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Medication Safety - Research Paper Example

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Institution Instructor Date Medication Safety Turner Rick sought to analyze the issue of drug safety, patient safety, as well as medication safety, with a special attention to recent initiatives and guidelines from FDA. Pharmacotherapy as well as development of drugs is critical components to pharmaceutical medicine…
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Medication Safety
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"Medication Safety"

Drug and medication safety form critical aspects of patient safety and have received great attention in the US in the recent past for the purpose of effective medical management. In particular, FDA has shown special attention in creation of awareness of importance in development of drugs as well as pharmacotherapy. It is committed at expanding as well as governance in processes of development of lifecycle drugs in the US. Its basic purpose is to ensure safety in medicine use (Turner, 4-8; Bollyky, 11). There is a wave of considerable interest for improved patient safety in the US, with great advocacy by such teams as the FDA. Others are Institute of medicine, patient advocacy groups, companies of pharmaceutical and biopharmaceuticals as well as the media to name but least. The article affirms that all drugs have the capacity to cause adverse effects towards the well-being of the general population. It also confirms that all persons are susceptible to harm from poor medication hence the need to have the drug and general medication safety. In defining safety, the report has it that it is the inverse of harm and explains that drug toxicity determine safety; the less the level of toxicity, the higher the levels of safety. The federal law requires that safety be upheld in drug use within the states. However, it is worth noting that safety may not necessarily mean zero risk and as such, all safe drugs depict the acceptable levels of risk. It is critical to carry out the benefit-risk assessment while using medical drugs in order to ascertain the safety and benefits of the drugs as used by the general population. The assessment is done at two basic levels within the medical chain, which are at the public health level as well as at the patient-physician level. The estimation of benefits/ risks compares the estimated good over the estimated harm and as such, the index would be instrumental in explaining the safety levels of the drugs as they apply to the patients and general populations at large. The report highlights some recommended literatures that would be instrumental in enlightening the public on medication safety as a critical tenet in improved health. Among these literatures are the ‘cardiac drug safety’, ‘drug-induced liver injury’ as well as ‘Risk characterization, assessment, Management as well as minimization’. Moreover, the report highlights some initiatives that are relevant in addressing the topic of drug safety. Such initiatives are the 2008 five-year on drug safety in the US, ‘employment of mitigation strategies and risk evaluation’, ‘sentinel initiative’ as well as initiative to ‘safety first/safe use’. In sum therefore, the article has been instrumental in outlining the objectives of FDA especially in the recent past concerning medication and drug safety in the United States. However, just as is the case with all other regulatory bodies and agencies, FDA stands to be challenged and criticized for improving the regulation mandate. Personal opinion In a personal opinion, the FDA has adopted a very critical role in the economy, not just for the purpose of improving the levels of health to the public but also concerning economic performance and development. Monitoring bodies restores and ensures that sanity in such a sensitive sector is upheld at all times and at all costs. Safety in medication presents a critical hurdle in healthcare Read More
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