Product image of Metoprolol Hexal Z (Metoprolol Succinate) supplied by GNH India

Metoprolol Hexal Z

Active Ingredient:
Metoprolol Succinate
Origin:
EU

Metoprolol Hexal Z (Metoprolol Succinate)

Metoprolol succinate, the active ingredient in Metoprolol Hexal Z, is a beta blocker presented as an oral tablet for oral use. It is prescribed to lower blood pressure, relieve angina and improve outcomes in chronic heart failure and after myocardial infarction.

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

Manufacturer / TM Owner

Hexal Ag

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Indications & Clinical Uses

Metoprolol Hexal Z is a beta‑adrenergic blocker used in several cardiovascular conditions.

  • Hypertension: reduces systolic and diastolic pressure by decreasing cardiac output.
  • Angina pectoris: lowers myocardial oxygen demand, relieving chest pain during exertion.
  • Chronic heart failure: improves survival and reduces hospitalisation by moderating heart rate and contractility.
  • Post‑myocardial infarction prophylaxis: decreases the risk of recurrent cardiac events through heart‑rate control.

How It Works

  • Metoprolol succinate selectively antagonises β1‑adrenergic receptors in cardiac tissue, inhibiting the effects of endogenous catecholamines. This blockade reduces heart rate, myocardial contractility, and conduction velocity, leading to lower cardiac output and decreased arterial pressure, while also diminishing myocardial oxygen consumption.

Side Effects

Metoprolol Hexal Z may cause a range of adverse reactions, most of which are dose‑related and reversible upon discontinuation.

Common Side Effects

  • Fatigue or tiredness
  • Dizziness or light‑headedness
  • Cold extremities
  • Gastrointestinal upset (nausea, abdominal discomfort)
  • Sleep disturbances (insomnia or vivid dreams)

Serious or Rare Side Effects

  • Bradycardia (excessively slow heart rate)
  • Hypotension (significant blood‑pressure drop)
  • Heart block or atrioventricular conduction abnormalities
  • Worsening of heart failure symptoms
  • Severe bronchospasm in patients with underlying airway disease

Precautions & Warnings

Before initiating therapy, clinicians should assess individual risk factors and monitor patients regularly.

  • Cardiovascular assessment: evaluate baseline heart rate, blood pressure and cardiac function.
  • Respiratory status: avoid in patients with uncontrolled asthma or severe chronic obstructive pulmonary disease.
  • Diabetes monitoring: watch for masking of hypoglycaemia symptoms.
  • Concomitant medications: review for potential additive bradycardic or hypotensive agents.
  • Renal/hepatic impairment: adjust dosing or monitor closely in reduced organ function.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Metoprolol Hexal Z can interact with several drug classes, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Non‑selective β‑blockers or other cardio‑depressant agents (risk of profound bradycardia).
  • Calcium channel blockers such as verapamil or diltiazem (enhanced AV‑node blockade).
  • Potent CYP2D6 inhibitors (e.g., quinidine, paroxetine) leading to increased metoprolol exposure.

Moderate Interactions (Monitor Closely)

  • Antidiabetic drugs (may mask hypoglycaemia symptoms).
  • NSAIDs (potential reduction of antihypertensive effect).
  • Antidepressants with serotonergic activity (possible additive dizziness).

Frequently Asked Questions

Metoprolol Hexal Z contains metoprolol succinate, a selective β1‑adrenergic blocker indicated for the management of hypertension, angina pectoris, chronic heart failure, and for secondary prevention after a myocardial infarction. It works by lowering heart rate and cardiac output, which helps control blood pressure and reduces the heart’s oxygen demand.

Metoprolol succinate selectively blocks β1‑adrenergic receptors in the heart, preventing catecholamines such as adrenaline from increasing heart rate and contractility. This results in a slower pulse, reduced myocardial contractile force, and lower cardiac output, thereby decreasing arterial pressure and myocardial oxygen consumption.

The appropriate dose of Metoprolol Hexal Z is determined by the prescribing clinician based on the individual’s medical condition, response to therapy, and any co‑existing health issues. Dosage adjustments are made during follow‑up visits to achieve the desired therapeutic effect while minimising adverse reactions.

The safety of metoprolol succinate in pregnancy and lactation has not been definitively established. It should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and this 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 of Metoprolol Hexal Z. 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 succinate is a cardio‑selective β1‑blocker, offering a favourable side‑effect profile compared with non‑selective agents that also block β2 receptors. Its extended‑release formulation provides once‑daily dosing, which can improve adherence relative to short‑acting beta blockers that require multiple daily doses.

Metoprolol Hexal Z should be stored at ambient temperature, preferably below 25 °C. Keep the tablets in the original container, protect them from moisture and direct sunlight, and ensure the packaging remains tightly closed until use.

Metoprolol Hexal Z is taken orally, usually as a whole tablet with or without food. The extended‑release formulation allows for once‑daily dosing, but patients should follow the prescriber’s instructions regarding timing and whether to take it with meals.

Serious adverse events may include marked bradycardia, severe hypotension, heart block, and worsening of heart‑failure symptoms. Patients should be monitored for signs of these conditions, especially during dose initiation or when combined with other cardiac‑depressant drugs.

Metoprolol Hexal Z is contraindicated in patients with known hypersensitivity to metoprolol or any component of the formulation, those with severe bradycardia, second‑ or third‑degree atrioventricular 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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