Product image of Metoprolol 50mg (Metoprolol Tartrate) supplied by GNH India

Metoprolol 50mg

Active Ingredient:
Metoprolol Tartrate
Origin:
EU

Metoprolol 50mg (Metoprolol Tartrate)

Metoprolol Tartrate, the active ingredient in Metoprolol 50mg, is a beta blocker presented as a 50 mg oral dosage form for oral use. It is employed to lower blood pressure, relieve angina and control heart rate in various cardiac conditions.

GNH India supplies Metoprolol 50mg as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Magistra C&c

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Indications & Clinical Uses

Metoprolol acts on the cardiovascular system to reduce heart rate and myocardial oxygen demand, making it useful for several heart‑related conditions.

  • Hypertension: lowers blood pressure by decreasing cardiac output and renin release.
  • Angina pectoris: reduces chest pain by limiting heart work and oxygen consumption.
  • Post‑myocardial infarction: helps prevent recurrent events by stabilising heart rhythm and reducing workload.
  • Chronic heart failure: improves survival by decreasing sympathetic stimulation and ventricular stress.
  • Arrhythmias (e.g., atrial fibrillation): slows ventricular response through β1‑receptor blockade.

How It Works

  • Metoprolol selectively antagonises β1‑adrenergic receptors in cardiac tissue, which diminishes cyclic AMP formation, leading to reduced intracellular calcium. This results in decreased heart rate, contractility, and renin secretion, thereby lowering blood pressure and myocardial oxygen demand.

Side Effects

Metoprolol may cause a range of adverse reactions, from mild to severe. Patients should be aware of both common and less frequent side effects.

Common Side Effects

  • Fatigue or tiredness.
  • Dizziness or light‑headedness.
  • Bradycardia (slow heart rate).
  • Cold extremities or peripheral vasoconstriction.
  • Gastrointestinal upset such as nausea.
  • Sleep disturbances or vivid dreams.

Serious or Rare Side Effects

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

Precautions & Warnings

Before initiating Metoprolol, clinicians should evaluate patient history and monitor key parameters.

  • Cardiovascular assessment: confirm stable heart rate and blood pressure.
  • Monitor heart rate and blood pressure regularly during therapy.
  • Use caution in patients with asthma or chronic obstructive pulmonary disease.
  • Avoid abrupt discontinuation to prevent rebound hypertension.
  • Adjust dose in renal or hepatic impairment as needed.
  • Store at ambient temperature: keep in the original container, protect from moisture.

Avoid Interactions

Metoprolol can interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • Concomitant use with non‑selective beta blockers may cause excessive β‑blockade.
  • Combined with calcium‑channel blockers such as verapamil or diltiazem can lead to severe bradycardia.
  • Potent CYP2D6 inhibitors (e.g., paroxetine, fluoxetine) increase metoprolol plasma levels.
  • Co‑administration with clonidine may precipitate hypertension on withdrawal.

Moderate Interactions (Monitor Closely)

  • Diuretics may enhance the hypotensive effect of metoprolol.
  • NSAIDs can attenuate its antihypertensive efficacy.
  • Insulin or oral hypoglycemics may mask hypoglycaemia symptoms.

Frequently Asked Questions

Metoprolol 50mg is prescribed to manage high blood pressure, relieve chest pain from angina, reduce the risk of further heart attacks after a myocardial infarction, improve symptoms of chronic heart failure, and control heart rate in certain arrhythmias such as atrial fibrillation.

Metoprolol Tartrate selectively blocks β1‑adrenergic receptors in the heart, which lowers cyclic AMP levels, reduces calcium influx, and consequently decreases heart rate, contractile force, and renin release. This combined effect lowers blood pressure and myocardial oxygen demand.

The exact dose of Metoprolol 50mg is determined by the prescribing clinician based on the individual’s medical condition, response to therapy, and other factors. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for Metoprolol in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the 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 like propranolol. Its once‑daily dosing and proven efficacy in heart failure and post‑MI settings make it a common choice, though individual response and comorbidities guide the final selection.

Metoprolol 50mg tablets should be stored at ambient temperature, below 25 °C, in the original packaging to protect them from moisture and light. Keep the product out of reach of children.

Metoprolol 50mg is taken orally, usually with or without food, as directed by the prescriber. The tablet should be swallowed whole with a glass of water and not chewed or crushed unless specifically advised.

Serious risks include severe bradycardia, marked hypotension, heart block, bronchospasm in patients with reactive airway disease, and rare allergic reactions. Patients should seek immediate medical attention if they experience fainting, extreme fatigue, difficulty breathing, or swelling of the face or throat.

Metoprolol 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 cardiogenic shock.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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