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 an antiparkinson agent (dopamine precursor with dopa decarboxylase inhibitor) presented as an oral tablet for oral use. It is used to manage the motor symptoms of Parkinson's disease and related Parkinsonian syndromes in adult patients.

GNH India supplies Madopar as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing reliable sourcing, regulatory documentation and temperature‑controlled logistics where required. All batches are manufactured under EU Good Manufacturing Practice standards and undergo rigorous quality testing before release.

Manufacturer / TM Owner

Roche Pharmaceuticals A/S

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Indications & Clinical Uses

Madopar is an antiparkinson medication that targets dopaminergic pathways to improve motor control in Parkinsonian disorders.

  • Parkinson's disease: improves motor function, reduces rigidity, tremor and bradykinesia.
  • Parkinsonian syndrome: alleviates symptoms associated with secondary or atypical parkinsonism.
  • Drug‑induced or vascular Parkinsonism: provides symptomatic relief when dopaminergic deficit is present.

How It Works

  • Levodopa crosses the blood‑brain barrier and is decarboxylated to dopamine within the central nervous system, restoring deficient dopaminergic transmission. Benserazide, a peripheral aromatic L‑amino acid decarboxylase inhibitor, blocks peripheral conversion of levodopa, increasing its availability to the brain and minimizing peripheral side effects.

Side Effects

Common Side Effects

  • Nausea: gastrointestinal upset occurring shortly after dosing.
  • Orthostatic hypotension: dizziness or light‑headedness upon standing.
  • Insomnia: difficulty falling or staying asleep.
  • Dyskinesia: involuntary movements that may develop with long‑term use.
  • Dry mouth: reduced salivation leading to discomfort.
  • Headache: mild to moderate pain often transient.

Serious or Rare Side Effects

  • Severe hypotension: marked blood‑pressure drop requiring medical attention.
  • Psychiatric disturbances: hallucinations, confusion or depression.
  • Cardiac arrhythmias: irregular heart rhythms that may be life‑threatening.
  • Allergic reactions: rash, swelling or anaphylaxis.
  • Neuroleptic malignant syndrome: rare but potentially fatal reaction when combined with antipsychotics.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate cardiovascular status and renal function, and consider potential interactions with other medications.

  • Monitor blood pressure: levodopa can cause orthostatic hypotension.
  • Assess for dyskinesia: adjust dose if involuntary movements appear.
  • Adjust dose in renal impairment: reduced clearance may increase exposure.
  • Avoid abrupt discontinuation: taper to prevent withdrawal syndrome.
  • Use with caution in elderly patients: increased sensitivity to side effects.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Madopar may interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • Non‑selective MAO inhibitors: risk of hypertensive crisis.
  • Antipsychotics (e.g., haloperidol): may diminish levodopa efficacy.
  • High‑dose pyridoxine (vitamin B6): reduces levodopa absorption.

Moderate Interactions (Monitor Closely)

  • Antihypertensives: may enhance orthostatic hypotension.
  • SSRIs or SNRIs: potential for serotonin syndrome.
  • Iron or calcium supplements: can decrease levodopa bioavailability.

Frequently Asked Questions

Madopar is prescribed to treat the motor symptoms of Parkinson's disease and other Parkinsonian syndromes. It helps reduce tremor, rigidity, and bradykinesia by restoring dopamine levels in the brain, thereby improving patients' daily functioning.

Levodopa is a precursor that crosses the blood‑brain barrier and is converted into dopamine, the neurotransmitter lacking in Parkinson's disease. Benserazide blocks peripheral conversion, allowing more levodopa to reach the brain and produce a therapeutic effect.

The dose of Madopar is individualized and set by the prescribing clinician based on disease severity, patient age, and response. Dosage adjustments are made during treatment to balance symptom control with tolerability.

The pregnancy category for Madopar is unknown, and safety data are limited. It should only be used if the potential benefit justifies the potential risk to the fetus. Breastfeeding mothers should consult their physician, as levodopa can be excreted in milk.

To order 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, offering more consistent brain delivery than levodopa alone and fewer peripheral side effects than formulations without a decarboxylase inhibitor. Compared with dopamine agonists, it provides stronger symptomatic relief but may have a higher risk of motor complications over long‑term use.

Madopar tablets should be stored at room temperature, below 25 °C, in the original packaging to protect them from moisture and light. Keep the product out of reach of children and avoid storing in humid or excessively hot environments.

Madopar is taken orally, usually with a glass of water. It can be taken with or without food, but a consistent routine helps maintain stable plasma levels. Tablets should be swallowed whole; they are not intended for crushing or chewing.

Serious risks include severe hypotension, psychiatric disturbances such as hallucinations or depression, cardiac arrhythmias, and rare allergic reactions like anaphylaxis. Patients should be monitored closely for these events, especially during dose escalations or when combined with interacting medications.

Madopar is contraindicated in patients with known hypersensitivity to levodopa or benserazide, those with narrow‑angle glaucoma, severe cardiovascular disease, or those currently taking non‑selective MAO inhibitors. Caution is also advised for individuals with a history of malignant melanoma or severe hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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