Product image of Metoprolol Tartrate Ipca Laboratories Uk (Metoprolol Tartrate) supplied by GNH India

Metoprolol Tartrate Ipca Laboratories Uk

Active Ingredient:
Metoprolol Tartrate
Origin:
EU

Metoprolol Tartrate Ipca Laboratories Uk (Metoprolol Tartrate)

Metoprolol Tartrate, the active ingredient in Metoprolol Tartrate Ipca Laboratories Uk, is a beta blocker presented as a tablet for oral use. It treats hypertension, angina pectoris, post‑myocardial infarction, heart failure and certain cardiac arrhythmias in adult patients.

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

Manufacturer / TM Owner

Ipca Laboratories Uk Limited

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Indications & Clinical Uses

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

  • Hypertension: lowers blood pressure by reducing heart rate and cardiac output.
  • Angina pectoris: decreases myocardial oxygen demand, relieving chest pain.
  • Post‑myocardial infarction: reduces risk of recurrent infarction and improves survival.
  • Heart failure: improves ventricular function and reduces symptoms.
  • Cardiac arrhythmias: controls heart rate in atrial fibrillation and other supraventricular tachyarrhythmias.

How It Works

  • Metoprolol Tartrate selectively blocks β1‑adrenergic receptors in the heart, inhibiting catecholamine‑induced stimulation. This results in decreased heart rate, reduced myocardial contractility, and lower cardiac output, which together lower arterial 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 or light‑headedness
  • Cold extremities
  • Bradycardia (slow heart rate)
  • Gastrointestinal upset (nausea, abdominal discomfort)
  • Headache

Serious or Rare Side Effects

  • Severe bradycardia or heart block
  • Marked hypotension
  • Bronchospasm, especially in patients with asthma
  • Allergic reactions (rash, angioedema)
  • Depression or mood changes
  • Cardiogenic shock

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor for potential complications.

  • Cardiovascular assessment: avoid in patients with severe bradycardia or advanced heart block.
  • Respiratory conditions: use cautiously in asthma or chronic obstructive pulmonary disease.
  • Diabetes monitoring: may mask hypoglycaemia symptoms; adjust glucose monitoring.
  • Concomitant beta‑blockers: avoid additive negative chronotropic effects.
  • Pregnancy considerations: safety category unknown; prescribe only if benefits outweigh risks.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Metoprolol Tartrate can interact with several drug classes; some combinations should be avoided, while others require close monitoring.

Major Interactions (Avoid)

  • Calcium channel blockers (verapamil, diltiazem): may cause profound bradycardia.
  • CYP2D6 inhibitors (quinidine, propafenone): increase metoprolol plasma levels.
  • Clonidine: abrupt discontinuation after concurrent use can precipitate hypertension.
  • Insulin or oral hypoglycemics: enhanced glucose‑lowering effect.
  • Non‑selective beta blockers: additive negative cardiac effects.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may reduce antihypertensive efficacy.
  • Diuretics: risk of excessive blood pressure reduction.
  • Antidepressants (SSRIs, SNRIs): potential for bradycardia.
  • Antithyroid drugs: may alter heart rate response.
  • Anesthetic agents: increased risk of intra‑operative hypotension.

Frequently Asked Questions

Metoprolol Tartrate is prescribed to manage high blood pressure, relieve angina pectoris, reduce the risk of recurrent heart attacks, treat certain types of heart failure, and control heart rate in atrial fibrillation or other supraventricular arrhythmias.

The drug selectively blocks β1‑adrenergic receptors in cardiac tissue, diminishing the effects of adrenaline and noradrenaline. This leads to a slower heart rate, reduced contractile force, and lower cardiac output, which together lower blood pressure and myocardial oxygen demand.

The exact dose is determined by the prescribing clinician based on the individual’s condition, response, and tolerability. Typical regimens range from low to moderate daily doses, but the prescriber will tailor the schedule to each patient’s needs.

Safety data for Metoprolol Tartrate in pregnancy and lactation are limited. It should only be used when the potential benefit justifies any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

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 Tartrate is a selective β1‑blocker, offering cardiac‑focused effects with fewer respiratory side effects than non‑selective agents like propranolol. Compared with atenolol, it has a shorter half‑life, which may require multiple daily dosing, but both share similar efficacy for hypertension and angina.

Store the tablets at ambient temperature, ideally below 25 °C, in the original container to protect them from moisture and light. Keep out of reach of children and do not use if the packaging is damaged.

Metoprolol Tartrate is taken orally, usually as a whole tablet with or without food. Swallow the tablet whole with a full glass of water; do not crush, chew, or split unless specifically instructed by a healthcare provider.

Serious adverse events include severe bradycardia, marked hypotension, heart block, bronchospasm in patients with asthma or COPD, and rare allergic reactions such as angioedema. Patients should seek immediate medical attention if they experience fainting, severe shortness of breath, or swelling of the face or throat.

Metoprolol Tartrate is contraindicated in individuals with severe sinus bradycardia, second‑ or third‑degree atrioventricular block, cardiogenic shock, uncontrolled heart failure, and those with a known hypersensitivity to the drug or any excipients. Caution is also advised for patients with severe asthma or chronic obstructive pulmonary disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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