Product image of Metoprololsuccinat Dura (Metoprolol Tartrate) supplied by GNH India

Metoprololsuccinat Dura

Active Ingredient:
Metoprolol Tartrate
Origin:
EU

Metoprololsuccinat Dura (Metoprolol Tartrate)

Metoprolol, the active ingredient in Metoprololsuccinat Dura, is a beta blocker presented as an oral tablet for oral use. It treats hypertension, angina pectoris, heart failure and certain cardiac arrhythmias in adult patients.

GNH India supplies Metoprololsuccinat Dura as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Mylan Germany Gmbh

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Indications & Clinical Uses

Metoprololsuccinat Dura is a beta‑adrenergic blocker used in cardiovascular disease management.

  • Hypertension: lowers systemic blood pressure by reducing cardiac output and inhibiting renin release.
  • Angina pectoris: decreases myocardial oxygen demand through heart‑rate and contractility reduction.
  • Heart failure: improves survival and symptoms by attenuating sympathetic overactivity.
  • Cardiac arrhythmias: controls ventricular rate in atrial fibrillation and other supraventricular tachyarrhythmias.

How It Works

  • Metoprolol selectively antagonizes β1‑adrenergic receptors in cardiac tissue, blocking the effects of endogenous catecholamines. This reduces heart rate, myocardial contractility, and conduction velocity, leading to decreased cardiac output and lower blood pressure. The drug also diminishes renin secretion from the kidneys, contributing to its antihypertensive effect.

Side Effects

Metoprolol may cause a range of adverse reactions, from mild to serious.

Common Side Effects

  • Fatigue or tiredness
  • Dizziness or light‑headedness
  • Cold extremities
  • Gastrointestinal upset (nausea, abdominal discomfort)
  • Sleep disturbances or vivid dreams

Serious or Rare Side Effects

  • Bradycardia or severe heart block
  • Hypotension with syncope
  • Worsening heart failure
  • Bronchospasm in patients with asthma
  • Severe allergic reactions (rash, angioedema)

Precautions & Warnings

Before initiating therapy, consider patient‑specific factors and monitor for adverse events.

  • Cardiovascular assessment: evaluate baseline heart rate, blood pressure, and cardiac function.
  • Respiratory status: avoid in uncontrolled asthma or severe chronic obstructive pulmonary disease.
  • Diabetes monitoring: watch for masking of hypoglycaemic symptoms.
  • Concomitant depression: monitor for worsening mood or suicidal thoughts.
  • Pregnancy and lactation: use only if potential benefit justifies potential risk.
  • Store at below 25°C: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Metoprolol may interact with several drug classes, altering its efficacy or safety.

Major Interactions (Avoid)

  • Non‑selective beta‑blockers: additive bradycardia and hypotension.
  • Calcium channel blockers (verapamil, diltiazem): profound AV‑node depression.
  • Strong CYP2D6 inhibitors (paroxetine, fluoxetine): increased metoprolol plasma levels.

Moderate Interactions (Monitor Closely)

  • Antidiabetic agents: potential masking of hypoglycaemia.
  • NSAIDs: may reduce antihypertensive effect.
  • Diuretics: risk of orthostatic hypotension.
  • Antidepressants (tricyclics): enhanced cardiac conduction effects.

Frequently Asked Questions

Metoprololsuccinat Dura contains metoprolol, a selective β1‑adrenergic blocker indicated for hypertension, angina pectoris, chronic heart failure, and certain cardiac arrhythmias such as atrial fibrillation. It helps control blood pressure, reduce chest pain, improve heart‑failure symptoms, and manage heart‑rate in arrhythmic conditions.

Metoprolol selectively blocks β1‑adrenergic receptors in the heart, preventing catecholamines like adrenaline from increasing heart rate and contractility. This leads to reduced cardiac output, lower blood pressure, and decreased myocardial oxygen demand. It also diminishes renin release from the kidneys, contributing to its antihypertensive effect.

The appropriate dose of Metoprololsuccinat Dura is individualized by a qualified prescriber based on the patient’s clinical condition, response, and tolerability. Dosage may be adjusted over time, and patients should follow the prescribing physician’s instructions without self‑adjusting the amount.

Safety data for metoprolol in pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant. Healthcare providers will assess each case and discuss alternatives if appropriate.

To place an 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 (including any cold‑chain requirements), and necessary import documentation.

Metoprolol is a cardio‑selective β1‑blocker, offering a lower risk of bronchospasm compared with non‑selective agents such as propranolol. Its pharmacokinetic profile provides once‑ or twice‑daily dosing, and it is widely used for heart‑failure management, whereas some beta blockers are preferred for migraine prophylaxis or tremor control.

Store Metoprololsuccinat Dura at temperatures below 25 °C in a dry place. Keep the product in its original packaging, protect it from moisture, heat, and direct sunlight, and ensure the container is tightly closed when not in use.

Metoprololsuccinat Dura is taken orally, usually with or without food, as directed by the prescribing clinician. Tablets should be swallowed whole with a glass of water and not chewed or crushed unless specifically instructed.

Serious adverse events may include severe bradycardia, symptomatic hypotension, worsening heart failure, bronchospasm in patients with reactive airway disease, and rare allergic reactions such as angioedema. Patients should seek immediate medical attention if they experience fainting, chest pain, difficulty breathing, or swelling of the face or throat.

Metoprololsuccinat Dura is contraindicated in patients with known hypersensitivity to metoprolol or any component of the formulation, those with severe bradycardia, second‑ or third‑degree atrioventricular block without a pacemaker, cardiogenic shock, or overt decompensated heart failure. Caution is also advised for individuals with uncontrolled asthma or severe peripheral vascular disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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