uestion #: 1 Which of the following does a Pharmacy &Therapeutics Committee do? (Select all that apply) A. Educates patients about medications on the formulary used at the hospital B. Dispenses medications that are on the formulary used at the hospital C. Makes decisions on whether a drug should be added to the formulary used at the hospital D. Manages the formulary to be used by physicians, nurses and pharmacists at the hospital Item ID: 1911 / 2 Item Description: Final Exam Pharmacy and Therapeutics
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against the pro side and has factual evidence to back it up, making it a reliable source. Tammaru, T.-M., et al. “Advertising of Medicinal Products to the General Public, Opinions and Attitudes of Customers and Pharmacists.” European Journal of Pharmaceutical Sciences, vol. 32, no. 1, 2007, Elsevier, doi: 10.1016/j.ejps.2007.05.066. Accessed 8 Feb. 2018. Questionnaires were sent out to 100 randomly assigned pharmacists with only 76 responses and a poll was posted and mailed out to the public for a
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I have been impressed immensely by pharmaceutical care and how it is applied in the field of pharmacy. The idea of pharmaceutical care makes so much sense in terms of improving healthcare in the country. The exposure to pharmaceutical care started during becoming a pharmacist. I have attained so much information about it and how it all starts and end with the patient. The goal of pharmaceutical care is aimed at providing optimum health for the population through three main branches. This involves
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The first type of parenteral route of drug administration involves subcutaneous injection, which is given in the fatty layer of tissue under the skin where the hypodermis lies (Bethesda, 2015). The equipment required for this particular method of injection includes gloves, alcohol pads, sterile 2 x 2-inch gauze pads, container for syringe disposal, medication log, syringes, and 25-gauge needles (Bethesda, 2015). 27-gauge needles may be used depending on the amount of medication to be administered
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Germany, 1870- The beginning of the pharmaceutical era came about as a result of apothecaries, dye smiths, and researchers who realized that the combination of those variables contained medical and monetary value. 1890’s- The industry became regulated in Germany and France. “The end of the 19th century includes the production of vaccines against tetanus and diphtheria” 1902- The Biologics Control Act regulated the pharmaceutical industry in the United States, however, it did not regulate the production
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Nonetheless, a significant amount of studies focuses on the controversy of DTCA based upon the potentially greater ratio of risks to benefits. Analyses suggest that the main reason for the controversy surrounding DTCA is its potential influence in increasing the demand for prescription drugs and, subsequently, driving up drug spending. However, most studies conclude that more research is required on DTCA impact, whether negative to positive. Collectively, the literature encourages consumers and pharmacists
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The conventional society cures were utilized for a considerable length of time due to their recuperating properties, and today we are turning out to be more mindful of their effectiveness. Castor oil is regularly prescribed by all encompassing prescription on account of different wellbeing issues, regardless of the fact that routine treatments have neglected to convey beneficial outcomes. Castor oil is known for its advantages on dissemination, and this is the motivation behind why it is utilized
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This paper provides an overview of the modern US generic drug industry evolution after the Hatch-Waxman Act of 1984, considered one of the most significant legislation impacting generic drug approval to the US pharmaceutical market. In the early 1980s, there were very few generic drug products in the US market. Although the Federal Food, Drug, and Cosmetic Act (FD&C Act) made it possible to gain generic drugs approval via the “paper new drug application (NDA)”, it was still difficult for generic
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and the Challenges of the Global Pharmaceutical Industry Case Study Introduction This report is to summarize the results of Pfizer’s challenges on global pharmaceutical industry and analyze driving factors of competition. I briefly give the industry definition describing the scope of the analysis. The paper has the following major goals: 1) To analyze the current situation, major competition challenges and the prospects of the pharmaceutical industry; 2) To assess Pfizer’s
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Introduction Drug development from initial discovery of a promising target to the final medication, is characterized by a high degree of scientific, regulatory and economic risk. Colossal amounts of time, effort, and money are invested in the research and development process to bring a new medicine to the market. In fact, it takes an average of 10 to 15 years to bring a drug from discovery to approval, and for every 5,000-10,000 compounds investigated; only one is approved and marketed.
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