Product image of Motetis (Tetrabenazine) supplied by GNH India

Motetis

Active Ingredient:
Tetrabenazine
Origin:
EU

Motetis (Tetrabenazine)

Tetrabenazine, the active ingredient in Motetis, is a VMAT2 inhibitor presented as an oral formulation for oral use. It is indicated for adult patients with hyperkinetic movement disorders such as Huntington's disease and tardive dyskinesia, helping to reduce involuntary movements that interfere with daily activities.

GNH India supplies Motetis as a licensed, GDP‑compliant international pharmaceutical supplier, delivering quality‑assured medication to hospitals, pharmacies and clinics worldwide in accordance with EU regulatory standards and supports reliable supply chains for global healthcare providers.

Manufacturer / TM Owner

Walter Ritter Gmbh + Co. Kg

1
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Indications & Clinical Uses

  • Motetis (tetrabenazine) acts on the vesicular monoamine transporter 2 pathway to control abnormal involuntary movements.
  • Huntington's disease (chorea): reduces the severity and frequency of choreiform movements, improving motor function.
  • Tardive dyskinesia (drug‑induced involuntary movements): decreases the intensity of facial and limb dyskinesias.
  • Other hyperkinetic movement disorders (off‑label): may provide symptomatic relief of involuntary movements.

How It Works

  • Tetrabenazine reversibly inhibits the vesicular monoamine transporter 2 (VMAT2) located on presynaptic neuronal vesicles. By blocking VMAT2, it prevents the uptake of dopamine, serotonin, norepinephrine and other monoamines into synaptic vesicles, leading to reduced cytoplasmic storage and subsequent depletion of these neurotransmitters in the central nervous system. The resulting decrease in dopaminergic transmission dampens the hyperkinetic activity that underlies chorea and dyskinetic movements.

Side Effects

Tetrabenazine may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Nausea
  • Fatigue
  • Somnolence
  • Dizziness
  • Depression
  • Weight loss

Serious or Rare Side Effects

  • Severe depression or suicidal ideation
  • QT interval prolongation leading to arrhythmia
  • Neuroleptic malignant‑like syndrome
  • Parkinsonism
  • Hepatic toxicity
  • Agranulocytosis

Precautions & Warnings

  • When prescribing tetrabenazine, clinicians should observe several safety considerations.
  • Monitor for depression: assess mood regularly and intervene promptly if worsening occurs.
  • Assess cardiac function: obtain baseline ECG and monitor QT interval during therapy.
  • Avoid abrupt discontinuation: taper dose under medical supervision to prevent withdrawal phenomena.
  • Use caution in hepatic impairment: dose adjustment may be required based on liver function.
  • Avoid concomitant MAO inhibitors: risk of hypertensive crisis and serotonin syndrome.
  • Store at ambient temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Tetrabenazine interacts with several drug classes; awareness of these interactions helps prevent adverse events.

Major Interactions (Avoid)

  • Concomitant MAO inhibitors: may cause hypertensive crisis.
  • Strong CYP2D6 inhibitors (e.g., paroxetine, fluoxetine): increase tetrabenazine plasma levels, raising toxicity risk.
  • QT‑prolonging agents (e.g., quinidine, sotalol): additive risk of cardiac arrhythmias.

Moderate Interactions (Monitor Closely)

  • Antidepressants (SSRIs, SNRIs): may enhance serotonergic effects.
  • Antipsychotics (especially dopamine antagonists): may potentiate motor side effects.
  • Other dopaminergic agents (e.g., levodopa): may reduce therapeutic efficacy.

Frequently Asked Questions

Motetis contains tetrabenazine, which is prescribed to manage hyperkinetic movement disorders. It is approved for reducing chorea in Huntington's disease and for alleviating involuntary movements associated with tardive dyskinesia in adult patients.

Tetrabenazine reversibly blocks the vesicular monoamine transporter 2 (VMAT2). This inhibition prevents dopamine and other monoamines from being stored in neuronal vesicles, leading to lower levels of these neurotransmitters in the brain and consequently dampening excessive motor activity.

The dosage of Motetis is individualized. A qualified prescriber determines the appropriate starting dose and titration schedule based on the patient’s clinical condition, response, and tolerability, following local prescribing guidelines.

Safety data for tetrabenazine in pregnancy and lactation are limited. The drug should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by the treating physician.

To request Motetis, submit an enquiry on the product page at gnhindia.com indicating 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.

The primary alternative is deutetrabenazine, a deuterated form of tetrabenazine that offers a longer half‑life and may require less frequent dosing. Both drugs share the same VMAT2‑inhibiting mechanism, but individual tolerability and dosing convenience can differ, so clinicians choose based on patient response and safety profile.

Motetis should be stored at ambient temperature, below 25 °C. Keep the product in its original packaging, protect it from moisture and direct light, and ensure the container is tightly closed to maintain stability.

Motetis is taken orally. The tablets should be swallowed whole with water and may be taken with or without food, as directed by the prescribing physician.

Serious risks include severe depression or suicidal thoughts, QT interval prolongation that can lead to cardiac arrhythmias, and rare neuroleptic malignant‑like syndrome. Patients should be monitored closely for mood changes, cardiac symptoms and any signs of systemic toxicity.

Motetis is contraindicated in patients with a history of severe depression or suicidal behavior, those with known QT prolongation, and individuals currently taking monoamine oxidase inhibitors. Caution is also advised for patients with significant hepatic impairment or uncontrolled cardiac disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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