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

Metoprolosuccinat Dura

Active Ingredient:
Metoprolol Tartrate
Origin:
EU

Metoprolosuccinat Dura (Metoprolol Tartrate)

Metoprolol, the active ingredient in Metoprolosuccinat Dura, is a beta blocker presented as an oral tablet for oral use. It selectively blocks β1‑adrenergic receptors, thereby reducing heart rate and myocardial contractility, and is indicated for hypertension, angina pectoris, post‑myocardial infarction care, and chronic heart failure in adult patients.

GNH India supplies Metoprolosuccinat Dura as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring quality and regulatory conformity across global markets.

Manufacturer / TM Owner

Mylan Germany Gmbh

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Indications & Clinical Uses

  • Metoprolol is a selective β1‑adrenergic blocker used in cardiovascular disease management.
  • Hypertension: lowers blood pressure by reducing cardiac output and renin release.
  • Angina pectoris: decreases myocardial oxygen demand, relieving chest pain.
  • Post‑myocardial infarction: improves survival and reduces risk of recurrent events.
  • Chronic heart failure: enhances left ventricular function and reduces hospitalization.

How It Works

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

Side Effects

Metoprolol may be associated with a range of adverse reactions, varying in frequency and severity.

Common Side Effects

  • Fatigue: feeling of tiredness.
  • Dizziness: light‑headedness on standing.
  • Bradycardia: slower heart rate.
  • Gastrointestinal upset: nausea or abdominal discomfort.

Serious or Rare Side Effects

  • Severe bradycardia: heart rate dangerously low.
  • Heart block: impaired cardiac conduction.
  • Hypotension: markedly low blood pressure.
  • Bronchospasm: airway narrowing, especially in asthma.

Precautions & Warnings

When prescribing Metoprolol, clinicians should consider several precautionary measures to ensure safe use.

  • Assess cardiovascular status: evaluate heart rate and blood pressure before initiation.
  • Review respiratory history: avoid in patients with active bronchospastic disease.
  • Monitor for diabetes: may mask hypoglycemia symptoms.
  • Adjust in renal/hepatic impairment: dose may need modification.
  • Caution in elderly: increased sensitivity to hypotension and bradycardia.
  • Store at ambient temperature: keep below 25°C in original packaging, protect from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • Non‑selective beta blockers: additive bradycardia and hypotension.
  • Calcium channel blockers (verapamil, diltiazem): risk of severe bradycardia and AV block.
  • Antidiabetic agents (insulin, sulfonylureas): may enhance hypoglycemia unawareness.

Moderate Interactions (Monitor Closely)

  • Antidepressants (SSRIs, SNRIs): may increase plasma levels of metoprolol.
  • NSAIDs: can reduce antihypertensive effect.
  • Antithyroid drugs: may diminish metoprolol’s heart‑rate control.

Frequently Asked Questions

Metoprolosuccinat Dura contains metoprolol tartrate, a selective β1‑adrenergic blocker indicated for the treatment of hypertension, angina pectoris, post‑myocardial infarction management, and chronic heart failure in adult patients. By lowering heart rate and myocardial contractility, it helps control blood pressure and reduces cardiac workload, contributing to improved cardiovascular outcomes when used as part of a comprehensive treatment plan.

Metoprolol works by selectively binding to β1‑adrenergic receptors in the heart, blocking the effects of adrenaline and noradrenaline. This antagonism reduces heart rate, contractile force, and conduction velocity, leading to lower cardiac output and blood pressure. It also suppresses renin release from the kidneys, further contributing to its antihypertensive action.

The appropriate dose of Metoprolosuccinat Dura is determined by the prescribing clinician based on the individual’s medical condition, response to therapy, and tolerance. Dosage may be started low and titrated upward, and adjustments are often required for renal or hepatic impairment. Patients should follow the exact regimen provided by their healthcare professional.

Safety data for metoprolol in pregnancy are limited, and the drug should only be used if the potential benefit justifies any possible risk to the fetus. It is excreted in breast milk, so caution is advised for nursing mothers, and a healthcare provider should evaluate the risk‑benefit balance before continuation during lactation.

To place an order, visit the product page on gnhindia.com, enter the required quantity, and submit the enquiry form. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifying trade or institutional credentials before providing a formal quotation, confirming availability, shipping terms, and any necessary import documentation.

Metoprolol is a cardio‑selective β1‑blocker, offering a favorable profile for patients with respiratory conditions compared with non‑selective agents like propranolol. Compared with newer agents such as carvedilol, metoprolol has a simpler dosing schedule and fewer vasodilatory effects, but the choice of therapy depends on individual patient characteristics, comorbidities, and physician preference.

Metoprolosuccinat Dura should be stored at ambient temperature, preferably below 25 °C. Keep the tablets in the original container, protect them from moisture and direct sunlight, and ensure the packaging remains tightly closed until use. Do not store in a refrigerator or freezer, as temperature extremes may affect tablet integrity.

The medication is taken orally, usually with or without food, as directed by a healthcare professional. Tablets should be swallowed whole with a glass of water and not chewed or crushed, unless specifically instructed. Consistent timing each day helps maintain stable blood levels, and patients should avoid abrupt discontinuation without medical guidance.

The most serious adverse events include severe bradycardia, heart block, marked hypotension, and bronchospasm, particularly in patients with underlying respiratory disease. These reactions can be life‑threatening and require immediate medical attention. Regular monitoring of heart rate, blood pressure, and respiratory status is essential, especially during dose adjustments or when interacting drugs are introduced.

Metoprolosuccinat Dura is contraindicated in patients with known hypersensitivity to metoprolol or any component of the formulation, those with severe sinus bradycardia, second‑ or third‑degree atrioventricular block without a pacemaker, and individuals experiencing cardiogenic shock. Caution is also advised for patients with uncontrolled asthma or severe chronic obstructive pulmonary disease, as β1‑selectivity may not fully prevent bronchoconstriction.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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