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Background. There is currently many over the counter products on the market that exert nutritional or physiological effects on the human body. The differences between dietary supplements and non-prescription drugs are however poorly understood by the average consumer and may thus affect their expectations as to the desired effect produced on the body. Objectives. To evaluate patients’ knowledge and attitudes towards dietary supplements as compared to non-prescription drugs. Materials and Methods. Subjects were 335 patients of the Mazowiecki Voivodeship Hospital in Warsaw, Poland. The data were collected from a face-to-face interview using a single and multiple choice questionnaire with 10 questions on dietary supplements. Statistical analysis used the Chi-square (χ2) test. Results. The majority of respondents were found to be familiar with the term ‘dietary supplements’, but had difficulties in classifying these products into appropriate categories. Over 55% do not consider dietary supplements to be foodstuffs and more than 40% considered such products to be drugs. Most respondents thought that the main purpose of taking dietary supplements is to improve nutrition, but over one third expected them to also treat disease. Over 70% declared taking notice to which category the non-prescription products they bought belongs to ie. whether non-prescription drugs (medicinal products) or dietary supplements. Conclusions. Many patients mistakenly believe that dietary supplements are drugs and can be used to treat disease and health disorders.
Subject and purpose of work: The subject matter of the study is irregularities in the distribution channels of medicinal products, medical devices and foodstuffs for particular nutritional uses. The inversion of distribution on the Polish pharmaceutical market has taken the form of illegal export of medicinal products, becoming one of the main aspects of cross-border crime. The purpose of the study is to identify the causes, present the essence and point to the effects of uncontrolled exports of pharmaceuticals for the Polish medicinal products supply system. Materials and methods: The fulfilment of the article's objective requires the application of the following research methods: literature analysis and criticism, legal document analysis and document examination. The application of these research methods makes it possible to present the results of the analyses and formulate conclusions on the impact of illegal export of medicinal products on the condition of the healthcare system in Poland. Results: When presenting the results of the analyses, it should be noted that so far pharmaceutical market supervision has proven insufficient and defective at every possible level. A tangible manifestation of the inefficiency of the supervision system are State budget losses of PLN 4 billion per year and the absence and deficiencies of the so-called deficit medicines in retail pharmacies, which the Ministry of Health estimates at 386 items. Conclusions: The sine qua non condition for the appropriate operation of the public healthcare system is to ensure effective supervision over the distribution process of medicinal products and adequate control over the entire pharmaceutical market. This cannot be achieved without an effective supervision system. Changing the previous supervision model to the integrated supervision system based on the connection of pharmaceutical supervision subsystems with the tax and labour inspection subsystems will make it possible to effectively counteract illegal exports of medicinal products.
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