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If a patient develops signs and symptoms indicative of NMS, or presents with unexplained high fever without additional clinical manifestations of NMS, all antipsychotic medicines, including olanzapine must be discontinued. In some cases, a prior increase in body weight has been reported, which may be a predisposing factor. Weight should be monitored regularly, e. Undesirable alterations in lipids have been observed in https://play.google.com olanzapine-treated patients in placebo-controlled clinical trials see section 4. Transient, asymptomatic elevations of hepatic aminotransferases, ALT, AST have been seen commonly, especially in early treatment. In cases where hepatitis including hepatocellular, cholestatic or mixed liver injury has been diagnosed, olanzapine treatment should be discontinued.
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Co-administered medicinal product and dosing regimen. Co-administration with products containing glecaprevir or pibrentasvir is contraindicated see section 4. In cases where co-administration with atorvastatin is necessary, do not exceed 10 mg atorvastatin daily.
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Olanzapine is an antipsychotic, antimanic, and mood stabilising agent that demonstrates a broad pharmacologic profile across a number of receptor systems. Animal behavioural studies with olanzapine indicated 5HT, dopamine, and cholinergic antagonism, consistent with the receptor-binding profile.
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