2009
DOI: 10.2165/11200980-000000000-00000
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Palonosetron

Abstract: Palonosetron is a second-generation serotonin 5-HT3 receptor antagonist, with a distinct pharmacological profile that differs from first-generation 5-HT3 receptor antagonists. Intravenous palonosetron is widely indicated for the prevention of chemotherapy-induced nausea and vomiting (CINV) in the acute and delayed phases following moderately emetogenic chemotherapy (MEC) and the prevention of CINV in the acute phase following highly emetogenic chemotherapy (HEC). In the US, oral palonosetron is approved for th… Show more

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Cited by 63 publications
(32 citation statements)
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“…Moreover, pain of pelvic or visceral origin has been suggested as a significant cause of PONV 28. Although palonosetron and ramosetron are both 5-HT3 receptor antagonists, palonosetron is structurally distinct from first-generation drugs and exhibits allosteric binding and positive cooperativity 29. However, whether palonosetron has greater efficacy after abdominal or pelvic surgery is not known and cannot be judged from the present analysis.…”
Section: Discussionmentioning
confidence: 89%
“…Moreover, pain of pelvic or visceral origin has been suggested as a significant cause of PONV 28. Although palonosetron and ramosetron are both 5-HT3 receptor antagonists, palonosetron is structurally distinct from first-generation drugs and exhibits allosteric binding and positive cooperativity 29. However, whether palonosetron has greater efficacy after abdominal or pelvic surgery is not known and cannot be judged from the present analysis.…”
Section: Discussionmentioning
confidence: 89%
“…The 5-HT 3 receptor antagonist palonosetron has a greater binding affinity and longer half-life than other 5-HT 3 receptor antagonist [19]. The unique pharmacokinetics of palonosetron have been associated with clinical outcomes including better prevention of chemotherapy-induced nausea and vomiting compared with other 5-HT 3 drugs [20].…”
Section: Discussionmentioning
confidence: 99%
“…In the US, FDA has already approved for oral formulation of palonosetron for CINV. [20] An effective dose of palonosetron 0.50 mg oral has been favored for the prevention of CINV in patients receiving moderately emetogenic chemotherapy without a side effect disadvantage. Probably, this single dose in high risk patient before anesthesia may prevent PONV.…”
Section: Pharmacokineticsmentioning
confidence: 99%