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Potassium channel activator with nitrate component Pregnancy: There are no or limited data in pregnant women; as a precautionary measure it is preferable to avoid use during pregnancy. Not recommended during breast-feeding (excreted in small amounts into animal breast milk; human excretion unknown). Insufficient fertility data to estimate human risk.

Nicorandil

Brand names: Ikorel

Nicorandil is a potassium-channel-activator anti-anginal used when standard agents are insufficient or not tolerated.

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: 10 mg twice daily (usual starting dose); usual therapeutic range 10 to 20 mg twice daily
Route: Oral — swallow whole with a glass of water; do not crush or chew (the tablet can be divided into equal doses). Administration is independent of food intake
Frequency: Twice daily, preferably in the morning and in the evening
Max: 40 mg twice daily
eMC §4.2. It is recommended that the dose be titrated upwards in accordance with the patient's needs, response and tolerance, up to 40 mg twice daily if necessary. A lower starting dose of 5 mg twice daily may be used in patients particularly prone to headache (headache occurs in more than 30% of patients, particularly in the first days of treatment; progressive dose titration may reduce its frequency). Elderly: no special dose requirements, but as with all medicines use of the lowest effective dose is recommended. Liver and/or renal impairment: no special dosage requirements. Paediatric population: not recommended in paediatric patients since safety and efficacy have not been established in this group — no paediatric dose is given; refer to a children's formulary. Safety warning from §4.4: nicorandil-induced gastrointestinal, skin, mucosal and eye ulcerations may occur at different locations in the same patient, are refractory to treatment and mostly respond only to withdrawal — if ulceration develops, nicorandil should be discontinued. Onset ranges from shortly after initiation to several years later.

Dose adjustments

Renal

No special dosage requirements for patients with liver and/or renal impairment; however, use with care in combination with other products that may increase potassium levels, especially in moderate to severe renal impairment.

Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.

Contraindications

  • Hypersensitivity to nicorandil or to any of the excipients
  • Shock (including cardiogenic shock), severe hypotension, or left ventricular dysfunction with low filling pressure, or cardiac decompensation
  • Use of phosphodiesterase 5 inhibitors (risk of a serious drop in blood pressure)
  • Use of soluble guanylate cyclase stimulators (such as riociguat) — risk of a serious fall in blood pressure
  • Hypovolaemia
  • Acute pulmonary oedema

Side effects

  • Very common: headache (reported in more than 30% of patients in clinical trials, particularly in the first days of treatment)
  • Common: dizziness; cutaneous vasodilation with flushing; nausea and vomiting; feeling of weakness; decrease in blood pressure; heart rate increased
  • Gastrointestinal ulcerations (stomatitis, aphthosis, mouth, tongue, small intestinal, large intestinal and anal ulcers), gastrointestinal haemorrhage and diverticulitis — may progress to perforation, fistula or abscess formation
  • Skin and mucosal ulcerations (mainly peri-anal, genital and parastomal), rash, pruritus; angioedema (rare)
  • Eye disorders: corneal ulcer, conjunctival ulcer, conjunctivitis; diplopia; ophthalmoplegia and IIIrd/VIth nerve paralysis (often associated with headache)
  • Hyperkalaemia; myalgia; liver disorders such as hepatitis, cholestasis or jaundice

Interactions

  • Phosphodiesterase 5 inhibitors — contraindicated; serious drop in blood pressure
  • Soluble guanylate cyclase stimulators e.g. riociguat — contraindicated; serious fall in blood pressure
  • Acetylsalicylic acid or NSAIDs — increased risk of severe complications such as gastrointestinal haemorrhage secondary to nicorandil-induced ulceration; caution advised
  • Corticosteroids — gastrointestinal perforations reported with concomitant use; caution advised
  • Other medicinal products with a blood-pressure-lowering effect — caution advised
  • Other medicinal products that may increase potassium levels — risk of severe hyperkalaemia, especially in moderate to severe renal impairment
  • NOTE: eMC §4.5 was not captured in this bundle — the interactions above are taken from §4.3 and §4.4, which cross-refer to §4.5. Clinician to review the full §4.5 before publication.

Clinical monograph

How it works

It combines nitrate-like venodilation with arterial dilation through potassium-channel opening, reducing cardiac preload/afterload and improving coronary blood flow.

Prescribing in practice

  • It can cause serious ulceration of skin, mucosa and the gastrointestinal tract (mouth, anal and gastrointestinal ulcers, fistulae or perforation) — investigate any ulceration and usually stop the drug.
  • Headache is common early in treatment.
  • It is contraindicated with phosphodiesterase-5 inhibitors (e.g. sildenafil) and in significant hypotension.

Monitoring

Review for ulceration at any site and for blood pressure/headache.

Counselling the patient

  • Report any persistent mouth, skin, anal or gut ulcers — they can be caused by this medicine.
  • Do not take erectile-dysfunction drugs such as sildenafil with it.
  • Headaches at the start often settle.

Evidence & guidelines

An add-on anti-anginal in stable angina (NICE NG185 pathway), with an important ulceration warning.

Reference: NICE CG126; MHRA Drug Safety Update; 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.