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M

M. Namjoshi

Researcher at Eli Lilly and Company

Publications -  18
Citations -  715

M. Namjoshi is an academic researcher from Eli Lilly and Company. The author has contributed to research in topics: Olanzapine & Bipolar disorder. The author has an hindex of 10, co-authored 17 publications receiving 704 citations. Previous affiliations of M. Namjoshi include Harvard University.

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A 12-week, double-blind comparison of olanzapine vs haloperidol in the treatment of acute mania.

TL;DR: The data suggest that olanzapine does not differ from haloperidol in achieving overall remission of bipolar mania, however, hal operidol carries a higher rate of extrapyramidal symptoms, whereas olanZapine is associated with weight gain.
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Long-term olanzapine therapy in the treatment of bipolar I disorder: an open-label continuation phase study

TL;DR: During up to 1 year of olanzapine therapy, either as monotherapy or in combination with lithium and/or fluoxetine, patients with bipolar disorder demonstrated significant improvement in mania and depression symptoms with a favorable safety profile.
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A review of the health-related quality of life literature in bipolar disorder

TL;DR: In the absence of a disease-targeted measure, a combination of the SF-36 and the PGWB is presently recommended as the battery of choice to assess the health-related quality of life of individuals with bipolar disorder.
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Olanzapine versus haloperidol in the treatment of acute mania: clinical outcomes, health-related quality of life and work status.

TL;DR: Compared to haloperidol, olanzapine treatment was comparably effective in the remission of bipolar mania and significantly improved HRQOL and work status in patients with bipolar I disorder.
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Effects of olanzapine alone and olanzapine/fluoxetine combination on health-related quality of life in patients with bipolar depression: secondary analyses of a double-blind, placebo-controlled, randomized clinical trial.

TL;DR: Based on these analyses, patients with bipolar depression receiving olanzapine or OFC for 8 weeks had greater improvement in HRQOL than those receiving placebo, and correlation results support the construct validity of the QLDS.