ASSESSMENT OF THE QUALITY OF “TEMFULGAN” INFUSION SOLUTION BASED ON THE REQUIREMENTS OF THE STATE PHARMACOPOEIA OF UZBEKISTAN AND THE EUROPEAN PHARMACOPOEIA
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Abstract:
This article presents research methods and their results for assessing the compliance of an infusion solution with analgesic-antipyretic action, whose main active substance is paracetamol, with the requirements of the State Pharmacopoeia of the Republic of Uzbekistan and the monographs of the European Pharmacopoeia. Currently, in modern pharmaceutical practice, controlling infusion solutions based on pharmacopoeial requirements is of great importance for ensuring the quality, efficacy, and safety of medicines. During the study, the description, identification, physicochemical parameters, purity, and quantitative composition of the infusion solution were analyzed under laboratory conditions using modern analytical methods. The obtained results showed that the infusion solution fully complies with the requirements of the State Pharmacopoeia of the Republic of Uzbekistan and the monographs of the European Pharmacopoeia. Paracetamol infusion is a widely used medicinal product in healthcare institutions for the treatment of pain and fever. Ensuring the quality and safety of pharmaceutical products is essential for protecting public health. Therefore, it is necessary to study the compliance of the quality of these pharmaceutical products in the pharmaceutical market of Uzbekistan with international standards and guidelines [1].
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