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Empagliflozin
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Empagliflozin
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Empagliflozin
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Empagliflozin

Empagliflozin

The same Boehringer Ingelheim medicine previously supplied as Jardiance® (empagliflozin)

See what’s changed
Empagliflozin banner

Empagliflozin can offer
TRIPLE PROTECTION for eligible patients vs placebo1-3

T2D, CKD, and/or CVD are interrelated and progressive conditions that can lead to multisystem dysfunction4-6

Explore clinical support
NICE guidance thumbnail

Empagliflozin is simple to initiate at 10 mg dosing across all indications in adults.

Empagliflozin - Dosing and administration

Time icon
Once daily dosing, any time of day
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Swallow whole with water, with or without food
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No upper age limit*

Empagliflozin is not recommended in severe hepatic impairment, should not be used in breastfeeding or type 1 diabetes, and is contraindicated in patients with hypersensitivity to the active ingredient or any of its excipients. Empagliflozin should be avoided in pregnancy. Always refer to the SmPC before prescribing.

*Caution should be exercised in patients for whom an Empagliflozin-induced drop in blood pressure could pose a risk, such as patients with known cardiovascular disease, patients on anti-hypertensive therapy with a history of hypotension or patients aged 75 years and older.

Dose recommendations based on eGFR (mL/min/1.732)

Empagliflozin dosing table

Safety information

Concise summaries of key clinical evidence

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Type 2 diabetes

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Chronic kidney disease

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Chronic heart failure

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CRM Hub

Initiatives and tools that support earlier identification and informed action across cardio-renal-metabolic disease.

Explore the Map
CKD interactive map

“I want to understand the potential number of people  living with CKD in my population.”

Explore the Map
Protect the Kidney
Protect the kidney

“I want to slow CKD progression and reduce cardiovascular risk.”

Protect the Kidney
Act Early
Act Early

“I want to protect my patients with cardiorenal risk before it’s too late.”

Act Early

Featured Resource

Celebrating a decade of evidence: EMPA-REG OUTCOME® (2015–2025)

Explore the landmark cardiovascular outcomes trial and its continued relevance to the understanding of cardio-renal-metabolic risk. Access evidence, insights and educational resources that support clinical discussions today.

Explore now
EMPA-REG OUTCOME® (2015–2025)

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Abbreviations

CHF: chronic heart failure; CKD: chronic kidney failure; CVD: cardiovascular disease; HF: heart failure; NICE: National Institute for Health and Care Excellence; SGLT2i: sodium-glucose co-transporter-2 inhibitor; T2D: type 2 diabetes mellitus.

  1. Zinman B, et al. N Engl J Med. 2015;373(22):2117–2128.
  2. Haring HU, et al. Diabetes Care. 2014;37:1650–1659.
  3. Herrington WG, et al. N Engl J Med. 2023;388(2):117–127. (EMPA-KIDNEY results and the publication’s Supplementary Appendix.)
  4. Heidenreich PA, Bozkurt B, Aguilar D, et al. 2022 AHA/ACC/HFSA Guideline for the Management of Heart Failure: a report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines. J Am Coll Cardiol. 2022;79(17):e263-e421.
  5. Kadowaki T, Maegawa H, Watada H, Yabe D, Node K, Murohara T, Wada J. Diabetes Obes Metab. 2022;24(12):2283-2296.
  6. de Boer IH, Khunti K, Sadusky T, et al. Diabetes Care. 2022;45(12):3075-3090.
  7. National Institute for Health and Care Excellence (NICE) 2023. Empagliflozin for treating chronic heart failure with preserved or mildly reduced ejection fraction. Technology Appraisal Guidance TA929. Available from: https://www.nice.org.uk/guidance/ta929.
  8. National Institute for Health and Care Excellence (NICE) 2015. Empagliflozin in combination therapy for treating type 2 diabetes. Technology Appraisal Guidance TA336. Available from: https://www.nice.org.uk/guidance/ta336.
  9. National Institute for Health and Care Excellence (NICE) 2023. Empagliflozin for treating chronic kidney disease. Technology Appraisal Guidance TA942. Available from: https://www.nice.org.uk/guidance/ta942.
  10. National Institute for Health and Care Excellence (NICE) 2022. Empagliflozin for treating chronic heart failure with reduced ejection fraction TA773. Available at: https://www.nice.org.uk/guidance/ta773.
  11. Empagliflozin Summary of Product Characteristics (SmPC).

PC-GB-112291 | April 2026

Reporting adverse events

Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard. Adverse events should also be reported to Boehringer Ingelheim Drug Safety on 0800 328 1627 (freephone).

Please be aware that this website contains promotional information about Boehringer Ingelheim medicines and services. Some of this may not be directly relevant to your scope of practice and it is your own decision whether you choose to view this information.

Disclaimer

The content on this website is in relation to adult patients.

Empagliflozin is not recommended in severe hepatic impairment, breastfeeding, Type 1 diabetes and is contraindicated in patients with hypersensitivity to the active ingredient or any of its excipients. Empagliflozin should be avoided in pregnancy.

Please consult the SmPC for full details regarding adverse events, monitoring requirements and interactions prior to prescribing Empagliflozin.

  1. Empagliflozin UK Summary of Product Characteristics (SmPC).
Indications

Empagliflozin is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise

  • as monotherapy when metformin is considered inappropriate due to intolerance
  • in addition to other medicinal products for the treatment of diabetes1

Empagliflozin is indicated in adults for the treatment of chronic kidney disease.1

Empagliflozin is indicated in adults for the treatment of symptomatic chronic heart failure.1

PC-GB-112290 | April 2026

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