Prescription Required.
Is the active ingredient in medications like zyprexa.
Treatment of schizophrenia in adults and adolescents (1317 years old)
Treatment of acute manic episodes associated with bipolar I disorder in adults
Maintenance treatment of bipolar I disorder to prevent recurrence of manic or depressive episodes in adults
Tolaz La 405mg Inj (Olanzapine) is an atypical antipsychotic that works by blocking dopamine and serotonin receptors in the brain. This helps to reduce the symptoms of psychosis, mania, and depression.
Store at room temperature away from moisture and heat. Keep out of reach of children.
Dosage is determined by a doctor and varies depending on the condition being treated and individual patient factors.
It is typically taken orally, once daily, with or without food.
Do not stop taking Olanzapine abruptly without consulting your doctor.
Follow your doctor's prescription instructions carefully.
Extrapyramidal symptoms (EPS) such as tremor, rigidity, akathisia (restlessness)
Tardive dyskinesia (TD) (involuntary movements, particularly of the face and tongue)
Weight gain
Increased blood sugar levels
Increased cholesterol levels
Somnolence (sleepiness)
Dizziness
Dry mouth
Constipation
Blurred vision
Avoid alcohol consumption as it can increase the risk of sedation and other side effects.
Avoid driving or operating machinery until you know how Olanzapine affects you. It may cause drowsiness or dizziness.
Inform your doctor if you are pregnant, plan to become pregnant, or are breastfeeding. Olanzapine may pass into breast milk and may pose risks to the infant.
Use in children and adolescents is only indicated for specific conditions and should be under close medical supervision.
Dose adjustment may be necessary in patients with kidney impairment.
Dose adjustment may be necessary in patients with liver impairment.
Your doctor or pharmacist
The official prescribing information (package insert) for Olanzapine.
Reputable medical websites such as the National Institutes of Health (NIH) or the Food and Drug Administration (FDA).
