Ivabro

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January 30, 2026 / IvabroDescription Ivabradine HCl is a unique medication that is classified as a hyperpolarization-activated cyclic nucleotide-gated (HCN) channel blocker or, more simply, an If​ channel inhibitor. Unlike beta-blockers or calcium channel blockers, ivabradine lowers heart rate without affecting blood pressure or myocardial contractility (the force of the heart’s contraction). The “HCl” in […]

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SKU: Ivabradine HCl
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Description

January 30, 2026 /

Ivabro

Description

Ivabradine HCl is a unique medication that is classified as a hyperpolarization-activated cyclic nucleotide-gated (HCN) channel blocker or, more simply, an If​ channel inhibitor. Unlike beta-blockers or calcium channel blockers, ivabradine lowers heart rate without affecting blood pressure or myocardial contractility (the force of the heart’s contraction). The “HCl” in its name denotes the hydrochloride salt form, which is used for stability and solubility.

Indications

Ivabradine is primarily indicated for the treatment of two conditions, both related to its ability to slow the heart rate:

  • Symptomatic Stable Angina Pectoris: It is used to treat chronic stable angina in adults with a normal sinus rhythm who have a heart rate of at least 70 beats per minute. It is typically used for patients who cannot tolerate or have contraindications to beta-blockers, or in combination with beta-blockers if their angina is not adequately controlled.

  • Chronic Heart Failure: It is used in adults with chronic systolic heart failure (NYHA class II to IV) with a normal sinus rhythm and a heart rate of at least 75 beats per minute, in combination with standard therapy, including beta-blocker therapy, or when beta-blocker therapy is contraindicated or not tolerated.

Mechanism of Action

Ivabradine’s mechanism of action is highly specific and differs from other cardiovascular drugs. It works by selectively inhibiting the If​ channel, also known as the “funny current” channel

If​ Channel Inhibition: The If​ channel is found in the sinoatrial (SA) node, the natural pacemaker of the heart. These channels are responsible for generating the slow inward current that drives the spontaneous depolarization of the SA node cells. This depolarization is what sets the heart’s rhythm and rate.

  1. Slowing the Pacemaker: By selectively blocking these If​ channels, ivabradine slows down this spontaneous depolarization process.
  2. Heart Rate Reduction: This results in a reduction in the firing rate of the SA node, which directly translates to a slower heart rate.

  3. No Effect on Blood Pressure or Contractility: Because ivabradine’s action is confined to the If​ channels in the SA node, it does not affect the calcium or potassium channels responsible for myocardial contractility or vascular smooth muscle tone. This means it can lower the heart rate without causing a drop in blood pressure or a decrease in the force of the heart’s contraction, which are common effects of beta-blockers and calcium channel blockers.

This unique mechanism makes ivabradine an excellent option for patients who need heart rate control but have conditions where a drop in blood pressure or reduced heart contractility would be undesirable.

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