Adverse Drug Reaction Retrospective analysis of 82 cases of.docVIP

Adverse Drug Reaction Retrospective analysis of 82 cases of.doc

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 PAGE \* MERGEFORMAT 7 Adverse Drug Reaction Retrospective analysis of 82 cases of [Abstract] Objective: To understand the clinical treatment of adverse drug reactions (ADR) occurrence and triggered by relevant factors. Methods: Descriptive study method in January 2006 ~ December 2007 report of clinical use of drugs classified 82 cases of ADR statistical analysis. Results: The proportion of elderly patients in ADR was significantly higher than other age groups. ADR to a maximum of skin reactions, including rash and pruritus of various common. Conclusion: Only by strengthening the ADR monitoring and reporting, keep abreast of drugs that may exist in a variety of adverse reactions, careful medication, in order to avoid or reduce the ADR duplication, improve rational drug use levels and to protect patient safety of drug use. [Keywords:] of adverse drug reaction; Analysis Since the 20th century, 60 years shocked the world’s ‘reaction to stop the event’ cause for concern in 2006 ‘Houttuynia injection is disabled events’, adverse drug reactions harm a human again sounded the alarm to strengthen ADR monitoring has become a national drug an important regulatory role, this article in our hospital two years, ADR reports collected from the retrospective analysis in order to increase for the pharmacy to provide early warning of suspicious ADR signals for ADR work in depth, to reduce ADR and ADR caused by medical a waste of resources and to enhance the level of rational drug use for reference. 1 Data and methods 1.1 General Information From 2006 to 2007 by hospital clinicians, pharmacists and nurses, found that reported and reviewed by clinical pharmacists and the hospital ADR panel discussions, initially identified as ADR 82 Li. 1.2 Methods According to ADR monitoring requirements, the report includes patient name, sex, age, national origin, weight, occupation, the original illness, personal hobbies, the performance of the process of adverse reactions suspected

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