Product image of Metoprolol Succinat Tad (Metoprolol Succinate) supplied by GNH India

Metoprolol Succinat Tad

Active Ingredient:
Metoprolol Succinate
Origin:
EU

Metoprolol Succinat Tad (Metoprolol Succinate)

Metoprolol succinate, the active ingredient in Metoprolol Succinate Tad, is a beta blocker presented as an oral tablet for oral use. It is used to manage high blood pressure, chest pain, heart failure and to improve survival after a heart attack.
GNH India supplies Metoprolol Succinate Tad as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Tad Pharma Gmbh

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Indications & Clinical Uses

Metoprolol succinate is a selective β1‑adrenergic blocker indicated for several cardiovascular conditions.

  • Hypertension: lowers systolic and diastolic blood pressure to reduce cardiovascular risk.
  • Angina pectoris: decreases myocardial oxygen demand, relieving chest pain during exertion.
  • Chronic heart failure: improves left‑ventricular function and reduces hospitalisation rates.
  • Post‑myocardial infarction: lowers the chance of recurrent infarction and improves long‑term survival.

How It Works

  • Metoprolol succinate selectively antagonises β1‑adrenergic receptors in cardiac tissue, inhibiting catecholamine‑induced stimulation of adenylate cyclase. This reduces cyclic AMP formation, leading to decreased heart rate, contractility, and myocardial oxygen consumption, while also lowering peripheral vascular resistance and blood pressure.

Side Effects

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

Common Side Effects

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

Serious or Rare Side Effects

  • Severe bradycardia or heart block requiring medical attention.
  • Marked hypotension leading to fainting.
  • Bronchospasm in patients with reactive airway disease.
  • Depression or mood changes.
  • Allergic reactions such as rash, itching or angioedema.
  • Worsening heart failure symptoms.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate cardiovascular status and consider potential risks.

  • Cardiac assessment: confirm stable heart rhythm and function.
  • Blood pressure monitoring: check regularly during dose titration.
  • Renal function: adjust dose in patients with impaired clearance.
  • Concomitant beta‑blockers: avoid duplicate therapy to prevent excessive blockade.
  • Discontinuation: taper gradually to prevent rebound hypertension or tachycardia.
  • Store at below 25°C: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Metoprolol succinate can interact with several drug classes, influencing its efficacy and safety.

Major Interactions (Avoid)

  • Other beta‑blockers: additive cardiac depression.
  • Calcium‑channel blockers (verapamil, diltiazem): increased risk of AV‑block and bradycardia.
  • Strong CYP2D6 inhibitors (e.g., quinidine, fluoxetine): raise metoprolol plasma levels.

Moderate Interactions (Monitor Closely)

  • Diuretics: may potentiate hypotensive effect.
  • NSAIDs: can blunt antihypertensive response.
  • Antidepressants (SSRIs, SNRIs): monitor for enhanced bradycardia.
  • Antidiabetic agents: mask hypoglycaemia symptoms.
  • ACE inhibitors or ARBs: watch for additive blood‑pressure lowering.

Frequently Asked Questions

Metoprolol Succinate Tad is prescribed to treat hypertension, angina pectoris, chronic heart failure, and to reduce the risk of further cardiac events after a myocardial infarction. It works by lowering heart rate and blood pressure, which eases the workload on the heart.

Metoprolol succinate selectively blocks β1‑adrenergic receptors in the heart, reducing the effects of adrenaline and noradrenaline. This leads to a slower heart rate, decreased contractility, and lower blood pressure, helping to control cardiovascular stress.

The appropriate dose of Metoprolol Succinate Tad is determined by the prescribing clinician based on the patient’s medical condition, response to therapy, and other individual factors. Dosage adjustments are made during follow‑up visits.

Safety information for Metoprolol Succinate Tad in pregnancy and lactation is limited. Healthcare providers should weigh potential benefits against possible risks and consider alternative therapies when appropriate.

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 succinate is a cardio‑selective (β1‑specific) blocker, offering a lower risk of bronchospasm compared with non‑selective agents. Its extended‑release formulation provides once‑daily dosing, which can improve adherence relative to short‑acting beta blockers.

Store Metoprolol Succinate Tad at temperatures below 25 °C. Keep the tablets in the original packaging, protect them from moisture and direct sunlight, and ensure they are out of reach of children.

Metoprolol Succinate Tad is taken orally, usually once daily with or without food, as directed by the prescriber. Swallow the tablet whole; do not crush, split or chew it unless specifically instructed.

Serious risks include severe bradycardia, heart block, marked hypotension, bronchospasm in susceptible individuals, and rare allergic reactions. Patients should seek immediate medical attention if they experience fainting, severe dizziness, difficulty breathing, or swelling of the face or throat.

Metoprolol Succinate Tad 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 in cardiogenic shock.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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