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 an adjunct in major depressive disorder, helping to balance neurotransmitter activity in affected patients through modulation of serotonin and dopamine pathways.

GNH India supplies Kventiax Sr as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring quality and regulatory compliance across all markets with reliable logistics and documentation support.

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Quetiapine is an atypical antipsychotic that modulates neurotransmission in psychotic and mood disorders.

  • Schizophrenia: reduces hallucinations, delusions and other psychotic symptoms, improving functional outcomes.
  • Bipolar disorder: stabilizes mood during manic and depressive phases, decreasing episode frequency.
  • Major depressive disorder (adjunct therapy): enhances response to standard antidepressants when added to the regimen.
  • Psychotic depression: alleviates psychotic features accompanying depressive episodes.

How It Works

  • Quetiapine acts as an antagonist at serotonin 5‑HT₂A, dopamine D₂, histamine H₁, and adrenergic α₁ receptors, with additional activity at other neurotransmitter sites. By blocking 5‑HT₂A and D₂ receptors, it reduces dopaminergic and serotonergic over‑activity implicated in psychosis and mood instability, while its antihistaminic and anti‑adrenergic effects contribute to its sedative and anxiolytic properties.

Side Effects

Quetiapine may cause 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.

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, increasing infection risk.

Precautions & Warnings

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

  • Assess cardiovascular status: monitor blood pressure and heart rate, especially in patients prone to orthostatic hypotension.
  • Evaluate metabolic risk: screen for diabetes, lipid abnormalities, and weight changes before and during therapy.
  • Review psychiatric history: monitor for emergence of suicidal thoughts or worsening depression.
  • Consider hepatic and renal function: adjust use in patients with significant liver or kidney impairment.
  • Avoid abrupt discontinuation: taper dose gradually to reduce risk of withdrawal symptoms.
  • Store at ambient temperature: keep tablets in original container, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase quetiapine plasma levels, risking toxicity.
  • CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce quetiapine concentrations, diminishing efficacy.
  • CNS depressants (e.g., benzodiazepines, opioids): additive sedation and respiratory depression.

Moderate Interactions (Monitor Closely)

  • Antihypertensives: enhanced hypotensive effect when combined with quetiapine.
  • Anticholinergic agents: may exacerbate dry mouth and constipation.
  • Antidepressants (e.g., SSRIs, SNRIs): potential for increased serotonergic activity and QT prolongation.

Frequently Asked Questions

Kventiax Sr contains quetiapine, an atypical antipsychotic indicated for the treatment of schizophrenia, bipolar disorder, and as an adjunctive therapy in major depressive disorder. It helps control psychotic symptoms, stabilise mood swings, and improve response to antidepressants in appropriate patients.

Quetiapine works by blocking several neurotransmitter receptors, chiefly serotonin 5‑HT₂A and dopamine D₂ receptors, while also antagonising histamine H₁ and adrenergic α₁ receptors. This receptor profile reduces excessive dopaminergic and serotonergic activity, which underlies psychotic and mood‑related symptoms.

The specific dose of Kventiax Sr is determined by the prescribing clinician based on the individual’s diagnosis, severity of symptoms, age, renal and hepatic function, and response to therapy. Only a qualified healthcare professional should decide the appropriate dosing regimen.

Safety data for quetiapine in pregnancy and lactation are limited. The medication 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 risks and alternatives with their healthcare provider.

To order Kventiax Sr, 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) belongs to the atypical antipsychotic class, which differs from typical antipsychotics by offering a lower risk of extrapyramidal symptoms but a higher propensity for metabolic side effects. Compared with other atypicals such as risperidone or olanzapine, quetiapine often provides stronger sedative effects and is frequently chosen for its adjunctive role in depression.

Kventiax Sr tablets should be stored at ambient temperature, below 25 °C, in the original container to protect them from moisture, light and humidity. Keep the product out of reach of children and do not use if the packaging is damaged or the tablets appear discoloured.

Kventiax Sr is taken orally, usually with or without food, as directed by the prescribing clinician. The tablets are swallowed whole with a glass of water. Patients should follow the prescribed schedule and not alter the dose without medical advice.

Serious risks include neuroleptic malignant syndrome, a rare but life‑threatening condition characterized by high fever, muscle rigidity and autonomic instability; tardive dyskinesia, which involves persistent involuntary movements; agranulocytosis, a severe drop in white blood cells; and the emergence or worsening of suicidal thoughts, especially during early treatment.

Kventiax Sr should be avoided in individuals with known hypersensitivity to quetiapine or any of its excipients. Caution is advised for patients with uncontrolled cardiovascular disease, severe hepatic impairment, or a history of neuroleptic malignant syndrome. It is also contraindicated in patients currently receiving monoamine oxidase inhibitors.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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