Product image of Kwetina (Quetiapine) supplied by GNH India

Kwetina

Active Ingredient:
Quetiapine
Origin:
EU

Kwetina (Quetiapine)

Quetiapine, the active ingredient in Kwetina, is a atypical antipsychotic presented as an oral tablet for oral use. It treats schizophrenia, bipolar disorder (both manic and depressive episodes) and is used as adjunctive therapy for major depressive disorder in adults.

GNH India supplies Kwetina as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Hasco-Lek

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Indications & Clinical Uses

Quetiapine is an atypical antipsychotic that modulates neurotransmitter activity in several psychiatric disorders.

  • Schizophrenia: reduces psychotic symptoms such as hallucinations and delusions.
  • Bipolar disorder (manic episodes): stabilizes mood and diminishes manic symptoms.
  • Bipolar disorder (depressive episodes): alleviates depressive symptoms.
  • Adjunctive treatment of major depressive disorder: enhances the response to antidepressants.

How It Works

  • Quetiapine antagonizes serotonin 5‑HT2A, dopamine D2, histamine H1, and adrenergic α1 receptors, among others. This multi‑receptor blockade modulates dopaminergic and serotonergic neurotransmission, leading to reduced psychotic activity, mood stabilization, and augmentation of antidepressant effects.

Side Effects

Quetiapine may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Dizziness
  • Somnolence
  • Dry mouth
  • Constipation
  • Weight gain
  • Orthostatic hypotension

Serious or Rare Side Effects

  • Agranulocytosis
  • Neuroleptic malignant syndrome
  • Tardive dyskinesia
  • Severe hypotension
  • Suicidal thoughts or behaviors
  • Myocarditis or pericarditis

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety aspects.

  • Cardiovascular assessment: monitor blood pressure and heart rate, especially in patients with pre‑existing hypertension.
  • Hepatic function: evaluate liver enzymes and adjust dose in severe impairment.
  • Psychiatric history: watch for worsening depression or emergent suicidality.
  • Age considerations: start low and titrate cautiously in elderly patients.
  • Discontinuation: avoid abrupt cessation; taper under medical supervision.
  • Store at ambient temperature: keep in the original pack, protect from moisture and light.

Avoid Interactions

Quetiapine interacts with several drug classes that may require dose adjustment or avoidance.

Major Interactions (Avoid)

  • CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): increase quetiapine plasma levels.
  • CYP3A4 inducers (e.g., rifampin, carbamazepine): reduce therapeutic effect.
  • CNS depressants (alcohol, benzodiazepines): additive sedation and respiratory depression.

Moderate Interactions (Monitor Closely)

  • Antidepressants (SSRIs, SNRIs): potential for serotonin syndrome.
  • Other antipsychotics (haloperidol): increased risk of QT prolongation.
  • Antihypertensives: may cause excessive hypotension.

Frequently Asked Questions

Kwetina contains quetiapine, an atypical antipsychotic indicated for treatment of schizophrenia, management of manic and depressive episodes in bipolar disorder, and as an adjunct to antidepressants in major depressive disorder. It is prescribed by qualified healthcare professionals for adult patients requiring symptom control in these psychiatric conditions.

Quetiapine acts as an antagonist at several neurotransmitter receptors, notably serotonin 5‑HT2A and dopamine D2 receptors, while also blocking histamine H1, adrenergic α1 and other receptors. This receptor profile modulates dopaminergic and serotonergic pathways, reducing psychotic symptoms, stabilizing mood, and enhancing antidepressant effects.

The appropriate dose of Kwetina is determined individually by the prescribing clinician based on the specific indication, patient age, response, and tolerability. Dosage may be started low and titrated upward, but exact amounts and schedules should be obtained from the treating physician’s prescription.

Quetiapine is classified as pregnancy category B1 in the EU, indicating no evidence of fetal risk in animal studies, but human data are limited. It should only be used during pregnancy or lactation if the potential benefit outweighs the risk, and under close medical supervision.

To request Kwetina, 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.

Compared with older typical antipsychotics, quetiapine has a broader receptor profile that often results in lower rates of extrapyramidal symptoms but may cause more sedation and metabolic effects. Relative to other atypicals such as risperidone or olanzapine, its efficacy in psychosis is comparable, while its side‑effect profile differs, influencing clinician choice.

Kwetina should be stored at ambient temperature, below 25 °C, in its original packaging to protect from moisture and light. Keep the product out of reach of children and do not use if the packaging is damaged or the tablet appears discolored.

Kwetina is taken orally, usually with or without food, as directed by the prescribing physician. Tablets should be swallowed whole with a glass of water and not chewed or crushed, unless a specific formulation permits it. Consistent timing each day helps maintain stable drug levels.

The most serious adverse reactions to quetiapine include neuroleptic malignant syndrome, agranulocytosis, severe hypotension, tardive dyskinesia, and suicidal thoughts, particularly when initiating therapy or adjusting dose. Patients should be monitored closely for these events, and any concerning symptoms require immediate medical attention.

Kwetina is contraindicated in patients with known hypersensitivity to quetiapine or any of its excipients. It should be used with caution, or avoided, in individuals with uncontrolled cardiovascular disease, severe hepatic impairment, or a history of neuroleptic malignant syndrome. Pregnant or breastfeeding women should only use it when clearly indicated by a healthcare professional.

Published by

GNH India Pharmaceuticals Limited

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Last updated:

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