A competitive serotonin type 3 receptor antagonist. It is effective in the treatment of nausea and vomiting caused by cytotoxic chemotherapy drugs, including cisplatin, and has reported anxiolytic and neuroleptic properties.
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In the adult patient population:
i) orally administered ondansetron tablets and orally disintegrating tablets (ODT) are indicated for:
- the prevention of nausea and vomiting associated with emetogenic cancer chemotherapy, including high dose (ie. greater than or equal to 50 mg/m2) cisplatin therapy, and radiotherapy, and
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Washington University School of Medicine, St. Louis, Missouri, United States
OHSU Knight Cancer Institute, Portland, Oregon, United States
GSK Investigational Site, Tao Yuan County, Taiwan
Hackensack University Medical Center, Hackensack, New Jersey, United States
University of Rochester Cancer Center, Rochester, New York, United States
CCOP - Southeast Cancer Control Consortium, Winston-Salem, North Carolina, United States
CCOP - Scottsdale Oncology Program, Scottsdale, Arizona, United States
Rapid City Regional Hospital, Rapid City, South Dakota, United States
Altru Health Systems, Grand Forks, North Dakota, United States
Hackensack University Medical Center, Hackensack, New Jersey, United States
University of Rochester Cancer Center, Rochester, New York, United States
MBCCOP - Gulf Coast, Mobile, Alabama, United States
CCOP - Mayo Clinic Scottsdale Oncology Program, Scottsdale, Arizona, United States
CCOP - Central Illinois, Decatur, Illinois, United States
Maisonneuve-Rosemont Hospital, Montreal, Quebec, Canada
Centre Hospitalier Universitaire de Quebec, Quebec City, Quebec, Canada
British Columbia Cancer Agency, Vancouver, British Columbia, Canada
South Bay Treatment Center, Chula Vista, California, United States
John A. Burns School of Medicine, Honolulu, Hawaii, United States
Powell Chemical Dependency Center, Des Moines, Iowa, United States
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