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ENTRESTO is indicated in adult patients for the treatment of symptomatic chronic heart failure with reduced ejection fraction.1

Prescribe ENTRESTO® to act directly on the heart and help improve cardiac function for your chronic HFrEF patients2.

ENTRESTO has a dual mode of action that targets two complementary HF pathways, neprilysin inhibition and RAAS inhibition1.

 

 

Watch the mechanism of action video below to gain a deeper understanding of ENTRESTO’s dual blockade3

 

 

Discover how ENTRESTO can improve the heart’s structure and function, and reverse cardiac remodelling2,4,5

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Summary of the safety profile

The most commonly reported adverse events (AEs) during treatment with ENTRESTO were hypotension (17.6%), hyperkalaemia (11.6%) and renal impairment (10.1%). Angioedema was reported in patients treated with sacubitril/valsartan (0.5%).1

Common AE:
Anaemia, hypokalaemia, hypoglycaemia, dizziness, headache, syncope, vertigo, orthostatic hypotension, cough, diarrhoea, nausea, gastritis, renal failure (renal failure, acute renal failure), fatigue, asthenia.1

Very common AE:
Hyperkalaemia, hypotension, renal impairment.1

Adverse reactions are ranked by System organ class and then by frequency with the most frequent first, using the following convention: very common (≥1/10); common (≥1/100 to <1/10); uncommon (≥1/1,000 to <1/100); rare (≥1/10,000 to <1/1,000); very rare (<1/10,000).

ACEi, angiotensin-converting enzyme inhibitor; ARB, angiotensin receptor blocker; ARNI, angiotensin receptor neprilysin inhibitor; RAAS, renin-angiotensin-aldosterone system.

References:

  1. ENTRESTO Summary of Product Characteristics. Accessed May 2024 at www.medicines.ie
  2. Januzzi JL Jr, et al. JAMA 2019;322(11):1085–1095.
  3. Diez J et al. Eur J Heart Fail 2016; 19 (2) 167-176.
  4. Desai AS, et al. JAMA 2019;322(11):1077–1084.
  5. Wang Y, et al. J Am Heart Assoc 2019;8(13):e012272.
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November 2024 | IE171971-1
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Reporting of side effects
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk profile of the medicinal product. All suspected adverse reactions should be reported to HPRA Pharmacovigilance, website www.hpra.ie. Adverse events can also be reported to Novartis preferably at www.novartis.com/report, by emailing [email protected] or by calling (01) 2080 612.