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ACE Inhibitor Pregnancy: Not recommended during the first trimester of pregnancy and CONTRAINDICATED during the second and third trimesters. ACE inhibitors should not be initiated during pregnancy; patients planning pregnancy should be changed to alternative antihypertensives with an established safety profile, and treatment should be stopped immediately when pregnancy is diagnosed. Second- and third-trimester exposure is known to cause foetotoxicity (decreased renal function, oligohydramnios, skull ossification retardation) and neonatal toxicity (renal failure, hypotension, hyperkalaemia); newborns exposed should be closely observed for hypotension, oliguria and hyperkalaemia. Breast-feeding: not recommended - alternative treatments with better established safety profiles are preferable, especially while nursing a newborn or preterm infant.

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.

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: 2.5 mg once daily initially (hypertension and cardiovascular prevention), titrated to a maintenance/target dose of up to 10 mg once daily
Route: Oral - swallowed with liquid; must not be chewed or crushed; may be taken before, with or after meals, at the same time each day
Frequency: Once daily (heart failure and post-myocardial-infarction regimens are given twice daily - see notes)
Max: 10 mg daily
Source: UK SPC (eMC) section 4.2 for Ramipril 10mg Tablets (https://www.medicines.org.uk/emc/product/8067/smpc). HYPERTENSION - VERBATIM: 'Ramipril should be started gradually with an initial recommended dose of 2.5 mg daily... A starting dose of 1.25 mg is recommended in [patients with a strongly activated renin-angiotensin-aldosterone system] and the initiation of treatment should take place under medical supervision... The dose can be doubled at interval of two to four weeks to progressively achieve target blood pressure; the maximum permitted dose of Ramipril is 10 mg daily. Usually the dose is administered once daily.' CARDIOVASCULAR PREVENTION: initial 2.5 mg once daily; double the dose after one or two weeks and, after another two to three weeks, increase to the target maintenance dose of 10 mg once daily, depending on tolerability. DIURETIC-TREATED PATIENTS: if possible discontinue the diuretic 2-3 days before starting ramipril; if the diuretic is not discontinued in hypertensive patients, initiate at 1.25 mg and monitor renal function and serum potassium. DIABETES WITH MICROALBUMINURIA: initial 1.25 mg once daily, doubling to 2.5 mg after two weeks then 5 mg after a further two weeks. DIABETES WITH AT LEAST ONE CARDIOVASCULAR RISK: initial 2.5 mg once daily, doubling to 5 mg after one or two weeks then 10 mg after a further two or three weeks; target daily dose 10 mg. NON-DIABETIC NEPHROPATHY (macroproteinuria >= 3 g/day): initial 1.25 mg once daily, doubling to 2.5 mg after two weeks then 5 mg after a further two weeks. SYMPTOMATIC HEART FAILURE: in patients stabilised on diuretic therapy, initial 1.25 mg daily, titrated by doubling the dose every one to two weeks up to a maximum daily dose of 10 mg; two administrations per day are preferable. SECONDARY PREVENTION AFTER ACUTE MI WITH HEART FAILURE: starting 48 hours after myocardial infarction in a clinically and haemodynamically stable patient, 2.5 mg twice daily for three days; if the initial 2.5 mg dose is not tolerated, give 1.25 mg twice a day for two days before increasing to 2.5 mg then 5 mg twice a day; thereafter double the daily dose at intervals of one to three days up to the target maintenance dose of 5 mg twice daily; if the dose cannot be increased to 2.5 mg twice a day the treatment should be withdrawn. Sufficient 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. ELDERLY: lower initial doses and more gradual titration because of a greater chance of undesirable effects, especially in very old and frail patients - a reduced initial dose of 1.25 mg should be considered. PAEDIATRIC: safety and efficacy in children has not yet been established and no specific recommendation on posology can be made. Note: the UK section 4.5 was not retrieved in this bundle - the interactions below come from the section 4.2, 4.3 and 4.4 text.

Dose adjustments

Renal

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.