Product image of Metoprolol Retard 1a Farma (Metoprolol Tartrate) supplied by GNH India

Metoprolol Retard 1a Farma

Active Ingredient:
Metoprolol Tartrate
Origin:
EU

Metoprolol Retard 1a Farma (Metoprolol Tartrate)

Metoprolol Tartrate, the active ingredient in Metoprolol Retard 1a Farma, is a beta‑adrenergic blocker presented as a tablet for oral use. It is used to manage high blood pressure, relieve angina, and improve outcomes in heart failure and post‑myocardial infarction patients.

GNH India supplies Metoprolol Retard 1a Farma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

1a Farma A/S

1
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Indications & Clinical Uses

Metoprolol Tartrate is employed in cardiovascular therapy to control blood pressure and reduce cardiac workload.

  • Hypertension: lowers systolic and diastolic pressure, decreasing the risk of stroke and organ damage.
  • Angina pectoris: reduces myocardial oxygen demand, alleviating chest pain during exertion.
  • Chronic heart failure: improves ventricular function and reduces hospitalisation rates.
  • Post‑myocardial infarction prophylaxis: decreases the likelihood of recurrent cardiac events and mortality.

How It Works

  • Metoprolol Tartrate selectively blocks β1‑adrenergic receptors in cardiac tissue, leading to a reduction in heart rate, myocardial contractility, and renin release. This combined effect diminishes cardiac output and systemic vascular resistance, thereby lowering arterial blood pressure and myocardial oxygen consumption.

Side Effects

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

Common Side Effects

  • Fatigue or tiredness
  • Dizziness, especially on standing
  • Cold extremities or reduced peripheral circulation
  • Gastrointestinal upset such as nausea or abdominal discomfort
  • Mild bradycardia (slow heart rate)
  • Sleep disturbances or vivid dreams

Serious or Rare Side Effects

  • Severe bradycardia or heart block
  • Acute heart failure exacerbation
  • Bronchospasm in patients with asthma or COPD
  • Hypotensive crisis with syncope
  • Depression or mood changes
  • Allergic reactions including rash, angioedema, or anaphylaxis

Precautions & Warnings

Before initiating therapy, clinicians should assess individual risk factors and monitor patients regularly.

  • Cardiovascular assessment: evaluate baseline heart rate, blood pressure, and cardiac function.
  • Respiratory conditions: avoid in uncontrolled asthma or severe chronic obstructive pulmonary disease.
  • Diabetes management: monitor blood glucose as β‑blockers may mask hypoglycaemia symptoms.
  • Concomitant drugs: review for potential interactions, especially with other rate‑controlling agents.
  • Pregnancy and lactation: use only if clearly needed after risk‑benefit evaluation.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Metoprolol Tartrate can influence, and be influenced by, several co‑administered medicines.

Major Interactions (Avoid)

  • Non‑selective β‑blockers: additive bradycardia and hypotension.
  • Calcium channel blockers (verapamil, diltiazem): profound AV‑node suppression.
  • Antidiabetic agents: may mask hypoglycaemia signs.

Moderate Interactions (Monitor Closely)

  • CYP2D6 inhibitors (e.g., fluoxetine, quinidine): increase metoprolol plasma levels.
  • NSAIDs: may reduce antihypertensive efficacy.
  • Antidepressants (tricyclics, MAO‑inhibitors): potential for enhanced cardiac depression.

Frequently Asked Questions

Metoprolol Retard 1a Farma is prescribed to treat hypertension, angina pectoris, chronic heart failure, and to reduce the risk of recurrent events after a myocardial infarction. It works by lowering heart rate and blood pressure, thereby decreasing the heart’s workload.

Metoprolol Tartrate selectively blocks β1‑adrenergic receptors in the heart. This action slows the heart rate, reduces the force of contraction, and limits the release of renin, leading to lower blood pressure and reduced oxygen demand by the myocardium.

The appropriate dose of Metoprolol Retard 1a Farma is determined by the prescribing clinician based on the patient’s medical condition, response to therapy, and any concomitant medications. Patients should follow the prescriber’s instructions exactly.

Safety in pregnancy and lactation has not been fully established. The drug should only be used if the potential benefit justifies the possible risk to the fetus or infant, and this decision must be made by a qualified healthcare professional.

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 and any necessary import documentation.

Metoprolol is a cardio‑selective (β1‑selective) blocker, offering a lower risk of bronchospasm compared with non‑selective agents such as propranolol. It is commonly chosen for patients with cardiovascular disease who also have respiratory concerns, though individual response can vary.

Store the tablets at ambient temperature, preferably below 25 °C. Keep them in the original container, protect from moisture and direct sunlight, and ensure they are out of reach of children.

Metoprolol Retard 1a Farma is taken orally, usually with or without food, as directed by the prescriber. Tablets should be swallowed whole with a glass of water and not crushed or chewed.

Serious risks include severe bradycardia, heart block, hypotensive crisis, bronchospasm in susceptible individuals, and worsening heart failure. Patients should seek immediate medical attention if they experience fainting, extreme fatigue, shortness of breath, or chest pain.

Metoprolol should be avoided in patients with known severe bradycardia, second‑ or third‑degree atrioventricular block, uncompensated heart failure, or uncontrolled asthma/COPD. It is also contraindicated in individuals with a known hypersensitivity to metoprolol or any excipients in the formulation.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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