Product image of Moduxin Mr (Trimetazidine Dihydrochloride) supplied by GNH India

Moduxin Mr

Active Ingredient:
Trimetazidine Dihydrochloride
Origin:
EU

Moduxin Mr (Trimetazidine Dihydrochloride)

Trimetazidine Dihydrochloride, the active ingredient in Moduxin MR, is a pimodazole derivative (anti‑ischemic metabolic agent) presented as a modified‑release tablet for oral use. It is indicated for the management of stable angina pectoris and other forms of coronary artery disease in adult patients.

GNH India supplies Moduxin MR as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable logistics for global distribution. Customers benefit from consistent supply chains and regulatory compliance support.

Manufacturer / TM Owner

Gedeon Richter Plc.

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Indications & Clinical Uses

Trimetazidine is used in the anti‑ischemic therapeutic area to improve myocardial energy metabolism in coronary artery disease.

  • Stable angina pectoris: reduces the frequency of angina attacks and improves exercise tolerance.
  • Chronic coronary syndrome: helps alleviate chest discomfort during daily activities.
  • Ischemic heart disease: supports myocardial function by enhancing ATP production under ischemic conditions.

How It Works

  • Trimetazidine selectively inhibits the mitochondrial long‑chain 3‑ketoacyl‑CoA thiolase, reducing fatty‑acid β‑oxidation in cardiac myocytes. This metabolic shift favors glucose oxidation, which requires less oxygen per ATP generated, thereby improving cellular energy efficiency during ischemia. By preserving intracellular ion balance and limiting lactate accumulation, the drug further protects the heart from ischemic injury.

Side Effects

Trimetazidine may be associated with several adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Headache: transient pain often reported.
  • Dizziness: sensation of light‑headedness, especially on standing.
  • Gastrointestinal discomfort: abdominal pain or dyspepsia.
  • Fatigue: feeling of reduced energy.
  • Skin rash: mild erythema or itching.

Serious or Rare Side Effects

  • Severe allergic reactions: anaphylaxis, swelling of face or throat.
  • Extrapyramidal symptoms: tremor, rigidity, or parkinsonian features.
  • Liver enzyme elevation: significant increase in transaminases indicating hepatic stress.
  • Hematologic abnormalities: rare cases of leukopenia or thrombocytopenia.
  • Cardiac arrhythmias: uncommon but potentially life‑threatening rhythm disturbances.

Precautions & Warnings

When prescribing Trimetazidine, clinicians should observe the following precautions to ensure safe use.

  • Cardiac monitoring: assess patient’s angina status and ECG periodically.
  • Renal impairment: use with caution in severe renal dysfunction; dose adjustment may be required.
  • Elderly patients: monitor for dizziness or hypotension due to increased sensitivity.
  • Allergic reactions: discontinue immediately if signs of hypersensitivity such as rash or swelling appear.
  • Store at room temperature: keep tablets in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Trimetazidine can interact with other medicines; awareness of major and moderate interactions helps avoid adverse outcomes.

Major Interactions (Avoid)

  • Concomitant use with other anti‑ischemic agents that cause profound hypotension (e.g., high‑dose nitrates) may increase risk of low blood pressure.
  • Combination with drugs that strongly inhibit mitochondrial enzymes (e.g., certain antiretrovirals) may potentiate metabolic effects.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may enhance anti‑anginal effect, requiring clinical monitoring.
  • Calcium channel blockers: monitor for additive effects on heart rate and blood pressure.
  • Selective serotonin reuptake inhibitors: observe for possible increase in dizziness.

Frequently Asked Questions

Moduxin MR contains trimetazidine dihydrochloride and is prescribed to manage stable angina pectoris, chronic coronary syndrome, and other forms of ischemic heart disease. It works by improving the efficiency of myocardial energy production, which helps reduce chest pain episodes and enhances exercise tolerance in patients with coronary artery disease.

Trimetazidine selectively inhibits the mitochondrial enzyme responsible for long‑chain fatty‑acid β‑oxidation. By shifting cardiac metabolism toward glucose oxidation, the heart generates more ATP per unit of oxygen consumed. This metabolic optimization preserves myocardial contractility and reduces ischemic symptoms during periods of reduced blood flow.

The appropriate dose of Moduxin MR is individualized by the prescribing healthcare professional based on the patient’s clinical condition, severity of angina, and response to therapy. Dosage adjustments may be considered for renal impairment or other comorbidities, but specific regimens should only be set by a qualified prescriber.

Safety data for trimetazidine during pregnancy and lactation are limited, and the product is generally classified as contraindicated or to be used only if the potential benefit justifies the potential risk. Women who are pregnant, planning to become pregnant, or breastfeeding should discuss alternative therapies with their physician.

To request Moduxin MR, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams across international markets, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including any cold‑chain requirements) and the necessary import documentation.

The primary alternative to trimetazidine is ranolazine, another anti‑ischemic agent. While both improve myocardial metabolism, ranolazine primarily inhibits the late sodium current, whereas trimetazidine shifts substrate utilization toward glucose. Clinical choice depends on patient tolerance, drug‑specific side‑effect profiles, and physician preference.

Moduxin MR tablets should be stored at room temperature, below 25 °C, in the original packaging. Protect the product from moisture, excessive heat, and direct sunlight to maintain stability and efficacy throughout its shelf life.

Moduxin MR is taken orally as a modified‑release tablet. Patients should swallow the tablet whole with a glass of water and avoid crushing or chewing it, as this could alter the release characteristics and affect therapeutic outcomes.

Serious adverse events, although rare, include severe allergic reactions such as anaphylaxis, extrapyramidal symptoms resembling Parkinson’s disease, and significant liver enzyme elevations indicating possible hepatic injury. Prompt medical attention is required if any of these symptoms develop.

Moduxin MR should be avoided in patients with known hypersensitivity to trimetazidine or any tablet excipients, those with severe renal impairment where dose adjustment is not feasible, and individuals who have experienced serious extrapyramidal reactions to similar metabolic agents. Consultation with a healthcare professional is essential before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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