Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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Describe the issues associated with drug safety after FDA approval
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- To get approved by the FDA generic drugs have to demonstrate the following: That their bio availability is the same as brand name drug That their bio equivalence is the same as the brand name drug That their bio availability AND bio equivalence is the same as the brand name drug None of the abovearrow_forwardWhat is the meaning/definition of parent drug? And give its function and examples.arrow_forwardCritically examine Administration of Dangerous Drug Act policy in the hospital/healthcare settings and present the strengths and weaknesses.arrow_forward
- Explain what is meant by a drug’s spectrum and how narrow- andbroad-spectrum drugs differ.arrow_forwardExplain why drugs are classified legally into differentschedulesarrow_forwardBriefly discuss reasons why metabolism is a major cause of variations in drug response and or toxicity amongst patientsarrow_forward
- Explain how legal and ethical frameworks underpin safe and effective medicinesmanagement and administration.arrow_forwardCritically examine the Administration of Dangerous Drug policy and present the strengths and weaknesses.arrow_forwardOutline some important factors to consider in drug therapy.arrow_forward
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