Product image of Metozok (Metoprolol Succinate) supplied by GNH India

Metozok

Active Ingredient:
Metoprolol Succinate
Origin:
EU

Metozok (Metoprolol Succinate)

Metoprolol succinate, the active ingredient in Metozok, is a beta blocker presented as an oral dosage form for oral use. It is indicated for the management of hypertension, angina pectoris, chronic heart failure, and for post‑myocardial infarction prophylaxis in adult patients.

GNH India supplies Metozok as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory documentation for export to multiple regions. Customers benefit from reliable delivery schedules and dedicated technical support.

Manufacturer / TM Owner

Sandoz Pharmaceuticals D.D.

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Indications & Clinical Uses

  • Metozok (metoprolol succinate) is a beta‑blocker used in cardiovascular disease management, particularly conditions involving elevated blood pressure or cardiac workload.
  • Hypertension: lowers systolic and diastolic blood pressure, reducing the risk of stroke and cardiovascular events.
  • Angina pectoris: decreases myocardial oxygen demand, relieving chest pain during exertion.
  • Chronic heart failure: improves ventricular function and reduces hospitalizations by lowering heart rate and cardiac output.
  • Post‑myocardial infarction prophylaxis: reduces the likelihood of recurrent infarction and mortality through long‑term heart rate control.

How It Works

  • Metoprolol succinate selectively blocks β1‑adrenergic receptors in cardiac tissue, inhibiting catecholamine‑induced stimulation of the heart. This antagonism reduces heart rate, myocardial contractility, and conduction velocity, leading to decreased cardiac output and lower arterial pressure. The resulting reduction in myocardial oxygen consumption underlies its anti‑anginal and heart‑failure benefits, and by attenuating sympathetic drive it also contributes to improved ventricular remodeling over time.

Side Effects

Metozok may be associated with a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Fatigue: feeling of tiredness or lack of energy.
  • Dizziness: light‑headed sensation, especially on standing.
  • Gastrointestinal upset: nausea, abdominal discomfort or constipation.

Serious or Rare Side Effects

  • Severe bradycardia: markedly low heart rate requiring medical attention.
  • Hypotension: significant drop in blood pressure causing faintness.
  • Bronchospasm: narrowing of airways, particularly in patients with asthma.

Precautions & Warnings

When prescribing Metozok, clinicians should consider several safety measures to minimize risks.

  • Blood pressure monitoring: check regularly to avoid excessive hypotension.
  • Heart rate assessment: ensure rate remains above safe threshold before dose changes.
  • Respiratory caution: use carefully in patients with asthma or chronic obstructive pulmonary disease.
  • Renal/hepatic function: adjust dose in moderate to severe impairment.
  • Discontinuation guidance: avoid abrupt cessation to prevent rebound hypertension or tachycardia.
  • Store below 25°C: keep in the original packaging, protect from moisture and light.

Avoid Interactions

Metozok can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Verapamil or diltiazem: combined use may cause profound bradycardia or heart block.
  • Clonidine withdrawal: abrupt discontinuation of clonidine while on Metozok can precipitate severe hypertension.
  • Amiodarone: increases plasma concentration of metoprolol, raising risk of adverse effects.

Moderate Interactions (Monitor Closely)

  • Calcium channel blockers (non‑dihydropyridine): may enhance negative chronotropic effect.
  • ACE inhibitors or ARBs: additive blood pressure lowering, monitor for hypotension.

Frequently Asked Questions

Metozok contains metoprolol succinate, a selective β1‑adrenergic blocker indicated for the treatment of hypertension, angina pectoris, chronic heart failure, and for reducing the risk of recurrent myocardial infarction in adult patients.

Metoprolol succinate blocks β1‑adrenergic receptors in the heart, decreasing sympathetic stimulation. This leads to a lower heart rate, reduced contractility, and diminished cardiac output, which together lower blood pressure and myocardial oxygen demand.

The dose of Metozok is individualized by the prescribing clinician based on the specific indication, patient characteristics, and response to therapy. Dosage adjustments are made according to clinical guidelines and tolerability.

Safety data for metoprolol succinate during pregnancy and lactation are limited. It should only be used when the potential benefit justifies the potential risk to the fetus or infant, and decisions are made in consultation with a healthcare professional.

To order Metozok, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and import documentation.

Both Metozok (metoprolol succinate) and atenolol are selective β1‑blockers, but metoprolol has a longer half‑life, allowing once‑daily dosing, and provides more consistent heart‑rate control. Atenolol is less lipophilic, which may affect central nervous system penetration and side‑effect profile.

Metozok should be stored below 25 °C in its original packaging, protected from moisture and direct light. Do not store in a bathroom or near a heat source, and keep out of reach of children.

Metozok is taken orally, usually as a whole tablet swallowed with a glass of water. It may be taken with or without food, but consistency with respect to meals helps maintain stable drug levels.

Serious risks include severe bradycardia, marked hypotension, heart block, bronchospasm in patients with reactive airway disease, and rare allergic reactions such as anaphylaxis. Prompt medical attention is required if any of these events occur.

Metozok is contraindicated in patients with severe bradycardia (heart rate < 45 bpm), second‑ or third‑degree atrioventricular block without a pacemaker, uncontrolled asthma or chronic obstructive pulmonary disease, and in individuals with known hypersensitivity to metoprolol or any excipients.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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