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.
Adult dose
Dose adjustments
Daily dose should be based on creatinine clearance: CrCl >= 60 ml/min - no adjustment of the initial dose (2.5 mg/day), maximal daily dose 10 mg. CrCl 30-60 ml/min - no adjustment of the initial dose (2.5 mg/day), maximal daily dose 5 mg. CrCl 10-30 ml/min - initial dose 1.25 mg/day, maximal daily dose 5 mg. Haemodialysed hypertensive patients - ramipril is slightly dialysable; initial dose 1.25 mg/day, maximal daily dose 5 mg, administered a few hours after haemodialysis is performed.
Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.
Contraindications
- Hypersensitivity to the active substance, to any of the excipients, or to any other ACE inhibitor
- History of angioedema (hereditary, idiopathic, or due to previous angioedema with ACE inhibitors or AIIRAs)
- Concomitant use with sacubitril/valsartan therapy
- Extracorporeal treatments leading to contact of blood with negatively charged surfaces
- Significant bilateral renal artery stenosis, or renal artery stenosis in a single functioning kidney
- Second and third trimesters of pregnancy
- Hypotensive or haemodynamically unstable states
- Concomitant use with aliskiren-containing products in patients with diabetes mellitus or renal impairment (GFR < 60 ml/min/1.73m2)
Side effects
- Non-productive tickling cough (common); also bronchitis, sinusitis and dyspnoea
- Headache and dizziness (common); vertigo, paraesthesia, dysgeusia and tremor (uncommon)
- Hypotension, orthostatic blood pressure decreased and syncope (common)
- Gastrointestinal inflammation, digestive disturbances, abdominal discomfort, dyspepsia, diarrhoea, nausea and vomiting (common)
- Blood potassium increased (common); rash, in particular maculo-papular (common); angioedema (serious - can be life-threatening), renal or hepatic impairment, pancreatitis, severe skin reactions and neutropenia/agranulocytosis are listed as serious adverse reactions
Interactions
- Sacubitril/valsartan - concomitant use contraindicated
- Aliskiren-containing products - contraindicated in patients with diabetes mellitus or renal impairment (GFR < 60 ml/min/1.73m2)
- Angiotensin II receptor blockers or aliskiren (dual RAAS blockade) - not recommended; increased risk of hypotension, hyperkalaemia and decreased renal function including acute renal failure. ACE inhibitors and ARBs should not be used concomitantly in patients with diabetic nephropathy
- Extracorporeal treatments leading to contact of blood with negatively charged surfaces - contraindicated
- Diuretics - hypotension may occur on initiation, particularly in volume- or salt-depleted patients; if possible discontinue the diuretic 2-3 days beforehand, otherwise start ramipril at 1.25 mg with monitoring of renal function and serum potassium
- Agents producing hypotension during anaesthesia/major surgery - risk of an acute pronounced fall in blood pressure
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. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
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- Acute Heart Failure · ESC 2021 Heart Failure Guidelines; NICE NG106
- NSTEMI / Unstable Angina · ESC 2020 NSTEMI Guidelines; NICE NG185