Ramipril
Brand names: Tritace, Altace
Ramipril is an orally active ACE inhibitor used for hypertension, heart failure, after myocardial infarction, and to reduce cardiovascular risk in patients with established vascular disease or diabetes with end-organ involvement.
ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.
Clinical monograph
How it works
It is a prodrug converted to ramiprilat, which inhibits angiotensin-converting enzyme, reducing angiotensin II formation and aldosterone secretion to cause vasodilatation and to lower blood pressure, with additional reduction of bradykinin breakdown.
Prescribing in practice
- Avoid in pregnancy and stop promptly if a patient becomes pregnant — ACE inhibitors are foetotoxic, causing oligohydramnios and renal and skull defects; it is also contraindicated with a history of angioedema.
- Do not combine with aliskiren or another renin-angiotensin blocker, and use cautiously alongside potassium-sparing diuretics, potassium supplements or NSAIDs because of hyperkalaemia and renal impairment risk.
- Initiate at a low dose with the first dose at bedtime where volume-depleted or on diuretics, as first-dose hypotension can occur, particularly in heart failure and bilateral renal artery stenosis.
Monitoring
Check renal function and serum potassium before starting, shortly after initiation and after each dose increase, and monitor blood pressure throughout.
Counselling the patient
- A dry persistent cough is common; report it as the drug may need changing.
- Seek urgent help for swelling of the face, lips or tongue or difficulty breathing.
- Rise slowly from sitting or lying to limit dizziness.
Evidence & guidelines
Cardiovascular and renal benefits are supported by large outcome trials and endorsed in NICE hypertension, heart failure and cardiovascular risk guidance.
Reference: HOPE trial; NICE NG136; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
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- Peripheral Arterial Disease · NICE NG19 2012 / ESVS 2017
- Carotid Artery Disease · NICE CG68 / ESVS 2018
- Varicose Veins Management · NICE CG168 2013
- Venous Leg Ulcer Management · NICE NG204 2022
- Acute Heart Failure · ESC 2021 Heart Failure Guidelines; NICE NG106
- NSTEMI / Unstable Angina · ESC 2020 NSTEMI Guidelines; NICE NG185