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, the active ingredient in Labetalol S.A.L.F., is an alpha/beta adrenergic antagonist presented as an intravenous solution for parenteral use. It is employed to manage hypertension and hypertensive emergencies in adult patients.
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 an antihypertensive agent that acts on both alpha‑1 and beta‑adrenergic receptors to lower blood pressure.

  • Hypertension: provides sustained reduction of systemic arterial pressure in chronic hypertension.
  • Hypertensive emergencies: enables rapid blood pressure control in acute severe hypertension.
  • Pregnancy‑induced hypertension: offers safe blood pressure management when other agents are contraindicated.

How It Works

  • Labetalol exerts a non‑selective blockade of beta‑adrenergic receptors (β1 and β2) together with a selective antagonism of alpha‑1 receptors. This dual action reduces cardiac output through decreased heart rate and contractility while also lowering peripheral vascular resistance, resulting in an overall decline in arterial blood pressure.

Side Effects

Labetalol may cause a range of adverse reactions, some of which are more frequent than others.

Common Side Effects

  • Dizziness: sensation of light‑headedness, especially after dose changes.
  • Headache: mild to moderate intensity, often transient.
  • Fatigue: generalized tiredness without exertion.
  • Nausea: occasional upset stomach or urge to vomit.
  • Flushing: warm sensation and reddening of the skin.
  • Nasal congestion: feeling of blocked nasal passages.

Serious or Rare Side Effects

  • Severe hypotension: dangerously low blood pressure requiring medical intervention.
  • Bronchospasm: narrowing of airways, particularly in patients with asthma.
  • Hepatic dysfunction: elevated liver enzymes or jaundice.
  • Cardiac conduction abnormalities: heart block or arrhythmias.
  • Stevens‑Johnson syndrome: rare severe skin reaction.
  • Acute heart failure: worsening of cardiac function in susceptible individuals.

Precautions & Warnings

When using Labetalol, clinicians should observe several safety measures.

  • Blood pressure monitoring: check regularly to avoid excessive hypotension.
  • Asthma caution: use carefully in patients with reactive airway disease due to possible bronchospasm.
  • Hepatic impairment: consider dose adjustment or alternative therapy in liver disease.
  • Abrupt discontinuation: avoid sudden stop to prevent rebound hypertension.
  • Renal dysfunction: monitor renal function and adjust dosing as needed.
  • Store at ambient temperature: keep in original container, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • MAO inhibitors: risk of severe hypertension.
  • Other antihypertensives: additive hypotensive effect.
  • Additional beta‑blockers: excessive bradycardia or heart block.
  • Calcium channel blockers: heightened blood pressure lowering.
  • Clonidine: possible rebound hypertension on withdrawal.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may diminish antihypertensive response.
  • Diuretics: can cause electrolyte imbalances.
  • Insulin or oral hypoglycemics: may mask hypoglycemia symptoms.
  • Anesthetic agents: may potentiate cardiovascular depression.
  • Certain antidepressants: monitor for altered blood pressure control.

Frequently Asked Questions

Labetalol S.A.L.F. is indicated for the treatment of hypertension and hypertensive emergencies. It may also be employed in managing pregnancy‑induced hypertension when other therapies are unsuitable, providing blood pressure control through its combined alpha‑ and beta‑blocking actions.

Labetalol blocks beta‑adrenergic receptors, reducing heart rate and contractility, while simultaneously antagonizing alpha‑1 receptors, which dilates blood vessels. This dual mechanism decreases cardiac output and peripheral vascular resistance, leading to an overall reduction in arterial pressure.

The specific dose of Labetalol S.A.L.F. is determined by the prescribing healthcare professional based on the patient’s condition, severity of hypertension, and response to therapy. Dosage adjustments are made according to clinical judgment and monitoring.

Safety data for labetalol in pregnancy and lactation are limited. It may be used during pregnancy when the benefits outweigh potential risks, particularly for severe hypertension. Breastfeeding considerations should be discussed with a healthcare provider, as the drug can be excreted in milk.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request trade or institutional credentials before providing pricing, availability, shipping details and any necessary import documentation.

Labetalol’s unique combination of alpha‑ and beta‑blocking effects distinguishes it from agents that target only one receptor type. Compared with pure beta‑blockers, it offers additional vasodilation, and versus pure alpha‑blockers, it provides heart‑rate control, making it useful in situations requiring rapid, balanced blood pressure reduction.

Labetalol S.A.L.F. should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the product from moisture, direct sunlight, and extreme temperature fluctuations to maintain stability and potency.

Labetalol S.A.L.F. is administered intravenously by a qualified healthcare professional. The infusion rate and concentration are adjusted according to the patient’s blood pressure response, with continuous monitoring to ensure safe and effective therapy.

Serious risks include severe hypotension, bronchospasm in patients with reactive airway disease, hepatic dysfunction, and cardiac conduction abnormalities such as heart block. Immediate medical attention is required if any of these adverse events occur.

Labetalol S.A.L.F. is contraindicated in patients with known hypersensitivity to labetalol, severe bradycardia, second‑ or third‑degree heart block without a pacemaker, and in those with uncontrolled asthma or severe chronic obstructive pulmonary disease due to the risk of bronchospasm.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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