IMPORTANT REQUIREMENTS FOR STUDYING THE GENERAL TOXIC EFFECTS OF PHARMACOLOGICAL SUBSTANCES

Authors

  • Rizakova Diloram Pulatovna Assistant of ASMI

Keywords:

Preclinical toxicological studies, laboratory animals, pharmacological substances, method.

Abstract

 

The article provides an overview of methodological recommendations, rules and guidelines for conducting preclinical studies of the general toxic effects of pharmacological drugs based on international requirements for studies.

References

Astakhova A.V., Lepakhin V.K. Adverse side reactions and drug safety monitoring. – M., 2014.

Belenky M. L. In the book: Elements of quantitative assessment of the pharmacological effect. – L., 2018.

Berezovskaya I.V. Classification of chemical substances according to parameters of acute toxicity for parenteral routes of administration. Chem.-pharm. magazine. – 2013. – T. 37. – No. 3.

Zapadnyuk I.P., Zapadnyuk V.I., Zacharia E.A., Zapadnyuk B.V. Laboratory animals. Breeding, maintenance, use in experiments, 3rd ed., revised. and additional – Kyiv: Vishcha School, 2013.

Published

2024-03-03

How to Cite

Rizakova Diloram Pulatovna. (2024). IMPORTANT REQUIREMENTS FOR STUDYING THE GENERAL TOXIC EFFECTS OF PHARMACOLOGICAL SUBSTANCES. Ethiopian International Journal of Multidisciplinary Research, 11(02), 382–383. Retrieved from https://eijmr.org/index.php/eijmr/article/view/1149