA supplied through the Offer Program or make an offer to do so
  • This free trial offer cannot be combined with any other rebate/offer, free trial, or similar offer for the specified prescription
  • The KERENDIA Free Trial Offer Program is not insurance and is not a discount, rebate, coupon, cost-sharing program, or other form of financial assistance and no portion of the value of the free product may count as a patient out-of-pocket expense under any health insurance program
  • You must be 18 years old or older
  • Limit 1 offer per patient; offer limited to those patients who are new to taking KERENDIA
  • Bayer reserves the right to change or discontinue this Offer Program at any time without notice

The KERENDIA Free Trial Offer may provide new patients with up to a 30-day supply of KERENDIA and must be accompanied by a valid, signed prescription for KERENDIA. This offer is valid only in the United States and Puerto Rico. Offer Program shall not apply in any state or jurisdiction where prohibited. KERENDIA supplied free of charge through the Offer Program is not contingent on continued use of KERENDIA or any other prescriptions or use of Bayer products. No claim for reimbursement for product dispensed pursuant to this offer may be submitted to any patient or third-party payer whether a commercial or a government payer. Not valid if reproduced. It is unlawful for any person to sell, purchase, trade, barter or export KERENDIA supplied through the offer program or make an offer to do so. This free-trial offer cannot be combined with any other rebate/offer, free trial or similar offer for the specified prescription. Limit 1 offer per patient. You must be 18 years old or older. Bayer reserves the right to change or discontinue this Offer Program at any time without notice.

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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.