Product image of Kventiax Sr (Quetiapine) supplied by GNH India

Kventiax Sr

Active Ingredient:
Quetiapine
Origin:
EU

Kventiax Sr (Quetiapine)

Quetiapine, the active ingredient in Kventiax Sr, is an atypical antipsychotic presented as an oral dosage form for oral use. It is prescribed for the management of schizophrenia, bipolar disorder and as adjunct therapy in major depressive disorder in adult patients.

GNH India supplies Kventiax Sr as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Quetiapine is used in several psychiatric conditions that involve dysregulation of dopamine and serotonin pathways.

  • Schizophrenia: reduces psychotic symptoms such as hallucinations and delusions.
  • Bipolar disorder (manic and depressive episodes): stabilises mood and prevents relapse of manic or depressive episodes.
  • Major depressive disorder (adjunct therapy): enhances antidepressant response when added to standard treatment.

How It Works

  • Quetiapine acts as an antagonist at dopamine D2 receptors and serotonin 5‑HT2A/2C receptors, while also blocking histamine H1 and adrenergic α1 receptors. It exhibits partial agonist activity at 5‑HT1A receptors, resulting in modulation of dopaminergic and serotonergic neurotransmission that underlies its antipsychotic and mood‑stabilising effects.

Side Effects

Quetiapine may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Drowsiness: feeling unusually sleepy or fatigued.
  • Dry mouth: reduced salivation leading to discomfort.
  • Constipation: infrequent or difficult bowel movements.
  • Weight gain: increase in body weight over time.
  • Orthostatic hypotension: drop in blood pressure upon standing.
  • Dizziness: sensation of light‑headedness.

Serious or Rare Side Effects

  • Neuroleptic malignant syndrome: rare but life‑threatening reaction with fever and muscle rigidity.
  • Tardive dyskinesia: persistent involuntary movements, especially of the face.
  • Agranulocytosis: severe reduction in white blood cells.
  • Seizures: increased risk of convulsive episodes.
  • Suicidal thoughts: emergence or worsening of suicidal ideation.

Precautions & Warnings

When prescribing quetiapine, clinicians should consider several safety aspects.

  • Cardiovascular monitoring: assess for orthostatic hypotension and ECG changes.
  • Metabolic assessment: monitor weight, glucose, and lipid levels regularly.
  • CNS depression: caution when combined with other sedatives or alcohol.
  • Pregnancy and lactation: evaluate risk‑benefit as safety data are limited.
  • Elderly patients: start at low doses and watch for increased sensitivity to side effects.
  • Store at ambient temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Quetiapine interacts with several drug classes that may alter its efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase quetiapine plasma levels.
  • CNS depressants (e.g., benzodiazepines, opioids): can enhance sedation and respiratory depression.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., carbamazepine, rifampin): may reduce quetiapine concentrations.
  • Antihypertensives: additive effect on blood pressure lowering.
  • Anticholinergic agents: may worsen dry mouth and constipation.

Frequently Asked Questions

Kventiax Sr contains quetiapine, which is indicated for the treatment of schizophrenia, bipolar disorder (both manic and depressive phases), and as an adjunctive therapy for major depressive disorder in adult patients.

Quetiapine blocks dopamine D2 and serotonin 5‑HT2A/2C receptors while partially stimulating 5‑HT1A receptors. This combined antagonism and partial agonism modulates neurotransmitter activity, helping to reduce psychotic symptoms and stabilise mood.

The appropriate dose of Kventiax Sr is determined by the prescribing clinician based on the individual’s diagnosis, severity of symptoms, response to therapy and tolerability. Dosing regimens are not standardized and should follow the prescriber’s instructions.

Safety data for quetiapine in pregnancy and lactation are limited. Clinicians must weigh potential benefits against possible risks to the fetus or infant, and use the medication only if clearly indicated.

To place an order, 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.

Kventiax Sr (quetiapine) shares the broad receptor profile typical of atypical antipsychotics but is distinguished by its relatively lower affinity for dopamine D2 receptors and higher affinity for histamine H1, which can lead to more pronounced sedation and weight gain compared with some alternatives.

Kventiax Sr should be stored at room temperature, below 25 °C, in its original packaging. Protect the product from moisture, direct sunlight and extreme temperature fluctuations to maintain stability.

Kventiax Sr is taken orally, usually with or without food, as directed by the prescriber. Tablets should be swallowed whole with water and not crushed or chewed unless specifically instructed.

Serious risks include neuroleptic malignant syndrome, tardive dyskinesia, agranulocytosis, seizures, and the emergence or worsening of suicidal thoughts. Patients should be monitored closely for any of these events.

Kventiax Sr is contraindicated in patients with known hypersensitivity to quetiapine or any of its excipients. Caution is also advised for individuals with uncontrolled cardiovascular disease, severe hepatic impairment, or a history of neuroleptic malignant syndrome.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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