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Introduction: Little is known about the use of psychotropic drugs and alcohol among non-institutionalised elderly adults in Germany. Methods: Using data from the German National Health Interview and Examination Survey, we analysed patterns of current psychotropic drug and alcohol use among male and female survey participants between the ages of 60 and Multivariable regression analysis was used to determine factors associated with alcohol consumption and psychotropic drug use. Results: The overall weighted last-week prevalence was Factors significantly related to psychotropic drug use included female sex, older age, poor health status and polypharmacy. Male sex, smoking, higher social status, better health status and living alone were determinants of alcohol consumption. Conclusions: Compared to other European countries, overall psychotropic drug use among the elderly in Germany is slightly lower, whereas alcohol use as risky drinking and concurrent use of alcohol and psychotropic drugs are highly prevalent. It should be of particular concern to health professionals that people at high risk for psychotropic drug use include the most vulnerable subgroups among the elderly. Year Archive Download PDF. Pharmacopsychiatry ; 41 6 : DOI: Further Information Publication History received Also available at. PubMed Google Scholar. Crossref PubMed Google Scholar.

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A prerequisite for the permit is that the establishments comply with the internationally recognized rules of good manufacturing practice or good distribution practice. The permit is limited in time and can be extended again upon application by the company, provided that the requirements are met. Establishments must submit a written application for a permit to the Office of Public Health in the following cases:. Applications for renewal of permits shall be submitted at least 6 months prior to the expiration date of the permit. Manufacturing facilities are generally reviewed every two years for compliance with GMP rules. Wholesale facilities are inspected every two to four years for compliance with GDP rules, depending on the scope of the permit. Public pharmacies or drugstores can manufacture medicines according to their own formula in small quantities. The preparations are not subject to licensing, but must be reported to the Office of Public Health. The Office of Public Health receives these notifications, verifies the marketability of the medicines and issues a confirmation. Last updated: Responsible for content: Liechtenstein National Administration. Automatically translated by DeepL. Production and wholesale. Process of the authorization procedure Establishments must submit a written application for a permit to the Office of Public Health in the following cases: before commencing an activity requiring a permit when information in an existing permit is changed when requesting renewal of an expiring permit Applications for renewal of permits shall be submitted at least 6 months prior to the expiration date of the permit. The subsequent course of the licensing procedure is as follows: On receipt, the Office of Public Health reviews the application and contacts the applicant. Thereafter, an inspection is conducted to determine whether the requirements for a permit have been met. If the requirements are met and there is an application from the Regional Office Zurich to the Office of Health, the Office will issue a temporary permit. Production in small quantities Public pharmacies or drugstores can manufacture medicines according to their own formula in small quantities. Contact persons Dr. Print Share Facebook Twitter E-mail.

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