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STEM Workplace Practices Q3
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- The total dosage amount that is given to a patient in a day to achieve therapeutic effect. Minimum dose Maintenance dose Daily dose Single dosePhase II drug trials are conducted on animals, while Phase III drug trials are conducted on healthy volunteers. Both are required for FDA approval. True FalseThe FDA recommends all risk characterizations should follow TCCR Principles. Which of the following are NOT terms represented in this acronym? CHOOSE ALL THAT APPLY OA, reasonableness B. relevance OC. tactfulness OD. clarity E, candidness OF, transparency G. consistency
- 17. Human plasma-derived products characteristics. The application of human plasma-derived products in the diagnostic and treatment of diseases. Quality control.2. List down the utensils, apparatus and other equipment and materials for all level hospitals in accordance with BFAD rules and regulations. 3. Provide a list of the most important reference materials used in the hospital pharmacy.Order: furosemide (Lasix) 40 mg PO Q12H Pharmacy supply: 10mg/mL How much will you give your patient? Order: gentamicin 50 mg IM Q8H Pharmacy supply: 40 mg/mL liquid? How much will you give your patient? Round to the nearest hundredth
- Education is a critical elements of Standard Precautions but training is not required Question options: A) True B) FalsePlease explain in your own words your understanding of the NSQHS Medication Safety Standard. Please provide a detailed example from your clinical placements of this standard to your practice (the example must be presented using the STAR format).A patient is to take a course of prednisolone for 6 weeks. The starting dose is 10mg daily for two weeks then reduce by one tablet in the third week, then another reduction of one tablet in the fourth week until a maintenance dose of 2.5mg for the last 2 weeks. How many prednisolone 2.5mg tablets should be dispensed? units – tablets
- SAFE DRUG ADMINISTRATION A nurse is caring for a client in the intensive care unit with an IV nitroglycerin drip. The student nurse asks why there is special tubing with this IV. What is the correct rationale? 1. The drug is light-sensitive. 2. The hospital is switching IV products. 3. Nitroglycerin reacts with plastic tubing. 4. The IV does not need special tubing.3. An ongoing clinical protocol at your site includes weekly blood draws to assess an exploratory endpoint. Unfortunately, participants are not happy about visiting the clinic weekly, and they are considering dropping out. Therefore, a protocol amendment is being prepared to remove the weekly blood draw. This change can be implemented: O A. Immediately, as it is not a safety assessment. O B. Once the protocol is finalized and submitted to the FDA. O C. Once the protocol and consent form updates are approved by the IRB. O D. As soon as the study sponsor advises that their decision is final to remove these blood draws. If already serving as a member of the IRB, a clinical investigator can participate in the review of her own clinical protocol. O A. TRUE O B. FALSE An IRB may perform an expedited review of a protocol or informed consent form change if the change involves no more than minimal risk to study participants. O A. TRUE O B. FALSECreate a set of Risk Management Plan for an effective conduct of product recall in a community pharmacy setting and Hospital Pharmacy Setting.
