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ASCO open access
INTRODUCTION
The goal of this update is to provide
oncologists, other health care practitioners, patients, and caregivers
with recommendations
regarding the use of netupitant and palonosetron
(NEPA). NEPA was approved by the US Food and Drug Administration (FDA)
in
October 2014 for use in the prevention of acute and
delayed nausea and vomiting associated with initial and repeat courses
of chemotherapy. NEPA is administered orally and
consists of a fixed dose of 300 mg of the neurokinin-1 (NK1) receptor antagonist netupitant combined with 0.50 mg of the 5-hydroxytryptamine type 3 (5-HT3) receptor antagonist palonosetron.....
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