Defendant glaxosmithkline llc d b a glaxosmithkline gsk knew as early as 1992 that zofran passed through the placenta and into a developing fetus and presented unreasonable risk of harm to developing babies.
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Known to have hypersensitivitye.ganaphylaxisto ondansetron or any of the components of the formulationsee ADVERSE REACTIONSreceiving concomitant apomorphine due to the risk of profound hypotension and loss of consciousness.
The safety and effectiveness of orally administered ZOFRAN have not been established in pediatric patients for:
Measure the liquid form of ondansetron with a special dose-measuring spoon or cupnot a regular table spoonIf you do not have a dose-measuring deviceask your pharmacist for one.
ZOFRAN ODT orally disintegrating tablets are whiteroundand plano-convex tablets available in the following strengths:
Previous versions of the ondansetron labels included a warning about QT interval prolongationThe FDA added a new warning to avoid the use of ondansetron in patients with congenital long QT syndrome because these patients are at particular risk for developing Torsade.
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