Ivabradine

Prescription ·Strong evidence ·Reviewed May 2026

Ivabradine selectively reduces heart rate without affecting blood pressure, contractility, or conduction. The SHIFT trial demonstrated reduced heart failure hospitalization in patients with HFrEF and resting HR >=70 bpm on maximally tolerated beta-blocker therapy. It is the only selective sinus node inhibitor approved for heart failure.

What it's good for
  • Reduces heart failure hospitalization (SHIFT trial)6,2
  • Selective heart rate reduction without hemodynamic effects2,3
  • Does not reduce blood pressure or contractility
  • Additive to beta-blocker therapy
What to watch for
  • Bradycardia
  • Luminous phenomena (phosphenes, visual brightness sensations)
  • Atrial fibrillation
  • Resting heart rate <60 bpm before treatment2,3
  • Severe hepatic impairment

The bottom line

Evidence rating strong. Most-documented uses: reduces heart failure hospitalization (shift trial), selective heart rate reduction without hemodynamic effects, does not reduce blood pressure or contractility. 10 sources indexed (2022–2025), with 3 interaction records on file.

The science

How it works, mechanistically.

Core mechanism

Selectively and specifically inhibits the If (funny) current in the sinoatrial node by blocking hyperpolarization-activated cyclic nucleotide-gated (HCN) channels. This slows the rate of diastolic depolarization in pacemaker cells, reducing heart rate without affecting myocardial contractility, blood pressure, or intracardiac conduction. Heart rate reduction is proportional to the baseline rate.3

Class
Hyperpolarization-Activated Cyclic Nucleotide-Gated (HCN) Channel Blocker
Absorption
Water-soluble; take with food
Dosing

Dosing & protocol.

Common range
2.5–7.5 mg twice daily (as prescribed by your physician)
Recommended form
Oral tablet, taken with meals

Take with food; absorption is delayed by food but bioavailability increases by ~20–40%

Safety

Full safety detail.

Side effects

  • Bradycardia
  • Luminous phenomena (phosphenes, visual brightness sensations)
  • Atrial fibrillation
  • Blurred vision
  • Headache
  • Dizziness

Contraindications

  • Resting heart rate <60 bpm before treatment2,3
  • Severe hepatic impairment
  • Acute decompensated heart failure3,2
  • Blood pressure <90/50 mmHg
  • Sick sinus syndrome, sinoatrial block, or third-degree AV block (unless pacemaker present)1,9
  • Concurrent strong CYP3A4 inhibitors (azole antifungals, macrolide antibiotics, HIV protease inhibitors)
  • Pacemaker dependence (HR maintained exclusively by pacemaker)
Interactions

Interaction records.

SeriousCaution

Potassium

Ivabradine lowers heart rate and has rare reports of torsades de pointes when other risk factors are present. Low potassium increases torsades risk with bradycardia and QT-risk drugs. Potassium supplements are not routinely needed with ivabradine, but potassium deficiency should be corrected under monitoring.

Recommendation: Keep potassium in the normal range while using ivabradine, especially during diuretic use, gastrointestinal illness, or addition of other QT-prolonging medicines. Do not self-treat with high-dose potassium unless your clinician is checking blood potassium and kidney function. Report fainting, near-fainting, or new sustained palpitations promptly.

SeriousCaution

Magnesium Glycinate

Ivabradine can cause clinically important bradycardia, and torsades de pointes has been reported when interacting QT-risk drugs are added. Low magnesium is a recognized torsades risk factor in bradycardic or QT-prolonged states. Magnesium is useful when deficiency is present or likely; it should not be used to mask symptoms such as fainting or severe dizziness.

Recommendation: Maintain normal magnesium intake while taking ivabradine, and ask about checking magnesium if you also use diuretics, proton pump inhibitors, or have chronic diarrhea. Avoid high-dose magnesium without monitoring if you have kidney disease. Seek urgent care for fainting, near-fainting, or sustained palpitations.

SeriousConflict

St. John's Wort

St. John's Wort can induce CYP3A4 and P-glycoprotein, and systematic reviews identify ivabradine as a drug whose exposure can be reduced by this herb. Lower ivabradine exposure may reduce heart-rate control and antianginal or heart-failure benefit. The effect can persist after stopping St. John's Wort because enzyme induction takes time to reverse.

Recommendation: Avoid St. John's Wort while taking ivabradine unless your prescriber specifically approves and monitors the combination. Do not use dose spacing as a workaround because this is an enzyme and transporter induction interaction. Tell your clinician if you start or stop St. John's Wort so heart rate, symptoms, and ivabradine dosing can be reassessed.

Sources

Sources, by evidence tier.

Numbered references. Citations throughout the page link here.

Meta-analyses & systematic reviews

5
Keep exploring

Deep dives & adjacent profiles.

This page is educational. Do not start, stop, or change a supplement or medication based on it without checking with a qualified healthcare professional.

Use this with your stack

Ivabradine in NutriStack.

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NutriStack is an informational and organizational tool, not a medical service, and not a substitute for professional advice. Always consult a qualified healthcare professional before starting, stopping, or changing any supplement or medication.