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ACE Inhibitor Pregnancy: Not recommended during the first trimester and contraindicated during the second and third trimesters. Exposure from the second trimester induces human foetotoxicity (decreased renal function, oligohydramnios, skull ossification retardation) and neonatal toxicity (renal failure, hypotension, hyperkalaemia); if exposure has occurred, ultrasound check of renal function and skull is recommended and newborns should be observed for hypotension, oliguria and hyperkalaemia. Not recommended during breast-feeding.

Ramipril

Brand names: Tritace

Ramipril is an ACE inhibitor used for hypertension, heart failure, and cardiovascular and renal protection; this page focuses on its use in older people.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: Hypertension: initial 2.5 mg once daily (1.25 mg once daily in patients with a strongly activated renin-angiotensin-aldosterone system, and in hypertensive patients in whom a concurrent diuretic is not discontinued). The dose can be doubled at intervals of two to four weeks to progressively achieve the target blood pressure
Route: Oral (swallow with liquid; must not be chewed or crushed; may be taken before, with or after meals)
Frequency: Once daily
Max: 10 mg daily
ELDERLY: initial doses should be lower and subsequent titration more gradual because of the greater chance of undesirable effects, especially in very old and frail patients; a reduced initial dose of 1.25 mg ramipril should be considered. Diuretic-treated patients: hypotension is more likely; if possible discontinue the diuretic 2-3 days before starting ramipril, otherwise start at 1.25 mg and monitor renal function and serum potassium. OTHER INDICATIONS: Cardiovascular prevention - 2.5 mg once daily, double after one or two weeks and, after another two to three weeks, increase to the target maintenance dose of 10 mg once daily. Diabetes with microalbuminuria, and non-diabetic nephropathy with macroproteinuria of 3 g/day or more - 1.25 mg once daily, doubled to 2.5 mg after two weeks and then to 5 mg after a further two weeks. Diabetes with at least one cardiovascular risk factor - 2.5 mg once daily, doubled to 5 mg after one or two weeks and then to 10 mg after a further two or three weeks (target 10 mg daily). Symptomatic heart failure (patients stabilised on diuretic therapy) - initial 1.25 mg daily, titrated by doubling every one to two weeks up to a maximum of 10 mg daily, preferably in two administrations per day. Secondary prevention after acute myocardial infarction with heart failure - starting 48 hours after the infarct in a clinically and haemodynamically stable patient, 2.5 mg twice daily for three days (if not tolerated, 1.25 mg twice daily for two days before increasing to 2.5 mg then 5 mg twice daily); thereafter double the dose at intervals of one to three days to the target maintenance dose of 5 mg twice daily; withdraw treatment if the dose cannot be increased to 2.5 mg twice daily. Experience is lacking in severe (NYHA IV) heart failure immediately after myocardial infarction - if treated, start at 1.25 mg once daily with particular caution on any dose increase. Hepatic impairment: initiate only under close medical supervision; maximum daily dose 2.5 mg. NOTE: the fetched eMC bundle did not include §4.5, so the interaction list below is drawn from §4.3, §4.4 and the US label and is not a complete interaction profile.

Dose adjustments

Renal

Base the daily dose on creatinine clearance: CrCl 60 ml/min or above - no adjustment to the initial dose (2.5 mg/day), maximum 10 mg/day; CrCl 30-60 ml/min - initial dose unchanged (2.5 mg/day), maximum 5 mg/day; CrCl 10-30 ml/min - initial 1.25 mg/day, maximum 5 mg/day; haemodialysed hypertensive patients (ramipril is slightly dialysable) - initial 1.25 mg/day, maximum 5 mg/day, administered a few hours after haemodialysis.

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 ramipril, to any excipient or to any other ACE inhibitor
  • History of angioedema (hereditary, idiopathic, or due to previous angioedema with ACE inhibitors or angiotensin II receptor antagonists)
  • 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 below 60 ml/min/1.73 m2)

Side effects

  • Non-productive tickling cough
  • Headache and dizziness
  • Hypotension, orthostatic blood pressure decrease and syncope
  • Blood potassium increased
  • Gastrointestinal inflammation, digestive disturbance, dyspepsia, diarrhoea, nausea, vomiting
  • Angioedema (serious - including small bowel angioedema); rash
  • Renal or hepatic impairment; neutropenia/agranulocytosis (rare)

Interactions

  • Sacubitril/valsartan - concomitant use contraindicated (angioedema risk); observe the required washout between the two
  • Aliskiren-containing products - contraindicated in diabetes mellitus or renal impairment (GFR below 60 ml/min/1.73 m2)
  • Dual RAAS blockade with angiotensin II receptor blockers or aliskiren - not recommended (increased hypotension, hyperkalaemia and renal impairment); ACE inhibitors and ARBs must not be used together in diabetic nephropathy
  • Diuretics - possibility of excessive hypotension, especially when recently started; reduce or stop the diuretic, or reduce the ramipril starting dose
  • Potassium-sparing diuretics (spironolactone, amiloride, triamterene), potassium supplements and potassium-containing salt substitutes - increased risk of hyperkalaemia; monitor serum potassium frequently
  • NSAIDs - increased risk of renal impairment and loss of antihypertensive effect
  • Lithium - use with caution
  • Gold (injectable) - nitritoid reactions have been reported

Clinical monograph

How it works

It inhibits angiotensin-converting enzyme, reducing angiotensin II formation and aldosterone, causing vasodilatation and lowering blood pressure and cardiac afterload.

Prescribing in practice

  • In older people start at a low dose and uptitrate cautiously, as they are more prone to first-dose and symptomatic hypotension, acute kidney injury and hyperkalaemia, particularly with volume depletion, renovascular disease or concurrent NSAIDs or diuretics.
  • Check renal function and potassium before starting and after dose changes; stop if there is a significant rise in creatinine or potassium.
  • It is contraindicated in pregnancy and in those with a history of ACE-inhibitor angioedema.

Monitoring

Monitor blood pressure, renal function and serum potassium at baseline, after initiation and following each dose increase, especially in older patients.

Counselling the patient

  • A dry cough can occur and may warrant switching to an alternative.
  • Report dizziness, or swelling of the face, lips or tongue, urgently.
  • Avoid over-the-counter anti-inflammatory painkillers without advice.

Evidence & guidelines

Landmark trials including HOPE established ramipril's cardiovascular benefit, and NICE supports ACE inhibitors across hypertension and heart failure with cautious titration in older adults.

Reference: NICE NG136 (Hypertension); NICE NG106 (Chronic Heart Failure); HOPE Trial; 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.