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Provide patients with support throughout their treatment with KERENDIA

And for those eligible patients, utilize the following to help patients access KERENDIA:

Kerendia Savings Card stating eligible patients may pay as little as $0 per month

$0 Patient Savings Card for Commercial Patients

Eligible patients may pay as little as $0 per month for KERENDIA.*

To activate the KERENDIA Savings Card:

Call 1-888-537-3634 or Text SAVE to 53736, or visit

Once activated, patients may show the card to their pharmacist and the offer will be applied to the prescription.

Kerendia voucher program with a free trial offer

30-day Free Trial Voucher

New patients can start on KERENDIA at no cost by using the KERENDIA Free Trial Voucher.

New patients are eligible for the (30-day) Free Trial Voucher regardless of insurance.

To get or activate a KERENDIA Free Trial Voucher:

Call 1-888-537-3634 or
Text VOUCHER to 53736 or

Simply bring the KERENDIA Free Trial Voucher to the pharmacy—we’ll do the rest.

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Patients who need help paying for their KERENDIA prescription should call 1-888-KERENDIA (537-3634) or visit to learn more about the affordability options offered by Bayer.


If you cannot afford your prescription medication, Bayer may be able to help.

The Bayer US Patient Assistance Foundation is a charitable organization that helps eligible patients get their Bayer prescription medicine at no cost. Please have your patient contact the program at 1-866-2BUSPAF (228-7723) Monday–Friday, 9:00 AM–6:00 PM EST, or visit the foundation website at to see if they might qualify for assistance.

*Patients are eligible if they are commercially insured and may pay as little as $0 and save up to $3000 per year. Patients who are enrolled in any type of government insurance or reimbursement programs are not eligible. Full terms and conditions apply. See

By texting SAVE to 53736 to enroll or activate the card, you agree to receive recurring automated KERENDIA Savings Program messages, which may include savings alerts, refill reminders, and other messages related to your participation in the program. Consent to receiving SMS messages is not a condition of purchase of goods or services. Message and data rates may apply. Message frequency varies. Text STOP to opt out. Text HELP for help. Terms & Conditions and Privacy Policy apply. For T&C, click here. For Privacy Policy, click here. For SMS Terms, click here.

Terms and Conditions apply. Call 888-KERENDIA or visit for more information.

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KERENDIA is indicated to reduce the risk of sustained eGFR decline, end-stage kidney disease, cardiovascular death, non-fatal myocardial infarction, and hospitalization for heart failure in adult patients with chronic kidney disease (CKD) associated with type 2 diabetes (T2D)



  • Concomitant use with strong CYP3A4 inhibitors
  • Patients with adrenal insufficiency


  • Hyperkalemia: KERENDIA can cause hyperkalemia. The risk for developing hyperkalemia increases with decreasing kidney function and is greater in patients with higher baseline potassium levels or other risk factors for hyperkalemia. Measure serum potassium and eGFR in all patients before initiation of treatment with KERENDIA and dose accordingly. Do not initiate KERENDIA if serum potassium is >5.0 mEq/L


    Measure serum potassium periodically during treatment with KERENDIA and adjust dose accordingly. More frequent monitoring may be necessary for patients at risk for hyperkalemia, including those on concomitant medications that impair potassium excretion or increase serum potassium


  • From the pooled data of 2 placebo-controlled studies, the adverse reactions reported in ≥1% of patients on KERENDIA and more frequently than placebo were hyperkalemia (14% vs 6.9%), hypotension (4.6% vs 3.9%), and hyponatremia (1.3% vs 0.7%)


  • Strong CYP3A4 Inhibitors: Concomitant use of KERENDIA with strong CYP3A4 inhibitors is contraindicated. Avoid concomitant intake of grapefruit or grapefruit juice
  • Moderate and Weak CYP3A4 Inhibitors: Monitor serum potassium during drug initiation or dosage adjustment of either KERENDIA or the moderate or weak CYP3A4 inhibitor and adjust KERENDIA dosage as appropriate
  • Strong and Moderate CYP3A4 Inducers: Avoid concomitant use of KERENDIA with strong or moderate CYP3A4 inducers


  • Lactation: Avoid breastfeeding during treatment with KERENDIA and for 1 day after treatment
  • Hepatic Impairment: Avoid use of KERENDIA in patients with severe hepatic impairment (Child Pugh C) and consider additional serum potassium monitoring with moderate hepatic impairment (Child Pugh B)

Please read the Prescribing Information for KERENDIA.