Yellow coloured, circular 8. Olanzapine is effective in maintaining the clinical improvement during continuation therapy in patients who have shown an initial treatment response.
In patients whose manic episode has responded to olanzapine treatment, olanzapine is indicated for the prevention of recurrence in patients with bipolar disorder see section 5. The starting dose is 15 mg as a single daily dose in monotherapy or 10 mg daily in combination therapy see section 5. Preventing recurrence in olanzapine 10 mg tablet 70 mg disorder: Olanzapine 10 mg tablet 70 mg patients who have been receiving olanzapine for treatment of manic episode, continue therapy for preventing recurrence at the same dose.
Click at this page a olanzapine 10 mg tablet 70 mg manic, mixed, or depressive episode occurs, olanzapine treatment should be continued with dose optimisation as neededwith tablet therapy olanzapine 10 mg tablet 70 mg treat mood symptoms, as clinically indicated.
An increase to a dose greater than the recommended olanzapine 10 mg tablet 70 mg dose is advised only after appropriate clinical reassessment and should generally occur at intervals of not less than 24 hours.
Olanzapine can be given without regards for meals as absorption is not affected by food. Gradual tapering of tablet dose should read article considered when discontinuing olanzapine.
A lower starting dose 5 mg should olanzapine considered for such patients. In cases of moderate hepatic insufficiency cirrhosis, Child-Pugh Class Olanzapine or Seroquel and elderlythe starting dose should be 5 mg and only increased with caution.
The starting dose and dose range need not be routinely altered for non-smokers relative to smokers. The metabolism of olanzapine may be induced by smoking.
Clinical monitoring is recommended and an increase of olanzapine olanzapine 10 mg tablet 70 mg may be considered if necessary see section 4. When more than one factor is present which might result in slower metabolism female gender, geriatric age, non-smoking statusconsideration should be given to decreasing the starting dose. Dose escalation, when indicated, should be conservative in such patients.
Olanzapine is not recommended for use in children and adolescents below 18 years of age due to a lack tablet data on safety and efficacy. A greater magnitude of olanzapine 10 mg tablet 70 mg gain, lipid procardia while breastfeeding prolactin alterations has been reported in short term studies of adolescent patients than in olanzapine 10 mg tablet 70 mg of adult patients see sections 4.
Hypersensitivity to the active substance or to any of the excipients listed in section 6. Patients with known risk of narrow-angle glaucoma. During antipsychotic treatment, improvement in the patient's clinical condition here take several days to olanzapine weeks.
Patients should be closely monitored during this period.
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