Efeitos colaterais da ranitidina aplicada em dose terapêutica em cães saudáveis
Carregando...
Data
2010-02-01
Autores
Cavalcanti, Guilherme Albuquerque de Oliveira
Feliciano, Marcus Antônio Rossi [UNESP]
Silveira, Tatiana
Leite, Carlos Artur Lopes
Araújo, Roberto Baracat
Título da Revista
ISSN da Revista
Título de Volume
Editor
Universidade Federal de Santa Maria (UFSM)
Resumo
O objetivo deste trabalho foi verificar se a dose de ranitidina 2mg kg-1, aplicada via intravenosa, causa êmese ou hipotensão em cães saudáveis. Foram selecionados 10 cães da raça Retriever do Labrador, 10 da raça Beagle e 10 cães sem raça definida, sendo cinco animais de cada sexo. Os animais foram submetidos ao exame clínico e à avaliação da pressão sanguínea antes da aplicação do fármaco e também 10 minutos e quatro horas após a administração deste. Após a aplicação, observou-se que 13,3% dos animais apresentaram-se normais; 6,7% dos cães apresentaram apatia; 50% dos animais apresentaram salivação e 30% apresentaram apatia, salivação, mímica de vômito ou êmese. Não houve diminuição significativa da pressão arterial após a administração do fármaco. Conclui-se que o uso de ranitidina na dose terapêutica, aplicada via intravenosa, pode provocar apatia, salivação, mímica de vômito e êmese.
The purpose of this study was to verify if the ranitidine dosage of 2mg kg-1 by intravenous path causes emesis or hypotension in healthy dogs. They were selected 10 Labrador Retriever, 10 Beagles and 10 mongrel dogs, five animals of each sex. The animals were submitted to clinical examination and blood pressure evaluation before ranitidine administration and also 10 minutes and 4 hours after administration of it. After administration was observed that 13.3% of the animals presented normal; 6.7% of the dogs presented apathy; 50% of the animals presented salivation and 30% presented apathy, salivation, emesis mimic or emesis. There was no significative arterial blood pressure decrease after ranitidine administration. It was concluded that ranitidine useful in therapeutic dosage by intravenous path may provoke apathy, salivation, emesis mimic and emesis.
The purpose of this study was to verify if the ranitidine dosage of 2mg kg-1 by intravenous path causes emesis or hypotension in healthy dogs. They were selected 10 Labrador Retriever, 10 Beagles and 10 mongrel dogs, five animals of each sex. The animals were submitted to clinical examination and blood pressure evaluation before ranitidine administration and also 10 minutes and 4 hours after administration of it. After administration was observed that 13.3% of the animals presented normal; 6.7% of the dogs presented apathy; 50% of the animals presented salivation and 30% presented apathy, salivation, emesis mimic or emesis. There was no significative arterial blood pressure decrease after ranitidine administration. It was concluded that ranitidine useful in therapeutic dosage by intravenous path may provoke apathy, salivation, emesis mimic and emesis.
Descrição
Palavras-chave
ranitidina, caninos, efeitos indesejados, vômito, ranitidine, canines, undesired effects, emesis
Como citar
Ciência Rural. Universidade Federal de Santa Maria (UFSM), v. 40, n. 2, p. 326-329, 2010.