Product image of Metocard (Metoprolol Tartrate) supplied by GNH India

Metocard

Active Ingredient:
Metoprolol Tartrate
Origin:
EU

Metocard (Metoprolol Tartrate)

Metoprolol tartrate, the active ingredient in Metocard, is a selective β1‑adrenergic receptor blocker presented as an oral tablet for systemic use. It is indicated for the management of hypertension, angina pectoris, chronic heart failure, and post‑myocardial infarction in adult patients.

GNH India supplies Metocard as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The product conforms to EU quality standards and is manufactured under GMP conditions.

Manufacturer / TM Owner

Zaklady Farmaceutyczne Polpharma S.A.

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Indications & Clinical Uses

  • Metocard (metoprolol tartrate) is a beta‑blocker used to manage cardiovascular conditions that involve elevated blood pressure or cardiac workload.
  • Hypertension: lowers systolic and diastolic blood pressure.
  • Angina pectoris: reduces myocardial oxygen demand and relieves chest pain.
  • Heart failure: improves left‑ventricular function and reduces hospitalisation risk.
  • Post‑myocardial infarction: decreases the likelihood of recurrent infarction and mortality.

How It Works

  • Metoprolol tartrate selectively antagonises β1‑adrenergic receptors in cardiac tissue, leading to a reduction in heart rate, myocardial contractility, and cardiac output. The drug also diminishes renin release from the kidneys, contributing to lower systemic vascular resistance and blood pressure.

Side Effects

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

Common Side Effects

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

Serious or Rare Side Effects

  • Severe bradycardia or heart block
  • Marked hypotension
  • Bronchospasm, especially in patients with asthma or COPD
  • Acute decompensated heart failure
  • Depression or mood changes
  • Allergic reactions such as rash, angio‑edema, or anaphylaxis

Precautions & Warnings

  • When prescribing Metocard, clinicians should consider several safety measures.
  • Dose adjustment in renal impairment: reduce dose as needed.
  • Monitor heart rate and blood pressure: check regularly during therapy.
  • Avoid abrupt discontinuation: taper to prevent rebound hypertension.
  • Caution in asthma or COPD: may provoke bronchospasm.
  • Pregnancy and lactation: use only if benefits outweigh risks.
  • Store at ambient temperature: keep below 25 °C, retain original packaging, protect from moisture.

Avoid Interactions

Metocard can interact with other medicines, requiring attention to avoid harmful effects.

Major Interactions (Avoid)

  • Concomitant use with non‑selective beta‑blockers: additive bradycardia.
  • Combination with calcium‑channel blockers (verapamil, diltiazem): risk of severe AV block.
  • Co‑administration with potent CYP2D6 inhibitors (e.g., quinidine, paroxetine): may increase plasma levels.
  • Concurrent clonidine withdrawal: precipitates hypertensive crisis.

Moderate Interactions (Monitor Closely)

  • Co‑administration with diuretics: may enhance hypotensive effect.
  • Use with insulin or oral hypoglycemics: may mask hypoglycaemia symptoms.
  • Concurrent NSAIDs: may reduce antihypertensive efficacy.

Frequently Asked Questions

Metocard contains metoprolol tartrate, a beta‑blocker that is prescribed for hypertension, angina pectoris, chronic heart failure, and for secondary prevention after a myocardial infarction. These indications target conditions where reducing heart rate and cardiac workload improves outcomes.

Metoprolol tartrate selectively blocks β1‑adrenergic receptors in the heart, which slows the heart rate, decreases contractile force, and lowers cardiac output. It also reduces renin secretion from the kidneys, helping to lower systemic blood pressure.

The dose of Metocard is individualized by the prescribing clinician based on the patient’s condition, response, and tolerability. Dosage may be started low and titrated upward, but exact amounts should follow the prescriber’s instructions.

The safety of Metocard in pregnancy and lactation has not been definitively established. It should only be used if the potential benefit justifies any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To request Metocard, 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.

Metocard (metoprolol tartrate) is a cardio‑selective β1‑blocker, offering a favorable profile for patients with respiratory disease compared with non‑selective agents. Compared with extended‑release metoprolol succinate, the tartrate form is typically dosed multiple times daily and may be preferred for certain acute indications.

Metocard tablets should be stored at ambient temperature, below 25 °C, in their original container to protect from moisture and light. Keep the product out of reach of children and do not use after the expiry date printed on the label.

Metocard is taken orally, usually with a glass of water. It can be taken with or without food, but patients should follow the prescriber’s guidance on timing relative to meals to ensure consistent absorption.

Serious risks include severe bradycardia, heart block, marked hypotension, bronchospasm in susceptible individuals, and acute decompensated heart failure. Patients should seek immediate medical attention if they experience fainting, severe dizziness, shortness of breath, or chest pain.

Metocard is contraindicated in patients with known hypersensitivity to metoprolol or other beta‑blockers, those with severe bradycardia, second‑ or third‑degree AV block without a pacemaker, cardiogenic shock, and uncontrolled asthma or severe chronic obstructive pulmonary disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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