Product image of Metoprololsuccinat Mylan (Metoprolol Tartrate) supplied by GNH India

Metoprololsuccinat Mylan

Active Ingredient:
Metoprolol Tartrate
Origin:
EU

Metoprololsuccinat Mylan (Metoprolol Tartrate)

Metoprolol Tartrate, the active ingredient in Metoprololsuccinat Mylan, is a beta blocker presented as an oral tablet for oral use. It is employed to lower blood pressure, relieve angina, and improve outcomes in heart failure and post‑myocardial infarction patients.
GNH India supplies Metoprololsuccinat Mylan as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Mylan Germany Gmbh

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Indications & Clinical Uses

Metoprolol Tartrate is a selective β1‑adrenergic antagonist used in several cardiovascular conditions.

  • Hypertension: reduces systolic and diastolic pressure by decreasing cardiac output.
  • Angina pectoris: lowers myocardial oxygen demand, relieving chest pain.
  • Post‑myocardial infarction: improves survival by limiting arrhythmias and remodeling.
  • Chronic heart failure: enhances ventricular function and reduces hospitalisation.
  • Certain cardiac arrhythmias: controls heart rate by slowing atrioventricular conduction.

How It Works

  • Metoprolol Tartrate selectively blocks β1‑adrenergic receptors in cardiac tissue, inhibiting catecholamine‑induced stimulation. This results in a slower heart rate, reduced myocardial contractility, and lower stroke volume, which together decrease cardiac output and systemic blood pressure while also diminishing myocardial oxygen consumption.

Side Effects

Metoprolol Tartrate may cause a range of adverse reactions.

Common Side Effects

  • Fatigue or tiredness
  • Dizziness or light‑headedness
  • Bradycardia (slow heart rate)
  • Gastrointestinal discomfort such as nausea or abdominal pain

Serious or Rare Side Effects

  • Severe bradycardia or heart block
  • Marked hypotension
  • Bronchospasm, especially in patients with asthma or COPD
  • Allergic reactions including rash, swelling or anaphylaxis
  • Depression or mood changes
  • Worsening heart failure symptoms

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor for adverse events.

  • Blood pressure monitoring: ensure adequate control without excessive hypotension.
  • Cardiac function assessment: review baseline heart rate and ejection fraction.
  • Respiratory caution: avoid in uncontrolled asthma or severe COPD.
  • Drug review: consider interactions with other rate‑controlling agents.
  • Renal impairment: dose adjustment may be required in reduced clearance.
  • Store at ambient temperature: keep in the original pack, protect from moisture.

Avoid Interactions

Metoprolol Tartrate can interact with several medicines, altering its efficacy or safety.

Major Interactions (Avoid)

  • Concomitant use with other AV‑node blockers (e.g., verapamil, diltiazem) may cause profound bradycardia.
  • Abrupt discontinuation of clonidine while on metoprolol can precipitate hypertension.
  • Potent CYP2D6 inhibitors (e.g., quinidine, fluoxetine) increase metoprolol plasma levels.

Moderate Interactions (Monitor Closely)

  • Diuretics: may enhance hypotensive effect, requiring blood pressure checks.
  • Antidiabetic agents: metoprolol can mask hypoglycaemia symptoms, necessitating glucose monitoring.

Frequently Asked Questions

Metoprololsuccinat Mylan contains metoprolol tartrate, a selective β1‑blocker indicated for hypertension, chronic stable angina, post‑myocardial infarction management, chronic heart failure, and certain supraventricular arrhythmias. It works by lowering heart rate and myocardial workload, helping to control blood pressure and reduce cardiac oxygen demand.

Metoprolol tartrate selectively antagonises β1‑adrenergic receptors in the heart. By blocking the effects of adrenaline and noradrenaline, it slows the sinus node, reduces contractile force, and lowers cardiac output, which together lower systemic blood pressure and decrease myocardial oxygen consumption.

The appropriate dose is determined by the prescribing clinician based on the individual’s condition, age, renal function and response to therapy. Dosage may be started low and titrated upward, but exact regimens should only be set by a qualified healthcare professional.

Safety data are limited, and the pregnancy category is listed as unknown. Because β‑blockers can affect fetal growth and neonatal heart rate, the drug should only be used during pregnancy or lactation when the potential benefit justifies the potential risk and after consultation with a specialist.

To place an order, visit the product page on gnhindia.com, submit an enquiry with the required quantity, and provide institutional or trade credentials. GNH India’s commercial team will verify eligibility, then respond with pricing, availability, shipping details (including any cold‑chain requirements) and the necessary import documentation.

Metoprolol is a cardio‑selective (β1‑specific) blocker, offering fewer respiratory side effects than non‑selective agents such as propranolol. It is commonly preferred for patients with hypertension or heart failure who also have mild asthma or COPD, whereas non‑selective blockers may be chosen for migraine prophylaxis or essential tremor.

Store the tablets at ambient temperature, preferably below 25 °C, in the original container to protect from moisture and light. Keep out of reach of children and do not use after the expiry date printed on the packaging.

The medication is taken orally, usually with a glass of water. It may be taken with or without food, but consistency with meals helps maintain stable absorption. Patients should follow the prescriber’s instructions regarding timing and whether the dose is taken once or twice daily.

Serious adverse events include severe bradycardia, heart block, marked hypotension, bronchospasm in susceptible individuals, and rare allergic reactions such as anaphylaxis. Patients should seek immediate medical attention if they experience fainting, severe shortness of breath, chest pain, or signs of an allergic response.

Metoprolol is contraindicated in patients with known hypersensitivity to the drug, those with severe bradycardia (heart rate < 45 bpm), second‑ or third‑degree atrioventricular block without a pacemaker, cardiogenic shock, and uncontrolled asthma or severe chronic obstructive pulmonary disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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