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

Metoprolol Medreg

Active Ingredient:
Metoprolol Tartrate
Origin:
EU

Metoprolol Medreg (Metoprolol Tartrate)

Metoprolol Tartrate, the active ingredient in Metoprolol Medreg, is a beta blocker presented as an oral tablet for oral use. It is employed to lower blood pressure, relieve angina and manage certain cardiac rhythm disorders in adult patients.

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

Manufacturer / TM Owner

Medreg S.R.O.

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Indications & Clinical Uses

Metoprolol Medreg is a selective β1‑adrenergic antagonist used in cardiovascular disease management.

  • Hypertension: lowers systolic and diastolic pressure by reducing cardiac output and renin release.
  • Angina pectoris: decreases myocardial oxygen demand, relieving chest pain during exertion.
  • Myocardial infarction: improves survival by limiting infarct size and preventing recurrent ischemia.
  • Heart failure: enhances left‑ventricular function and reduces hospitalisation risk.
  • Cardiac arrhythmias: controls ventricular rate in atrial fibrillation and other supraventricular tachyarrhythmias.

How It Works

  • Metoprolol Tartrate selectively blocks β1‑adrenergic receptors in cardiac tissue, diminishing sympathetic stimulation. This reduces heart rate, myocardial contractility, and renin‑angiotensin activation, leading to lower cardiac output and blood pressure while decreasing myocardial oxygen consumption.

Side Effects

Metoprolol Medreg may cause a range of adverse reactions.

Common Side Effects

  • Fatigue or general weakness
  • Dizziness or light‑headedness
  • Bradycardia (slow heart rate)
  • Cold extremities
  • Gastrointestinal discomfort such as nausea
  • Headache

Serious or Rare Side Effects

  • Severe bradycardia or heart block
  • Marked hypotension
  • Bronchospasm, especially in patients with asthma
  • Allergic reactions including rash or angioedema
  • Depression or mood changes
  • Worsening heart failure symptoms

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety measures.

  • Monitor blood pressure: check regularly to avoid excessive hypotension.
  • Assess heart rate: ensure rate remains within safe limits, especially in patients with conduction disease.
  • Use caution in asthma or chronic obstructive pulmonary disease: β1 selectivity may not fully prevent bronchospasm.
  • Adjust dose in renal impairment: reduced clearance may increase drug exposure.
  • Avoid abrupt discontinuation: taper gradually to prevent rebound tachycardia or hypertension.
  • Store at room temperature: keep in the original pack, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Verapamil or diltiazem: additive negative‑chronotropic effect may cause severe bradycardia.
  • Class IA or III anti‑arrhythmics (e.g., quinidine, amiodarone): risk of profound conduction disturbances.
  • Clonidine abrupt withdrawal: may precipitate hypertensive crisis when combined.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: may enhance hypotensive response.
  • Diuretics: combined effect on blood pressure and electrolyte balance.
  • NSAIDs: can blunt antihypertensive effect.
  • Antidiabetic agents: may mask hypoglycaemia symptoms.
  • CYP2D6 inhibitors (e.g., fluoxetine, paroxetine): increase metoprolol plasma levels.

Frequently Asked Questions

Metoprolol Medreg is prescribed to manage high blood pressure, relieve chest pain from angina, treat heart failure, reduce the risk of complications after a myocardial infarction, and control heart rate in certain cardiac arrhythmias such as atrial fibrillation.

Metoprolol Tartrate selectively blocks β1‑adrenergic receptors in the heart, which diminishes the effects of adrenaline and noradrenaline. This leads to a slower heart rate, reduced force of contraction, and lower renin release, collectively lowering blood pressure and myocardial oxygen demand.

The appropriate dose of Metoprolol Medreg is determined by the prescribing clinician based on the individual’s medical condition, response to therapy, and any co‑existing health issues. Patients should follow the dosage instructions provided by their healthcare professional.

Metoprolol Tartrate is classified as Pregnancy Category B, indicating that animal studies have not shown risk to the fetus, but adequate human data are lacking. It should only be used during pregnancy or lactation if clearly needed and after a risk‑benefit assessment by the prescriber.

To request Metoprolol Medreg, 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 Medreg is a β1‑selective blocker, offering cardiac‑focused effects with less impact on bronchial β2 receptors compared with non‑selective agents like propranolol. This selectivity can make it preferable for patients with respiratory conditions, while still providing effective blood‑pressure and anti‑anginal control.

Metoprolol Medreg should be stored at room temperature, below 25 °C. Keep the tablets in their original packaging, protect them from moisture and direct sunlight, and ensure the container is tightly closed to maintain product stability.

Metoprolol Medreg is taken orally, usually with or without food, as directed by the prescriber. The tablets should be swallowed whole with a glass of water and not chewed or crushed unless specifically instructed.

Serious risks include severe bradycardia, heart block, marked hypotension, bronchospasm in susceptible individuals, and rare allergic reactions such as angioedema. Patients should seek immediate medical attention if they experience fainting, severe shortness of breath, or signs of an allergic response.

Metoprolol Medreg is contraindicated in patients with known hypersensitivity to metoprolol or any component of the formulation, those with severe bradycardia, second‑ or third‑degree heart block without a pacemaker, and individuals experiencing cardiogenic shock or overt heart failure decompensation.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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