Literature DB >> 1964678

High versus low dose granisetron, a selective 5HT3 antagonist, for the prevention of chemotherapy-induced nausea and vomiting.

H C Falkson1, C I Falkson, G Falkson.   

Abstract

Fifty six patients, with histologically confirmed cancer, who received highly emetogenic chemotherapy, were entered on a randomized double blind, low versus high dose, study of granisetron, a 5HT3 receptor antagonist. A single dose of intravenous granisetron protected the majority of patients from nausea and vomiting, 160 micrograms/kg was more effective than 40 micrograms/kg with no more side effects. Additional doses of granisetron conferred added benefit to patients who experienced breakthrough symptoms. Granisetron at a dose range of 40-240 micrograms/kg over a 24 hour period was well tolerated with the only side effect being mild headache.

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Year:  1990        PMID: 1964678     DOI: 10.1007/bf00198602

Source DB:  PubMed          Journal:  Invest New Drugs        ISSN: 0167-6997            Impact factor:   3.850


  6 in total

1.  A phase I study of a new 5HT3-receptor antagonist, BRL43694A, an agent for the prevention of chemotherapy-induced nausea and vomiting.

Authors:  G Falkson; A J van Zyl
Journal:  Cancer Chemother Pharmacol       Date:  1989       Impact factor: 3.333

2.  A pharmacokinetic study of granisetron (BRL 43694A), a selective 5-HT3 receptor antagonist: correlation with anti-emetic response.

Authors:  J Carmichael; B M Cantwell; C M Edwards; B D Zussman; S Thompson; W G Rapeport; A L Harris
Journal:  Cancer Chemother Pharmacol       Date:  1989       Impact factor: 3.333

3.  Blockade of neuronal tryptamine receptors by metoclopramide.

Authors:  J R Fozard; A T Mobarok ALI
Journal:  Eur J Pharmacol       Date:  1978-05-01       Impact factor: 4.432

4.  Inhibition of cisplatin-induced vomiting by selective 5-hydroxytryptamine M-receptor antagonism.

Authors:  W D Miner; G J Sanger
Journal:  Br J Pharmacol       Date:  1986-07       Impact factor: 8.739

5.  GR 38032F (GR-C507/75): a novel compound effective in the prevention of acute cisplatin-induced emesis.

Authors:  P J Hesketh; W K Murphy; E P Lester; D R Gandara; A Khojasteh; E Tapazoglou; G P Sartiano; D R White; K Werner; J M Chubb
Journal:  J Clin Oncol       Date:  1989-06       Impact factor: 44.544

6.  The efficacy and safety of GR38032F in the prophylaxis of ifosfamide-induced nausea and vomiting.

Authors:  J A Green; S W Watkin; P Hammond; J Griggs; T Challoner
Journal:  Cancer Chemother Pharmacol       Date:  1989       Impact factor: 3.333

  6 in total
  2 in total

Review 1.  Granisetron. A review of its pharmacological properties and therapeutic use as an antiemetic.

Authors:  G L Plosker; K L Goa
Journal:  Drugs       Date:  1991-11       Impact factor: 9.546

Review 2.  Volunteer models for predicting antiemetic activity of 5-HT3-receptor antagonists.

Authors:  N A Minton
Journal:  Br J Clin Pharmacol       Date:  1994-06       Impact factor: 4.335

  2 in total

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