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.
Having been developed in the 1980s by GlaxoSmithKline and approved by the US FDA since January 1991, ondansetron has demonstrated a long history of use and efficacy. Commonly formulated as oral tablets, orally disintegrating tablets (ODT), and injections, and available as generic products as well, ondansetron continues to see contemporary innovations in its formulation and use, including the development of orally soluble films that are both discreet in administration and less of a burden in comparison to having patients attempt to swallow pills during emesis.
The FDA withdrew its approval for the use of all intravenous drug products containing more than 16 mg of ondansetron hydrochloride in a single dose, due to a high risk of QT prolongation.
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
- the prevention and treatment of postoperative nausea and vomiting
ii) intravenously administered ondansetron injection formulations 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
- the prevention and treatment of postoperative nausea and vomiting
In the pediatric (4-18 years of age) patient population:
i) ondansetron was effective and well tolerated when given to children 4-12 years of age for the treatment of post-chemotherapy induced nausea and vomiting,
ii) ondansetron tablets, ondansetron ODT, ondansetron injection are not indicated for the treatment of children 3 years of age or younger,
iii) ondansetron tablets, ondansetron ODT, ondansetron injection are not indicated for use in any age group of the pediatric population for the treatment of post-radiotherapy induced nausea and vomiting, and
iV) ondansetron tablets, ondansetron ODT, ondansetron injection are not indicated for use in any age group of the pediatric population for the treatment of postoperative nausea and vomiting
In the geriatric (>65 years of age) patient population:
i) efficacy and tolerance of ondansetron were similar to that observed in younger adults for the treatment of post-chemotherapy and radiotherapy-induced nausea and vomiting, and
ii) clinical experience in the use of ondansetron in the prevention and treatment of postoperative nausea and vomiting is limited and is not indicated for use in the geriatric patient population
Clinical Pharmacology Unit, Majeedia Hospital (2nd Floor), New Delhi, India
Clinical Pharmacology Unit, Majeedia Hospital (2nd Floor), New Delhi, India
Visions Clinical Research, Boynton Beach, Florida, United States
CAP Anesthesia (St. Elizabeth's Medical Center), Boston, Massachusetts, United States
University of Pittsburg, Pittsburgh, Pennsylvania, United States
Seoul National University Hospital, Seoul, Korea, Republic of
The Ohio State University Wexner Medical Center, Columbus, Ohio, United States
The Preston Robert Tisch Brain Tumor Center at Duke, Durham, North Carolina, United States
GSK Investigational Site, Austin, Texas, United States
A. I. duPont Hospital for Children, Wilmington, Delaware, United States
Nemours Children's Clinic, Pensacola, Florida, United States
Medical University of South Carolina, Charleston, South Carolina, United States
University of Virginia Health System, Charlottesville, Virginia, United States
Louisiana State University Health Sciences Center, Shreveport, Louisiana, United States
Department of Intensive Care and Anesthesiology, Olsztyn, Poland
Shoals Medical Research, LLC, Sheffield, Alabama, United States
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