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

Madopar Cr

Active Ingredient:
Benserazide, Levodopa
Origin:
EU

Madopar Cr (Benserazide, Levodopa)

Levodopa / Benserazide, the active ingredients in Madopar CR, are a combination of a dopamine precursor and a DOPA decarboxylase inhibitor presented as a controlled‑release oral tablet for oral use. They are employed to treat Parkinson's disease and related Parkinsonian syndromes by restoring central dopamine levels.

GNH India supplies Madopar CR 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, ensuring product integrity throughout the supply chain.

Manufacturer / TM Owner

Roche Products Ltd

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Indications & Clinical Uses

Madopar CR is indicated for the management of Parkinsonian disorders, addressing dopamine deficiency in the central nervous system.

  • Parkinson's disease: improves motor function, reduces rigidity, bradykinesia and tremor, enhancing daily activities.
  • Parkinsonian syndrome: alleviates symptoms such as stiffness and slowed movement caused by secondary causes.
  • Secondary Parkinsonism: restores dopaminergic tone to mitigate drug‑induced or vascular Parkinsonian features.

How It Works

  • Madopar CR delivers levodopa, a dopamine precursor, which crosses the blood‑brain barrier and is decarboxylated to dopamine within the central nervous system. Benserazide, a peripheral aromatic L‑amino acid decarboxylase inhibitor, blocks the conversion of levodopa to dopamine outside the brain, increasing the amount of levodopa that reaches the CNS and prolonging its therapeutic effect. The combined action results in more stable plasma levodopa concentrations and smoother motor control.

Side Effects

Common and serious adverse reactions have been reported with levodopa/benserazide therapy.

Common Side Effects

  • Nausea: gastrointestinal upset occurring early in treatment.
  • Vomiting: may accompany nausea or occur independently.
  • Dizziness: often related to orthostatic changes.
  • Orthostatic hypotension: drop in blood pressure upon standing.
  • Headache: mild to moderate intensity.
  • Insomnia: difficulty initiating or maintaining sleep.

Serious or Rare Side Effects

  • Dyskinesia: involuntary, erratic movements affecting limbs or trunk.
  • Hallucinations: visual or auditory perceptual disturbances.
  • Severe hypotension: marked blood pressure fall requiring medical attention.
  • Neuroleptic malignant syndrome: rare life‑threatening reaction.
  • Cardiac arrhythmias: irregular heart rhythms observed in susceptible patients.
  • Anaphylaxis: acute allergic reaction with airway compromise.

Precautions & Warnings

When prescribing Madopar CR, clinicians should consider several safety precautions to minimize risks.

  • Dose titration: start low and increase gradually to reduce gastrointestinal and cardiovascular side effects.
  • Renal impairment: adjust therapy and monitor renal function as excretion may be affected.
  • Cardiovascular disease: observe blood pressure and heart rate for orthostatic changes.
  • Psychiatric history: watch for emergence of hallucinations or psychosis.
  • Concomitant drugs: review all medications for potential interactions that may alter levodopa efficacy.
  • Store at ambient temperature below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Madopar CR can interact with other medicines, influencing its effectiveness or safety.

Major Interactions (Avoid)

  • Non‑selective MAO inhibitors: may cause hypertensive crisis when combined with levodopa.
  • Antipsychotics that block D2 receptors: reduce therapeutic benefit of levodopa.
  • Irreversible MAO‑B inhibitors: increase levodopa plasma levels and risk of toxicity.

Moderate Interactions (Monitor Closely)

  • Antihypertensive agents: additive effect on blood pressure leading to hypotension.
  • SSRIs or SNRIs: potential for serotonin syndrome when used with MAO inhibitors.
  • Diuretics: may enhance orthostatic hypotension and electrolyte disturbances.

Frequently Asked Questions

Madopar CR is a prescription medication that combines levodopa and benserazide to treat Parkinson's disease and other Parkinsonian syndromes. It helps replenish dopamine in the brain, reducing motor symptoms such as tremor, rigidity, and slowed movement, thereby improving patients' daily functioning.

Levodopa is a precursor of dopamine that crosses the blood‑brain barrier. Once inside the central nervous system it is converted to dopamine, compensating for the deficiency that characterises Parkinsonian disorders. Benserazide blocks peripheral conversion, allowing more levodopa to reach the brain.

The exact dose of Madopar CR is individualized and set by a qualified prescriber. Dosing depends on factors such as disease severity, patient age, response to therapy, and the presence of other medical conditions. Patients should follow the prescribing clinician's instructions without self‑adjusting the dose.

Safety data for Madopar CR 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. Women who are pregnant, planning pregnancy, or breastfeeding should discuss alternatives with their healthcare provider.

To request Madopar CR, 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 CR provides a controlled‑release delivery of levodopa, resulting in more stable plasma concentrations and fewer peaks and troughs compared with immediate‑release tablets. This can lead to reduced motor fluctuations and a lower incidence of certain side effects, although individual response varies and the choice of formulation is guided by clinical judgment.

Madopar CR tablets should be stored at ambient temperature below 25 °C. Keep them in the original blister pack, protect from moisture and direct sunlight, and ensure the container is tightly closed to maintain tablet integrity throughout its shelf life.

Madopar CR is taken orally as a whole tablet with a full glass of water. It should be swallowed whole and not crushed, chewed, or broken, to preserve the controlled‑release mechanism. Dosing times are usually spaced evenly throughout the day as directed by the prescriber.

Serious adverse events include dyskinesia (involuntary movements), hallucinations or psychosis, severe hypotension, neuroleptic malignant syndrome, cardiac arrhythmias, and rare allergic reactions such as anaphylaxis. Patients should be monitored closely for these events, and any concerning symptoms should prompt immediate medical evaluation.

Madopar CR is contraindicated in individuals with known hypersensitivity to levodopa, benserazide, or any excipients. It should also be avoided in patients currently taking non‑selective MAO inhibitors or those who have experienced severe reactions to similar antiparkinson agents. Clinicians must assess each patient’s medical history before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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