Product image of Labetalol Stragen (Labetalol Hydrochloride) supplied by GNH India

Labetalol Stragen

Active Ingredient:
Labetalol Hydrochloride
Origin:
EU

Labetalol Stragen (Labetalol Hydrochloride)

Labetalol, the active ingredient in Labetalol Stragen, is a alpha/beta adrenergic blocker presented as an intravenous formulation for intravenous use. It treats hypertension and hypertensive emergencies in adult patients.
GNH India supplies Labetalol Stragen 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 to manage conditions related to elevated blood pressure and vascular resistance.
  • Hypertension: lowers systemic blood pressure by reducing cardiac output and peripheral vascular resistance.
  • Hypertensive emergencies: provides rapid blood pressure control in acute, life‑threatening situations.
  • Acute severe hypertension: stabilises patients with sudden, marked elevations in arterial pressure.

How It Works

  • Labetalol acts as a non‑selective β‑adrenergic antagonist while also blocking α1‑adrenergic receptors. The combined β‑blockade reduces heart rate and myocardial contractility, decreasing cardiac output, whereas α1‑blockade causes vasodilation, lowering peripheral vascular resistance. Together these actions result in a net reduction of arterial blood pressure.

Side Effects

Common Side Effects

  • Dizziness or light‑headedness
  • Headache
  • Nausea or vomiting
  • Fatigue or weakness
  • Flushing or warmth sensation
  • Tachycardia or palpitations

Serious or Rare Side Effects

  • Severe hypotension leading to syncope
  • Bronchospasm, especially in patients with asthma
  • Hepatic dysfunction or elevated liver enzymes
  • Heart block or severe bradyarrhythmias
  • Anaphylactic or severe allergic reactions
  • Acute heart failure or pulmonary edema

Precautions & Warnings

Labetalol should be used with clinical monitoring and awareness of specific safety considerations.

  • Blood pressure monitoring: check frequently during initiation and dose adjustments.
  • Asthma or chronic obstructive pulmonary disease: use cautiously due to potential bronchospasm.
  • Abrupt discontinuation: avoid sudden stop to prevent rebound hypertension.
  • Hepatic impairment: consider dose reduction and monitor liver function.
  • Diabetes: monitor blood glucose as β‑blockade may mask hypoglycaemia symptoms.
  • Store at room temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Labetalol may interact with several drug classes that affect cardiovascular function.

Major Interactions (Avoid)

  • Other antihypertensives (e.g., additional β‑blockers, ACE inhibitors) – risk of excessive hypotension.
  • Calcium channel blockers such as verapamil – additive negative inotropic effect.
  • Monoamine oxidase inhibitors – potential for severe hypertension.
  • Clonidine – abrupt withdrawal may cause rebound hypertension.
  • Epinephrine or other sympathomimetics – antagonistic effect reducing therapeutic response.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs – may blunt antihypertensive effect.
  • Diuretics – monitor electrolytes and blood pressure.
  • Antidepressants (SSRIs, SNRIs) – possible additive central nervous system effects.
  • Anesthetic agents – may enhance cardiovascular depression.
  • Antiarrhythmic drugs – monitor cardiac rhythm for bradyarrhythmias.

Frequently Asked Questions

Labetalol Stragen is an intravenous antihypertensive medication used to lower high blood pressure and to provide rapid blood pressure control in hypertensive emergencies. It is indicated for adult patients who require swift and controlled reduction of arterial pressure.

Labetalol blocks both β‑adrenergic receptors, reducing heart rate and contractility, and α1‑adrenergic receptors, causing vasodilation. The combined effect decreases cardiac output and peripheral vascular resistance, leading to a net reduction in systemic blood pressure.

The dosing regimen for Labetalol Stragen is determined by the prescribing clinician based on the patient’s clinical condition, severity of hypertension, and response to therapy. Dosage is individualized and administered intravenously under medical supervision.

Safety data for Labetalol Stragen in pregnancy or lactation are limited. Use during pregnancy or while breastfeeding should only be considered if the potential benefit justifies the potential risk to the fetus or infant, and it must be decided by the treating physician.

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

Labetalol is unique because it combines β‑blockade with α1‑blockade, offering both reduced cardiac output and vasodilation. Compared with selective β‑blockers, it may provide better control of peripheral resistance, while compared with pure α‑blockers, it also limits heart rate increases.

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

Labetalol Stragen is administered intravenously by a qualified healthcare professional. The infusion rate and total dose are adjusted according to the patient’s blood pressure response and clinical monitoring during treatment.

Serious risks include severe hypotension, bronchospasm in patients with reactive airway disease, hepatic dysfunction, heart block or severe bradyarrhythmias, and rare anaphylactic reactions. Prompt medical attention is required if any of these events occur.

Labetalol Stragen is contraindicated in patients with known hypersensitivity to labetalol or any component of the formulation, severe bradycardia, advanced heart block without a pacemaker, and in patients with uncontrolled asthma or severe chronic obstructive pulmonary disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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