Product image of Ketilept Prolong (Quetiapine Fumarate) supplied by GNH India

Ketilept Prolong

Active Ingredient:
Quetiapine Fumarate
Origin:
EU

Ketilept Prolong (Quetiapine Fumarate)

Quetiapine fumarate, the active ingredient in Ketilept Prolong, is an atypical antipsychotic presented as a tablet for oral use, marketed in the European Union. It is indicated for the treatment of schizophrenia, management of manic episodes in bipolar disorder, and as an adjunct therapy for major depressive disorder in adult patients.

GNH India supplies Ketilept Prolong 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

Egis Pharmaceuticals Plc

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Indications & Clinical Uses

Quetiapine fumarate is an atypical antipsychotic that modulates neurotransmitter activity in psychotic and mood disorders.

  • Schizophrenia: reduces delusions, hallucinations and other positive psychotic symptoms.
  • Bipolar disorder (manic episodes): stabilises mood and diminishes the severity of manic swings.
  • Major depressive disorder (adjunct): enhances the therapeutic response when added to standard antidepressant regimens.

How It Works

  • Quetiapine fumarate acts as an antagonist at serotonin 5‑HT2A, dopamine D2, histamine H1 and adrenergic α1 receptors. By blocking D2 receptors it reduces dopaminergic hyperactivity linked to psychosis, while 5‑HT2A antagonism improves mood and cognition. Additional antihistaminic and anti‑adrenergic activity contributes to its sedative and anxiolytic properties, resulting in overall modulation of neurotransmission across multiple pathways.

Side Effects

Quetiapine fumarate may be associated with a range of adverse reactions, varying in frequency and severity.

Common Side Effects

  • Drowsiness: feeling of sleepiness or reduced alertness.
  • Dry mouth: decreased salivation leading to oral discomfort.
  • Constipation: infrequent bowel movements or hard stools.
  • Weight gain: increase in body weight over time.
  • Orthostatic hypotension: drop in blood pressure upon standing causing dizziness.
  • Elevated cholesterol: rise in blood lipid levels.

Serious or Rare Side Effects

  • Neuroleptic malignant syndrome: rare but life‑threatening reaction with fever and muscle rigidity.
  • Agranulocytosis: severe reduction in white blood cells increasing infection risk.
  • Tardive dyskinesia: persistent involuntary movements, especially of the face.
  • Suicidal thoughts: emergence or worsening of suicidal ideation.
  • Severe allergic reaction: rash, swelling, or anaphylaxis.

Precautions & Warnings

When prescribing quetiapine fumarate, clinicians should consider several precautionary measures to ensure safe use.

  • Dose titration: start low and increase gradually to minimise side‑effects.
  • Cardiovascular monitoring: assess blood pressure and heart rate, especially for orthostatic changes.
  • Metabolic screening: regularly check weight, glucose and lipid profiles.
  • Psychiatric assessment: monitor for worsening depression or emergence of suicidal thoughts.
  • Pregnancy and lactation: avoid use unless benefits outweigh potential risks, as safety data are limited.
  • Store at ambient temperature: keep below 25 °C in the original container, protect from moisture and light.

Avoid Interactions

Quetiapine fumarate can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • CYP3A4 inhibitors: strong inhibitors such as ketoconazole may increase quetiapine levels, raising toxicity risk.
  • CNS depressants: concurrent use with alcohol, benzodiazepines or opioids can enhance sedation and respiratory depression.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers: agents like rifampin may lower quetiapine concentrations, reducing effectiveness.
  • Antihypertensives: additive blood‑pressure lowering may cause pronounced hypotension.
  • Anticholinergic drugs: may exacerbate dry mouth and constipation.
  • Antidepressants (e.g., SSRIs): monitor for additive serotonergic effects.

Frequently Asked Questions

Ketilept Prolong contains quetiapine fumarate and is prescribed for the management of schizophrenia, for controlling manic episodes in bipolar disorder, and as an adjunctive treatment to improve response in major depressive disorder when used together with standard antidepressants.

Quetiapine fumarate works by blocking several neurotransmitter receptors, chiefly serotonin 5‑HT2A and dopamine D2, as well as histamine H1 and adrenergic α1 receptors. This receptor antagonism reduces dopaminergic over‑activity linked to psychosis and modulates serotonergic pathways to stabilise mood and alleviate depressive symptoms.

The appropriate dose of Ketilept Prolong is determined individually by a qualified prescriber based on the patient’s condition, response, and tolerability. Clinicians consider factors such as diagnosis, severity, age and concomitant therapies when establishing the dosing regimen.

Safety data for quetiapine fumarate in pregnancy and lactation are limited. The drug 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 the treating physician.

To order Ketilept Prolong, 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.

Ketilept Prolong (quetiapine) shares the broad receptor profile of atypical antipsychotics but is distinguished by its relatively strong antihistaminic and anti‑adrenergic activity, which can lead to more pronounced sedation and orthostatic effects compared with agents such as risperidone or olanzapine. Efficacy for psychosis and mood stabilization is comparable, while side‑effect profiles differ.

Store Ketilept Prolong at ambient temperature, preferably below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight and excessive heat. Ensure the container is tightly closed to maintain tablet integrity until the expiry date.

Ketilept Prolong is taken orally. Tablets should be swallowed whole with a glass of water and may be taken with or without food, as directed by the prescriber. Patients should follow the dosing schedule provided and not split or crush tablets unless specifically advised.

Serious risks include neuroleptic malignant syndrome, a rare but life‑threatening condition characterised by high fever, muscle rigidity and autonomic instability, as well as agranulocytosis, severe reduction in white‑blood‑cell count, and the emergence or worsening of suicidal thoughts. Immediate medical attention is required if any of these occur.

Ketilept Prolong is contraindicated in individuals with known hypersensitivity to quetiapine fumarate or any of its excipients. Caution is also advised for patients with uncontrolled cardiovascular disease, severe hepatic impairment, or a history of neuroleptic malignant syndrome. The medication should be avoided in these populations unless a specialist determines that benefits outweigh risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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