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1. Why would it be important to have CLIA kits listed here?
2. Can a POL use kits that are not listed on the "current waived analytes" on the FDA website?
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- 1) COVID-19 a. Should there be clinical trails performed by agents (institutions) outside the very drug companies that manufacture them? b. Which factors influence the form of treatment in any given nation (example, amount of moeny, profits to be made, accessibility of the treatment, etc.) c. Which type od approaches you think may work the best in form of minimizing COVID-19 infections and the resulting side effects4. CHOOSE THE RIGHT ANSWERS: according to Federal Law of the Russian Federation "On Circulation of Medicines" No. 61-FZ (chapter 12, article 60) state regulation of prices for medicinal products for medical use is carried out by means of: a) approval by the Government of the Russian Federation of a list of vital and essential medicinal products; b) approval of the methodology for determining the manufacturers' maximum ex-works prices for the medicinal products included in the list of vital and the essential medicinal products and introduction of mechanisms for creating a system of reference prices; c) state registration of the manufacturers' maximum ex-works prices for the medicinal products included in the list of vital and essential medicinal products; d) maintaining of the state register of the manufacturers' maximum ex-works prices for the medicinal products included into the list of vital and essential medicinal products; e) approval of the methodology for determination by…1.- Please name the drug sources, and explain one of them. 2.- Why are important the Drug Standards? 3.- What means: PDR and USAN? 4.- Please explain the Controlled Substances Act of 1990. 5.- What is the Food Allergen Labeling and Consumer Protection Act of 2004? Why is important? Please give an example of one product label. 6.- What is Pharmacokinetics? What means excretion of a drug? 7.- Which factors can change the drug absorption? 8.- Please name the factors that can affect the Drug Action, and explain one of them. 9.- What is an adverse reaction? 10.- What is a palliative drug?
- 1. Create drug study of PROPRANOLOL that includes the GENERIC NAME, CLASSIFICATION, PHARMACODYNAMICS, INDICATIONS AND 10 NURSING CONSIDERATIONS. 2. Create drug study of PARACETAMOL that includes the GENERIC NAME, CLASSIFICATION, PHARMACODYNAMICS, INDICATIONS AND 10 NURSING CONSIDERATIONS. Thank you! :)5. A physician orders Vistaril 50 mg IM stat for a patient with pruritus (itching). The patient weighs 132 pounds. A. What is the recommended dosage range in mg for this patient? B. Is the dose safe as ordered? C. How many mL of Vistaril should be injected? D. What is the maximum recommended mg per day?Types of specimens are given. Match the following to their advantage. A. Less contaminated by bacteria B. No interference C. Assurance of unadulterated specimen based on its temperature D. Better understanding on glucose metabolism E. Does not contain CHO metabolites F. Concentrated G. Collected as needed H. Sterile specimen from a child 1. Midstream Clean Catch 2. Random 3. Drug specimen collection 4. 8-hour specimen 5. Glucose tolerance 6. Pediatric 7.Fasting
- According to USP Chapter which of the following scenarios would indicate that the specialty product prepared has a high risk level of contamination? Select one: O a. A specialty product prepared with a unique formulation of 2 sterile ingredients O b. P A specialty product prepared not administered via the intravenous route O c. A specialty product prepared with nonsterile components O d. A specialty product prepared with 2 sterile ingredients attempt.php?attempt=190453&cmid=102374&page=22# Q Search 10 F 14 Know a5. Potassium chloride liquid is available in 20 mEq/15mL concentration. The patient needs 50 mEq two- times a day. a.) How much will be used for one dose? b.) How much will be used daily?1. If excipients do not have pharmacodynamic activity, how do excipients affect the performance of the drug product? 2. What is meant by the rate-limiting step in drug bioavailability from a solid oral drug product? 3. What is the usual rate-limiting step for a poorly soluble and highly permeable drug (BCS 2)? 4. How could the manufacturing process affect drug product performance? 5. Drug absorption involves at least three distinct steps: dissolution, permeation, and disposition during transit in GI (an additional step of drug disposition in the body is involved as well for bioavailability). How are these processes validated in vitro when the in vivo requirement for drug bioavailability is waived? 6. What is meant by “sink” conditions? 7. What physical or chemical properties of a drug substance are important in designing a drug for (a) oral administration or (b) parenteral administration? 8. For a lipid-soluble drug that has very poor aqueous solubility, what strategies could be…
- Explain three functionally distinct compartments in drug absorption 1.intracellular compartment 2.plasma compartment 3.interstitial compartment1. What happens if sample for Potassium determination is refrigerated? What causes the variation? 2. What is the role/importance of Potassium in the body metabolism? 3. In doing the assay, why is hemolyzed sample not allowed?Please give these information for this drug named Atogepant. 1) Indications 2) Usage 3) Dosages and Administration 4) Contraindication 5) Use in specific population 6) Dosage form and Strength. Please shortly answer at your own easy words. Answer should be to the point.