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

Madopar

Active Ingredient:
Benserazide, Levodopa
Origin:
EU

Madopar (Benserazide, Levodopa)

Levodopa/Benserazide, the active ingredient in Madopar, is an antiparkinson agent presented as oral tablets for oral use. It is employed to manage the motor symptoms of Parkinson's disease and related Parkinsonian syndromes in adult patients. The combination provides central dopamine replacement while limiting peripheral conversion, thereby improving efficacy and tolerability.

GNH India supplies Madopar as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. Our global distribution network ensures consistent quality and regulatory compliance across markets.

Manufacturer / TM Owner

Roche Pharmaceuticals A/S

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Indications & Clinical Uses

Madopar is an antiparkinson medication that acts on dopaminergic pathways to alleviate motor dysfunction.

  • Parkinson's disease: improves bradykinesia, rigidity, and tremor in patients with idiopathic Parkinson's disease.
  • Parkinsonian syndrome: reduces motor symptoms in secondary or atypical parkinsonian disorders responsive to levodopa.
  • Resting tremor: diminishes tremor amplitude and frequency associated with levodopa‑responsive conditions.

How It Works

  • Levodopa crosses the blood‑brain barrier and is decarboxylated to dopamine, replenishing depleted central dopamine stores. Benserazide, a peripheral dopa‑decaboxylase inhibitor, prevents conversion of levodopa to dopamine outside the brain, increasing the amount of levodopa that reaches the central nervous system and reducing peripheral side effects such as nausea and hypotension.

Side Effects

Common Side Effects

  • Nausea or vomiting
  • Orthostatic hypotension
  • Dyskinesia (involuntary movements)
  • Drowsiness or fatigue
  • Dry mouth
  • Loss of appetite

Serious or Rare Side Effects

  • Severe hypertension or hypertensive crisis
  • Neuroleptic malignant syndrome when combined with dopamine antagonists
  • Cardiac arrhythmias
  • Severe psychiatric disturbances (hallucinations, psychosis)
  • Allergic reactions (rash, angioedema)

Precautions & Warnings

Madopar should be used with caution in specific clinical situations.

  • Monitor blood pressure: watch for orthostatic hypotension, especially during dose titration.
  • Adjust dose gradually: avoid abrupt discontinuation to prevent withdrawal symptoms.
  • Assess hepatic function: use caution in patients with liver impairment.
  • Use carefully in the elderly: increased susceptibility to dizziness and falls.
  • Avoid concomitant non‑selective MAO inhibitors: risk of hypertensive crisis.
  • Store at room temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Madopar may interact with several medicines, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Non‑selective MAO inhibitors (e.g., phenelzine): can cause hypertensive crisis.
  • Dopamine antagonists (e.g., typical antipsychotics): may reduce therapeutic effect and precipitate severe reactions.
  • High‑dose pyridoxine (vitamin B6): accelerates peripheral decarboxylation of levodopa.

Moderate Interactions (Monitor Closely)

  • Antihypertensive agents: additive blood‑pressure lowering effect.
  • Selective serotonin reuptake inhibitors (SSRIs): may increase risk of serotonin syndrome.
  • Iron or calcium supplements: may reduce levodopa absorption; separate administration by at least 2 hours.
  • Anticholinergic drugs: may mask some motor side effects but increase confusion in the elderly.

Frequently Asked Questions

Madopar is prescribed to treat the motor symptoms of Parkinson's disease and other Parkinsonian syndromes. It helps improve movement, reduce rigidity, and control tremor by restoring dopamine levels in the brain.

Levodopa is converted into dopamine within the brain, replenishing the neurotransmitter that is deficient in Parkinsonian disorders. Benserazide inhibits the peripheral conversion of levodopa, ensuring more of the drug reaches the central nervous system and minimizing peripheral side effects.

The dosage of Madopar is individualized. A qualified prescriber determines the appropriate strength, frequency, and titration schedule based on the patient’s clinical condition, response, and tolerability.

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

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 necessary import documentation.

Madopar combines levodopa with benserazide, a peripheral decarboxylase inhibitor, which can offer better central availability and reduced peripheral side effects compared with levodopa alone. This may allow lower dosing and improved tolerability for some patients.

Madopar tablets should be stored at room temperature, below 25 °C. Keep them in the original packaging, protect from moisture and direct sunlight, and ensure they are out of reach of children.

Madopar is taken orally, usually with a small amount of water. It is often recommended to take the medication with food to reduce gastrointestinal irritation, but timing relative to meals should follow the prescriber’s guidance.

Serious risks include severe hypertension, neuroleptic malignant syndrome when combined with dopamine antagonists, cardiac arrhythmias, and significant psychiatric disturbances such as hallucinations or psychosis. Patients should be monitored closely for these events.

Madopar is contraindicated in patients with known hypersensitivity to levodopa, benserazide, or any excipients, and in those taking non‑selective MAO inhibitors. Caution is also advised for individuals with severe cardiovascular disease, uncontrolled hypertension, or a history of malignant neuroleptic syndrome.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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