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

Madopar

Active Ingredient:
Benserazide Hydrochloride, Levodopa
Origin:
EU

Madopar (Benserazide Hydrochloride, Levodopa)

Levodopa, the active ingredient in Madopar, is a dopamine precursor presented as an oral tablet for oral use. In combination with benserazide hydrochloride, it forms a dopamine precursor and dopa decarboxylase inhibitor that restores deficient central dopamine, thereby improving motor function in adults with Parkinson's disease and Parkinsonian syndromes.

GNH India supplies Madopar as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing reliable sourcing, regulatory documentation and logistics support for global health care providers and patients.

Manufacturer / TM Owner

Roche Farmacevtska Družba D.O.O.

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Indications & Clinical Uses

Madopar acts on dopaminergic pathways to alleviate motor symptoms associated with Parkinsonian disorders.

  • Parkinson's disease: improves tremor, rigidity, bradykinesia and overall motor function.
  • Parkinsonian syndrome: reduces motor impairment caused by secondary or atypical Parkinsonism.
  • Levodopa‑responsive Parkinsonism: restores dopamine levels to achieve symptomatic control.

How It Works

  • Madopar combines levodopa, a precursor that crosses the blood‑brain barrier and is enzymatically converted to dopamine, with benserazide, a peripheral aromatic L‑amino‑acid decarboxylase inhibitor. Benserazide blocks peripheral conversion of levodopa, increasing its availability to the central nervous system, where levodopa is decarboxylated to dopamine, thereby augmenting deficient dopaminergic neurotransmission in the basal ganglia. The resulting increase in dopamine activity helps normalize motor circuit signaling and reduces the characteristic symptoms of Parkinsonism.

Side Effects

Madopar may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Nausea: upset stomach often occurring at treatment initiation.
  • Orthostatic hypotension: dizziness or light‑headedness upon standing.
  • Insomnia: difficulty falling or staying asleep.
  • Dyskinesia: involuntary movements, especially with higher doses.

Serious or Rare Side Effects

  • Severe hypotension: marked blood pressure drop requiring medical attention.
  • Psychosis or hallucinations: visual or auditory disturbances in susceptible patients.
  • Allergic reactions: rash, swelling, or anaphylaxis in rare cases.

Precautions & Warnings

When prescribing Madopar, clinicians should consider several precautionary measures to optimize safety.

  • Dose titration: start with the lowest effective dose and increase gradually to minimize side effects.
  • Blood pressure monitoring: watch for orthostatic hypotension, especially in elderly patients.
  • Psychiatric assessment: monitor for hallucinations, confusion, or mood changes.
  • Drug discontinuation: avoid abrupt cessation to prevent worsening of Parkinsonian symptoms.
  • Concomitant medications: review all patient medicines for potential interactions.
  • Store at ambient temperature: keep tablets in the original container, protect from moisture and heat.

Avoid Interactions

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

Major Interactions (Avoid)

  • Non‑selective MAO inhibitors (e.g., phenelzine): may cause hypertensive crisis.
  • Antipsychotics (e.g., haloperidol): block dopamine receptors and reduce therapeutic effect.
  • Pyridoxine (vitamin B6): enhances peripheral levodopa metabolism, decreasing central availability.

Moderate Interactions (Monitor Closely)

  • Antihypertensive drugs: additive blood‑pressure‑lowering effect may increase dizziness.
  • Iron or calcium supplements: can reduce levodopa absorption if taken simultaneously.
  • High‑protein meals: compete with levodopa for intestinal transport, potentially diminishing efficacy.

Frequently Asked Questions

Madopar is prescribed to manage the motor symptoms of Parkinson's disease and Parkinsonian syndromes. By increasing dopamine levels in the brain, it helps reduce tremor, stiffness, slowness of movement, and improves overall functional ability in adult patients.

Levodopa is a chemical precursor that crosses the blood‑brain barrier and is converted into dopamine within the central nervous system. The added benserazide blocks peripheral conversion, ensuring more levodopa reaches the brain where it restores deficient dopaminergic neurotransmission.

The appropriate dose of Madopar is individualized and determined by the prescribing clinician based on the patient’s condition, response, and tolerability. Dosage regimens are not standardized and should follow the prescriber’s instructions.

Safety data for Madopar in pregnancy and lactation are limited. It should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To request Madopar, 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.

Madopar combines levodopa with benserazide, a peripheral decarboxylase inhibitor, similar to the levodopa/carbidopa combination. Both strategies increase central levodopa availability while reducing peripheral side effects. Choice between them depends on physician preference, patient tolerance, and specific formulation availability.

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

Madopar is taken orally, usually with a glass of water. It is often recommended to take the medication on an empty stomach or as directed by the prescriber to optimize absorption, and doses are spaced throughout the day according to the treatment plan.

Serious adverse events include severe hypotension, which can cause fainting; neuropsychiatric effects such as hallucinations or psychosis; and rare allergic reactions that may present as rash, swelling or anaphylaxis. Prompt medical attention is required if any of these occur.

Madopar is contraindicated in patients with known hypersensitivity to levodopa, benserazide, or any excipients, as well as those with narrow‑angle glaucoma, malignant melanoma, or a history of severe cardiovascular disease where dopamine‑related effects could be harmful.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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