Product image of Madopar (Benserazide Hydrochloride, Levodopa) supplied by GNH India

Madopar

Active Ingredient:
Benserazide Hydrochloride, Levodopa
Origin:
EU

Madopar (Benserazide Hydrochloride, Levodopa)

Levodopa/Benserazide Hydrochloride, the active ingredients in Madopar, are antiparkinson agents presented as oral tablets for oral use. They are prescribed to manage the motor symptoms of Parkinson's disease and related Parkinsonian syndromes by increasing dopamine availability in the brain.

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

Manufacturer / TM Owner

Roche S. R. O.

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Indications & Clinical Uses

Madopar is used in the management of Parkinsonian disorders, targeting dopaminergic pathways to improve motor function.

  • Parkinson's disease: reduces rigidity, bradykinesia and tremor, enhancing daily activity performance.
  • Parkinsonian syndrome: alleviates motor deficits caused by idiopathic or secondary Parkinsonism.
  • Drug‑induced Parkinsonism: mitigates symptoms when antipsychotic‑induced dopamine blockade is present.

How It Works

  • Levodopa is a precursor that crosses the blood‑brain barrier and is decarboxylated to dopamine within central neurons. Benserazide, a peripheral dopa decarboxylase inhibitor, prevents conversion of levodopa outside the brain, thereby increasing the amount of levodopa that reaches the central nervous system and enhancing dopaminergic neurotransmission.

Side Effects

Madopar may cause a range of adverse reactions, most of which are dose‑related and reversible upon adjustment.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Orthostatic hypotension: dizziness upon standing.
  • Dyskinesia: involuntary movements, especially at higher doses.
  • Insomnia: difficulty initiating or maintaining sleep.
  • Dry mouth: reduced salivation.
  • Mood changes: anxiety or depression.

Serious or Rare Side Effects

  • Neuroleptic malignant syndrome: life‑threatening hyperthermia and rigidity.
  • Severe cardiac arrhythmias: rare but potentially fatal.
  • Hallucinations: visual or auditory disturbances.
  • Severe orthostatic hypotension leading to falls.

Precautions & Warnings

When prescribing Madopar, clinicians should consider patient‑specific factors and monitor for adverse events.

  • Renal impairment: adjust dose as clearance may be reduced.
  • Hepatic dysfunction: use caution due to altered metabolism.
  • Concomitant MAO‑B inhibitors: avoid combined use to reduce risk of hypertensive crisis.
  • Pregnancy and lactation: safety not established; weigh benefits against potential risks.
  • Elderly patients: start with low dose and titrate slowly to minimize dyskinesia.
  • Store at ambient temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Madopar interacts with several drug classes that can alter its efficacy or safety profile.

Major Interactions (Avoid)

  • Non‑selective MAO inhibitors (e.g., phenelzine): risk of hypertensive crisis.
  • Antipsychotics with strong D2 antagonism (e.g., haloperidol): may negate therapeutic effect.
  • High‑dose pyridoxine (vitamin B6): accelerates peripheral levodopa metabolism.

Moderate Interactions (Monitor Closely)

  • Antihypertensives: may enhance orthostatic hypotension.
  • Iron or calcium supplements: can reduce levodopa absorption; separate dosing by at least 2 hours.
  • SSRIs and SNRIs: may increase risk of serotonin syndrome when combined with MAO‑B inhibitors.

Frequently Asked Questions

Madopar is prescribed to treat Parkinson's disease and other Parkinsonian syndromes. It helps improve motor symptoms such as tremor, rigidity, and bradykinesia by increasing dopamine levels in the brain.

Levodopa serves as a dopamine precursor that crosses the blood‑brain barrier and is converted to dopamine in the central nervous system. Benserazide inhibits peripheral dopa decarboxylase, preventing premature conversion of levodopa outside the brain, thereby enhancing central dopamine availability.

The appropriate dose of Madopar is individualized and set by the prescribing clinician based on the patient’s condition, response, and tolerability. Dosage regimens vary and should follow the prescriber’s instructions.

Safety of Madopar in pregnancy and lactation has not been established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To order Madopar, 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 any necessary import documentation.

Madopar combines levodopa with benserazide, offering higher central dopamine delivery compared with levodopa alone. Compared with dopamine agonists, it provides more potent symptom control but may have a higher risk of motor complications such as dyskinesia.

Madopar tablets should be stored at ambient temperature, below 25 °C. Keep them in the original packaging, protect from moisture and direct sunlight, and ensure the container is tightly closed.

Madopar is taken orally, usually with a small amount of food to reduce gastrointestinal irritation. Tablets should be swallowed whole with water and not crushed or chewed unless specifically directed by a healthcare provider.

Serious risks include neuroleptic malignant syndrome, severe orthostatic hypotension leading to falls, and rare cardiac arrhythmias. Patients should be monitored for sudden changes in blood pressure, temperature, or mental status.

Madopar is contraindicated in patients taking non‑selective MAO inhibitors, those with known hypersensitivity to levodopa or benserazide, and individuals with severe cardiovascular disease where rapid blood pressure changes could be hazardous.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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