Profound and prolonged systemic hypotension, syncope.
Concomitant use is absolutely contraindicated. Patients on nicorandil should not be prescribed riociguat.
Vasodilator · Antianginal
Nicorandil has a unique dual mechanism: it opens ATP-sensitive potassium channels (K-ATP) in vascular smooth muscle, causing hyperpolarization and vasodilation of arterioles (reducing afterload), and it possesses a nitrate moiety that releases nitric oxide, dilating capacitance veins (reducing preload) and epicardial coronary arteries. This combination of arteriolar and venodilator effects reduces both preload and afterload while improving coronary blood flow. The IONA trial demonstrated that nicorandil reduces major adverse coronary events in stable angina.
Profound and prolonged systemic hypotension, syncope.
Concomitant use is absolutely contraindicated. Patients on nicorandil should not be prescribed riociguat.
Extreme hypotension, potentially life-threatening.
PDE5 inhibitors should not be prescribed to patients receiving any form of nitrate. Patients should be warned not to use PDE5 inhibitors and nitrates concurrently. No PDE5 inhibitor should be used in the 24 hours prior to initiating nitrate therapy. If significant hypotension occurs, fluids and α adrenergic receptor agonists may be used for support.
Profound and prolonged systemic hypotension, syncope, myocardial ischemia, and even death.
Concomitant use is absolutely contraindicated. Patients on nicorandil should not be prescribed tadalafil or other PDE5 inhibitors (sildenafil, vardenafil).
Profound and prolonged systemic hypotension, syncope, myocardial ischemia, and even death.
Concomitant use is absolutely contraindicated. Patients on nicorandil should not be prescribed vardenafil or other PDE5 inhibitors (sildenafil, tadalafil).
Additive hypotensive effects, potentially leading to severe hypotension, dizziness, syncope, and reflex tachycardia.
Avoid concomitant use if possible. If co-administration is necessary, monitor blood pressure closely and consider reducing the dose of one or both agents. Educate the patient about symptoms of hypotension.
Additive hypotensive effects, potentially leading to severe hypotension, dizziness, syncope, and reflex tachycardia.
Avoid concomitant use if possible. If co-administration is necessary, monitor blood pressure closely and consider reducing the dose of one or both agents. Educate the patient about symptoms of hypotension.
Additive hypotensive effects, potentially leading to severe hypotension, dizziness, syncope, and reflex tachycardia.
Avoid concomitant use if possible. If co-administration is necessary, monitor blood pressure closely and consider reducing the dose of one or both agents. Educate the patient about symptoms of hypotension.
Additive hypotensive effects, potentially leading to symptomatic hypotension, dizziness, and syncope.
Monitor blood pressure closely, especially during initiation or dose titration of either drug. Consider starting with lower doses of both agents or adjusting doses based on blood pressure response. Educate the patient about symptoms of hypotension.
Additive hypotensive effects, potentially leading to symptomatic hypotension, dizziness, and syncope, especially in volume-depleted patients.
Monitor blood pressure and hydration status closely. Adjust doses of either drug as needed. Ensure adequate hydration. Educate the patient about symptoms of hypotension.
Additive hypotensive effects, potentially leading to symptomatic hypotension, dizziness, and syncope. However, beta-blockers can also counteract reflex tachycardia induced by nicorandil.
Monitor blood pressure closely, especially during initiation or dose titration of either drug. Adjust doses as needed. Educate the patient about symptoms of hypotension.
Additive hypotensive effects, potentially leading to symptomatic hypotension, dizziness, and syncope.
Monitor blood pressure closely, especially during initiation or dose titration of either drug. Consider starting with lower doses of both agents or adjusting doses based on blood pressure response. Educate the patient about symptoms of hypotension.
Potentially increased risk of bleeding, although typically mild and not well-documented as a significant interaction.
Monitor for signs of bleeding (e.g., bruising, epistaxis). Generally, co-administration is safe and often indicated in cardiovascular patients. No dose adjustment is usually required unless other risk factors for bleeding are present.
Continue into a citation-backed clinical answer with the drug context already attached.
Sources: KD Tripathi 7e, Goodman & Gilman 14e, Harrison 22e, Katzung·Verified: 2026-05-10 · House clinical team