Product image of Labetalol S.A.L.F. (Labetalol Hydrochloride) supplied by GNH India

Labetalol S.A.L.F.

Active Ingredient:
Labetalol Hydrochloride
Origin:
EU

Labetalol S.A.L.F. (Labetalol Hydrochloride)

Labetalol Hydrochloride, the active ingredient in Labetalol S.A.L.F., is a non-selective beta blocker with alpha‑1 blocking activity presented as an injectable solution for intravenous use. It is employed to rapidly lower blood pressure in hypertensive emergencies, severe hypertension, and preeclampsia.

GNH India supplies Labetalol S.A.L.F. as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

S.A.L.F. Spa Laboratorio Farmacologico

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Indications & Clinical Uses

  • Labetalol is used in the management of acute elevations in blood pressure that require prompt control.
  • Hypertensive emergencies: rapid reduction of dangerously high blood pressure to prevent organ damage.
  • Severe hypertension: sustained lowering of elevated arterial pressure when oral therapy is insufficient.
  • Preeclampsia: control of maternal hypertension to reduce risk to mother and fetus.

How It Works

  • Labetalol blocks alpha‑1 adrenergic receptors, causing vasodilation, while simultaneously antagonizing beta‑1 and beta‑2 receptors, which decreases heart rate and myocardial contractility. The combined effect reduces peripheral vascular resistance and cardiac output, leading to a prompt fall in arterial blood pressure.

Side Effects

Labetalol may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Dizziness: sensation of light‑headedness, especially after dose initiation.
  • Headache: mild to moderate pain often transient.
  • Nausea: upset stomach, sometimes accompanied by vomiting.
  • Flushing: warm, reddened skin, usually on the face or neck.

Serious or Rare Side Effects

  • Severe hypotension: abrupt, marked drop in blood pressure requiring medical intervention.
  • Bronchospasm: constriction of airways, particularly in patients with reactive airway disease.
  • Hepatic dysfunction: elevated liver enzymes or jaundice.
  • Cardiac conduction abnormalities: heart block or arrhythmias that may be life‑threatening.

Precautions & Warnings

  • Before using Labetalol, clinicians should consider several safety measures.
  • Monitor blood pressure: avoid excessive reductions that could cause syncope.
  • Assess cardiac function: use cautiously in patients with bradycardia or heart block.
  • Check liver function: dose adjustments may be needed in hepatic impairment.
  • Avoid abrupt discontinuation: taper gradually if therapy has been long‑term.
  • Pregnancy: prescribe only when the potential benefit justifies the potential risk to the fetus.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Labetalol can interact with other medicines, altering its efficacy or safety.

Major Interactions (Avoid)

  • Other beta‑blockers: additive bradycardia and hypotension.
  • Calcium channel blockers (e.g., verapamil): increased risk of severe hypotension.
  • Epinephrine: reduced vasoconstrictive response, potentially compromising emergency treatment.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may blunt antihypertensive effect.
  • Diuretics: can potentiate hypotensive response.
  • CYP2D6 inhibitors (e.g., fluoxetine): may raise labetalol plasma concentrations.
  • Anesthetic agents: enhanced cardiovascular depression during surgery.

Frequently Asked Questions

Labetalol S.A.L.F. is indicated for the rapid control of blood pressure in hypertensive emergencies, severe hypertension, and preeclampsia. It is administered intravenously in hospital settings to quickly lower arterial pressure and reduce the risk of organ damage.

Labetalol Hydrochloride blocks alpha‑1 receptors, causing blood‑vessel dilation, while also antagonizing beta‑1 and beta‑2 receptors, which reduces heart rate and contractility. The combined effect decreases peripheral vascular resistance and cardiac output, leading to a fall in blood pressure.

The specific dose and infusion rate are determined by the prescribing clinician based on the patient’s clinical condition, response, and monitoring parameters. Dosing is individualized and should follow local protocols and the prescriber’s judgment.

Safety data for Labetalol in pregnancy and lactation are limited. It may be used during pregnancy only when the potential benefit justifies the potential risk to the fetus, and breastfeeding decisions should be made in consultation with a healthcare professional.

To place an order, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed) and import documentation.

Labetalol’s unique combination of alpha‑1 and non‑selective beta‑blocking activity allows simultaneous vasodilation and reduction of cardiac output, which can be advantageous over agents that target only one pathway. Compared with pure beta‑blockers, it may achieve faster blood‑pressure control in emergencies, but the choice depends on patient‑specific factors.

Labetalol S.A.L.F. should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the vial in its original packaging until use and discard any solution that appears discolored or contains particles.

The product is supplied as an injectable solution for intravenous administration. It is typically given as a slow IV push or infusion under continuous blood‑pressure monitoring in a clinical setting, following the prescriber’s dosing instructions.

Serious risks include severe hypotension, bronchospasm in patients with reactive airway disease, hepatic dysfunction, and cardiac conduction abnormalities such as heart block. Prompt recognition and management of these events are essential.

Labetalol is contraindicated in patients with known hypersensitivity to labetalol or any component of the formulation, in those with severe bradycardia, second‑ or third‑degree heart block without a pacemaker, and in patients with uncompensated heart failure or cardiogenic shock.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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