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

Labetalolo S.A.L.F.

Active Ingredient:
Labetalol Hydrochloride
Origin:
EU

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

Labetalol, the active ingredient in Labetalolo S.A.L.F., is a beta blocker presented as an intravenous solution for parenteral use. It is employed to manage hypertension, including hypertensive emergencies, by reducing peripheral vascular resistance and cardiac output, providing rapid blood pressure control in adult patients who need immediate therapy.

GNH India supplies Labetalolo S.A.L.F. as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and pharmacies worldwide, ensuring quality and regulatory compliance for critical care settings through reliable logistics and dedicated support teams.

Manufacturer / TM Owner

S.A.L.F. Spa Laboratorio Farmacologico

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Indications & Clinical Uses

Labetalolo S.A.L.F. acts on the cardiovascular system to lower elevated blood pressure.

  • Hypertension: lowers systemic blood pressure by decreasing peripheral vascular resistance and cardiac output.
  • Hypertensive emergencies: provides rapid blood pressure reduction in acute, life‑threatening situations.
  • Angina pectoris: helps relieve chest pain by reducing myocardial oxygen demand through combined alpha‑ and beta‑blockade.

How It Works

  • Labetalol blocks alpha‑1 adrenergic receptors and non‑selective beta‑adrenergic receptors, resulting in vasodilation and reduced heart rate and contractility. This dual antagonism decreases peripheral vascular resistance and cardiac output, leading to a net reduction in arterial blood pressure.

Side Effects

Labetalolo S.A.L.F. may cause a range of adverse reactions.

Common Side Effects

  • Dizziness: feeling light‑headed or unsteady.
  • Fatigue: unusual tiredness or lack of energy.
  • Headache: mild to moderate head pain.
  • Nausea: upset stomach or urge to vomit.
  • Flushing: warmth and redness of the face or neck.
  • Nasal congestion: blocked or runny nose.

Serious or Rare Side Effects

  • Severe hypotension: dangerously low blood pressure requiring medical attention.
  • Bronchospasm: narrowing of the airways, especially in patients with asthma.
  • Hepatic dysfunction: abnormal liver enzyme elevations.
  • Cardiac block: impaired electrical conduction of the heart.
  • Arrhythmias: irregular heart rhythms that may be life‑threatening.
  • Stevens‑Johnson syndrome: severe skin reaction with blistering.

Precautions & Warnings

Before using Labetalolo S.A.L.F., consider the following precautions.

  • Monitor blood pressure: avoid excessive drops that could cause dizziness or syncope.
  • Assess cardiac function: use cautiously in patients with heart failure or conduction disorders.
  • Check respiratory status: avoid in patients with active asthma or severe chronic obstructive pulmonary disease.
  • Review hepatic function: dose adjustment may be needed in liver impairment.
  • Avoid abrupt discontinuation: taper under medical supervision to prevent rebound hypertension.
  • Store below 25°C: keep in original container, protect from light and moisture.

Avoid Interactions

Labetalolo S.A.L.F. can interact with several medicines.

Major Interactions (Avoid)

  • Combined use with other antihypertensives (e.g., ACE inhibitors, diuretics) may cause severe hypotension.
  • Concomitant beta‑agonists (e.g., albuterol) may reduce bronchodilator effectiveness.
  • Co‑administration with calcium‑channel blockers (e.g., verapamil) may increase risk of bradycardia.

Moderate Interactions (Monitor Closely)

  • NSAIDs may blunt the antihypertensive effect of labetalol.
  • Clonidine may cause rebound hypertension if stopped abruptly while on labetalol.
  • Insulin or oral hypoglycemics may have altered glucose control when combined with labetalol.

Frequently Asked Questions

Labetalolo S.A.L.F. contains labetalol, an intravenous beta blocker that is used to treat high blood pressure, including severe hypertensive emergencies, and to relieve angina pectoris by lowering cardiac workload.

Labetalol blocks both alpha‑1 and non‑selective beta‑adrenergic receptors. This dual action causes vasodilation and reduces heart rate and contractility, which together lower peripheral vascular resistance and cardiac output, resulting in decreased arterial pressure.

The dosage of Labetalolo S.A.L.F. is determined by the prescribing clinician based on the patient’s condition, severity of hypertension, and response to therapy. Specific dosing regimens are not provided here.

Safety of labetalol in pregnancy or while breastfeeding has not been definitively established. Healthcare providers should weigh potential benefits against risks and consider alternative treatments when appropriate.

To order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Labetalol’s combined alpha‑ and beta‑blocking profile offers rapid blood‑pressure reduction, which can be advantageous over pure beta‑blockers or vasodilators in acute settings. Compared with nitroprusside, labetalol has a longer duration of action and does not require continuous infusion for the same effect.

Store the product below 25 °C in its original container, protecting it from light and moisture. Do not freeze. Follow standard aseptic handling procedures for intravenous solutions to maintain sterility.

Labetalolo S.A.L.F. is given by intravenous infusion. The prescriber determines the infusion rate and total dose based on the patient’s blood‑pressure targets and clinical response. Administration should be performed by qualified healthcare personnel in a monitored setting.

Serious risks include severe hypotension, bronchospasm in patients with reactive airway disease, hepatic dysfunction, cardiac conduction abnormalities such as heart block, and rare severe skin reactions like Stevens‑Johnson syndrome. Immediate medical attention is required if these occur.

Contraindications include patients with known hypersensitivity to labetalol, severe bradycardia, advanced heart block, uncontrolled asthma or chronic obstructive pulmonary disease, and those with severe hepatic impairment. Clinicians should evaluate each patient’s medical history before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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