Information about Zyprexa.
The conditions and duration of treatment with olanzapine varied greatly and includedin overlapping categoriesopen-label and double-blind phases of studiesinpatients and outpatientsfixed-dose and dose-titration studiesand short-term or longer-term exposureAdverse reactions were assessed by collecting adverse reactionsresults of physical examinationsvital signsweightslaboratory analytesECGschest x-raysand results of ophthalmologic examinations.
Adverse reactions during exposure were obtained by spontaneous report and recorded by clinical investigators using terminology of their own choosingConsequentlyit is not possible to provide a meaningful estimate of the proportion of individuals experiencing adverse reactions without first grouping similar types of reactions into a smaller number of standardized reaction categoriesIn the tables and tabulations that followMedDRA and COSTART Dictionary terminology has been used to classify reported adverse reactions.
There have been no controlled human pregnancy studies on the effects of ZyprexaThe drug can be transferred via human breast milk and potentially harm a babyThereforetalk to your doctor if you are pregnantplanning to become pregnantor are nursing before you take Zyprexa.
Talk to the doctor about the risks and benefits of treatmentespecially when used by teenagersSee also Precautions section.
Zyprexa is usually taken once a dayOlanzapine may be only part of a complete program of treatment that also includes counseling and other psychological support programsFollow your doctor's instructions.
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eli lilly, known in recent years by many for their focus on marketing over science or research, greatly desired and hoped that zyprexa would be a welcome blockbuster for them, which is a medication that exceeds a billion dollars a year in sales as a minimum.