Product image of Metoprolol 1 A Pharma (Metoprolol Tartrate Ph. Eur.) supplied by GNH India

Metoprolol 1 A Pharma

Active Ingredient:
Metoprolol Tartrate Ph. Eur.
Origin:
EU

Metoprolol 1 A Pharma (Metoprolol Tartrate Ph. Eur.)

Metoprolol tartrate, the active ingredient in Metoprolol 1 A Pharma, is a beta blocker presented as an oral tablet for oral use. It is employed to lower blood pressure, relieve angina and improve outcomes in heart failure and post‑myocardial infarction patients.
GNH India supplies Metoprolol 1 A Pharma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

1 A Pharma Gmbh

1
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Indications & Clinical Uses

Metoprolol tartrate is a selective β1‑adrenergic antagonist used in several cardiovascular conditions.

  • Hypertension: reduces systolic and diastolic pressure by decreasing cardiac output.
  • Angina pectoris: lowers myocardial oxygen demand, relieving chest pain.
  • Post‑myocardial infarction: improves survival by limiting arrhythmias and remodeling.
  • Chronic heart failure: enhances ventricular function and reduces hospitalisation.
  • 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, inhibiting catecholamine‑induced stimulation of adenylate cyclase. This reduces intracellular cyclic AMP, leading to decreased heart rate, contractility, and conduction velocity, which together lower cardiac output and myocardial oxygen consumption, ultimately producing antihypertensive and anti‑ischemic effects.

Side Effects

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

Common Side Effects

  • Fatigue: feeling unusually tired or weak.
  • Dizziness or light‑headedness, especially on standing.
  • Cold extremities: reduced peripheral circulation.
  • Bradycardia: slower than normal heart rate.
  • Gastrointestinal upset: nausea, abdominal discomfort.
  • Headache: mild to moderate intensity.

Serious or Rare Side Effects

  • Bronchospasm: difficulty breathing, particularly in asthmatic patients.
  • Severe bradycardia or heart block requiring medical attention.
  • Marked hypotension: sudden drop in blood pressure.
  • Allergic reactions: rash, itching, swelling, or anaphylaxis.
  • Depression or mood changes.
  • Worsening heart failure symptoms.

Precautions & Warnings

Before prescribing Metoprolol tartrate, clinicians should consider several safety measures.

  • Assess cardiovascular status: evaluate heart rate and blood pressure prior to initiation.
  • Monitor for bronchospastic disease: avoid or use with caution in uncontrolled asthma or COPD.
  • Adjust in renal impairment: dose may need modification in reduced kidney function.
  • Caution in diabetes: beta‑blockade can mask hypoglycaemia symptoms.
  • Avoid abrupt discontinuation: taper gradually to prevent rebound tachycardia.
  • Store at ambient temperature: keep below 25°C, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Other AV‑nodal blockers (e.g., verapamil, diltiazem): may cause severe bradycardia.
  • Potent CYP2D6 inhibitors (e.g., quinidine, propafenone): increase plasma metoprolol levels.
  • Insulin or sulfonylureas: beta‑blockade may mask hypoglycaemia signs.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may blunt antihypertensive effect.
  • SSRIs or other antidepressants: can enhance bradycardia risk.
  • Thyroid hormones: may alter heart‑rate response, requiring dose adjustment.

Frequently Asked Questions

Metoprolol 1 A Pharma is prescribed to manage high blood pressure, relieve chest pain from angina, improve outcomes after a heart attack, treat chronic heart failure, and control heart rate in certain cardiac arrhythmias such as atrial fibrillation.

Metoprolol tartrate selectively blocks β1‑adrenergic receptors in the heart, reducing the effects of adrenaline and noradrenaline. This lowers heart rate, contractility, and conduction speed, which together decrease cardiac output and myocardial oxygen demand, helping to control blood pressure and reduce ischemic stress.

The appropriate dose of Metoprolol 1 A Pharma is determined by the prescribing clinician based on the individual’s medical condition, response to therapy, and other factors. Patients should follow the dosage instructions provided by their healthcare professional and not adjust the dose on their own.

Safety data for Metoprolol during pregnancy and lactation are limited. The medication should only be used if the potential benefits justify any potential risk to the fetus or infant, and this decision must be made by a qualified healthcare provider.

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) beta blocker, offering a lower risk of bronchospasm compared with non‑selective agents such as propranolol. It is commonly chosen for patients with respiratory concerns, whereas non‑selective blockers may be preferred when broader β‑receptor coverage is needed.

Metoprolol 1 A Pharma should be stored at ambient temperature, below 25 °C, in its original packaging. Keep the product away from excess moisture, heat, and direct sunlight to maintain stability.

Metoprolol 1 A Pharma is taken orally, usually with or without food, as directed by a healthcare professional. The tablet 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 anaphylaxis. Patients should seek immediate medical attention if they experience symptoms like fainting, severe shortness of breath, or swelling of the face and throat.

Metoprolol 1 A Pharma 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 with uncompensated heart failure or severe asthma/COPD where β‑blockade could worsen airway obstruction.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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