Product image of Levopraid Per Uso I.M./E.V. (Levosulpiride) supplied by GNH India

Levopraid Per Uso I.M./E.V.

Active Ingredient:
Levosulpiride
Origin:
EU

Levopraid Per Uso I.M./E.V. (Levosulpiride)

Levosulpiride, the active ingredient in Levopraid Per Uso I.M./E.V., is a benzamide derivative (atypical antipsychotic) presented as a sterile injectable solution for intramuscular and intravenous use. It is employed to treat schizophrenia, other psychotic disorders, nausea and vomiting, and gastrointestinal motility disorders in adult patients.

GNH India supplies Levopraid Per Uso I.M./E.V. 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.

Manufacturer / TM Owner

Teofarma S.R.L.

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Indications & Clinical Uses

  • Levosulpiride is used in the management of psychotic and gastrointestinal disorders.
  • Schizophrenia: alleviates positive and negative symptoms, improving thought organization and reducing hallucinations in adult patients.
  • Other psychotic disorders: reduces acute psychotic episodes and stabilizes mood in conditions such as schizoaffective disorder.
  • Nausea and vomiting: controls chemotherapy‑induced or postoperative nausea, providing anti‑emetic relief when administered intravenously.
  • Gastrointestinal motility disorders: enhances gastric emptying and intestinal transit, helping patients with functional dyspepsia or gastroparesis.

How It Works

  • Levosulpiride selectively antagonizes dopamine D2 receptors in the central nervous system, thereby reducing dopaminergic over‑activity that underlies psychotic symptoms. It also exhibits moderate antagonism at D3 and D4 receptors and enhances cholinergic neurotransmission in the gastrointestinal tract, producing a prokinetic effect that facilitates gastric emptying and intestinal motility.

Side Effects

Levosulpiride may cause a range of adverse reactions, varying from mild to serious.

Common Side Effects

  • Drowsiness: increased sleepiness or fatigue, especially after initial doses.
  • Extrapyramidal symptoms: muscle stiffness, tremor, or involuntary movements.
  • Dry mouth: reduced salivation leading to discomfort.
  • Constipation: slowed intestinal transit causing difficulty passing stool.

Serious or Rare Side Effects

  • Neuroleptic malignant syndrome: rare but life‑threatening condition with fever, rigidity, autonomic instability.
  • Tardive dyskinesia: persistent involuntary facial or limb movements that may be irreversible.
  • Severe allergic reactions: anaphylaxis, angioedema, or widespread rash requiring immediate medical attention.

Precautions & Warnings

When prescribing levosulpiride, clinicians should observe several safety considerations.

  • Monitor extrapyramidal symptoms: assess patients regularly for signs of movement disorders.
  • Check prolactin levels: hyperprolactinemia may occur, especially with prolonged therapy.
  • Use caution in cardiovascular disease: may cause hypotension or arrhythmias in susceptible individuals.
  • Avoid in patients with known hypersensitivity: discontinue immediately if allergic reaction develops.
  • Pregnancy and lactation: prescribe only if potential benefit justifies potential risk to fetus or infant.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Levosulpiride can interact with other medicines, affecting its efficacy or safety.

Major Interactions (Avoid)

  • Other dopamine antagonists (e.g., haloperidol): additive risk of extrapyramidal symptoms and hyperprolactinemia.
  • CNS depressants (benzodiazepines, opioids): may enhance sedation and respiratory depression.
  • Anticholinergic agents: can mask early signs of movement disorders.

Moderate Interactions (Monitor Closely)

  • CYP2D6 inhibitors (fluoxetine, paroxetine): may increase levosulpiride plasma concentrations.
  • CYP3A4 inducers (rifampicin, carbamazepine): may reduce drug levels, diminishing therapeutic effect.
  • Diuretics (furosemide): may potentiate hypotensive effects.

Frequently Asked Questions

Levopraid Per Uso I.M./E.V. contains levosulpiride, which is indicated for the treatment of schizophrenia and other psychotic disorders, as well as for controlling nausea and vomiting and for improving gastrointestinal motility in conditions such as gastroparesis.

Levosulpiride works by selectively blocking dopamine D2 receptors in the brain, reducing dopaminergic over‑activity that contributes to psychotic symptoms. It also promotes gastrointestinal motility by enhancing cholinergic activity, helping to accelerate gastric emptying.

The dosage of Levopraid Per Uso I.M./E.V. is determined by the prescribing clinician based on the patient’s condition, severity, and response to therapy. Specific dosing regimens are not provided here and should follow the prescriber’s instructions.

Safety data for levosulpiride in pregnancy and lactation are limited. It should only be used when 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 place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if required) and necessary import documentation.

Compared with typical antipsychotics such as haloperidol, levosulpiride has a lower propensity for causing severe extrapyramidal side effects but still carries a risk of movement disorders. Its additional prokinetic activity makes it useful for gastrointestinal indications, a feature not shared by many other antipsychotic agents.

Levopraid Per Uso I.M./E.V. should be stored at ambient temperature, protected from light and moisture, and kept in its original packaging until use. Do not freeze the product, and ensure the vial is inspected for particulate matter before administration.

The product is supplied as a sterile injectable solution for intramuscular or intravenous injection. Administration is performed by a qualified healthcare professional using aseptic technique, and the dose is adjusted according to the prescriber’s order.

The most serious adverse reactions include neuroleptic malignant syndrome, which is a life‑threatening emergency, tardive dyskinesia, which may be irreversible, and severe allergic reactions such as anaphylaxis. Prompt medical attention is required if any of these events occur.

Levosulpiride is contraindicated in patients with known hypersensitivity to the drug or any benzamide derivative. Caution is also advised for individuals with severe cardiovascular disease, uncontrolled hypertension, or a history of neuroleptic malignant syndrome.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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