Find the (A) innovator brands of these drugs, (B)leading brands in the Philippine market and the (C) taxonomical source of these drugs Donepezil Edrophonium Demecarium Physostigmine Pyridostigimine Amberonium Parathion Malathion EchoThiophosphate IsoptoFluorophosphate
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- Find the (A) innovator brands of these drugs, (B)leading brands in the Philippine market and the (C) taxonomical source of these drugs
- Donepezil
- Edrophonium
- Demecarium
- Physostigmine
- Pyridostigimine
- Amberonium
- Parathion
- Malathion
- EchoThiophosphate
- IsoptoFluorophosphate
Step by step
Solved in 3 steps
- Which of the statements below is true about pharmaceutical or drug packaging? a.) FDA maintains tight control over regulations b.) cost is a major consideration when designing a package c.) advertising and communicating with the consumer is important for both prescription and OTC drugs. d.) shelf life is always shorter than for food so must choose material appropriately.The acronym, USP, referenced on the Data Analysis page refers to the United States Pharmacopeia. Which of the following statements is not true about the USP? a) mission is to improve global health by issuing public standards and related programs to ensure the quality, safety, and benefits of medicines and foods b) generates chemical reference standards and official test methods for medicines and foods to ensure their quality and safety c) is responsible to provide the U.S. with a reliable, affordable, universal mail service d) is a non-profit scientific organization founded in 1820 in Washington D.C.23) Antipsychotics account for A) 20 B) 30 C) 40 percent of all prescriptions written in the United States. 23) D) 50
- The "gold standard" of drug efficacy studies is the double-blind, placebo-controlled design. Which of the following most likely prevents our ability to reach firm conclusions? A) We cannot conduct this type of research due to federal rules regarding research ethics. B) Participants can usually tell the difference between an active drug and a placebo. C) Observers typically know which participants are taking the placebo. D) Most of the drugs we wish to test are technically illegal.What is Drugbank? https://go.drugbank.com/ A.A compendium of drugs that are commercially available. B.Drug Gene Interaction database C.FBI storage locker for illegal drugs D. A database of pharmaceutical knowledge about drugs.NEED BOTH QUESTION WITH EXPLANATION. .. ....DON'T ATTEMPT IF YOU ARE GOING TO ATTEMT ONLY ONE QUESTION Question 31 Medicaid is mostly for A) disabled veterans B) age 65 or older C) residents of Puerto Rico D) low income Question 32 Managed care organizations do not have to accept Medicaid due to A) It is not licensed B) It is run by the city C) It has varied rates D) It is not accredited
- When a medical chart requires you to use "approved" drug names, to which of the following does it refer? A) IUPAC B) Generic C) Chemical D) TradeThis drugs in the picture can treat: A) malaria B) cough C) pain D) arrhythmiaMail order pharmacies: these are true, except: A) Can fill large volumes of prescriptions B) Only need to follow the Federal Pharmacy requirements C) used for chronic conditions D) often less expensive
- NEED ALL THREE QUESTION WITH EXPLANATION (MULTIPLE CHOICE) Question 27 Part D of Medicare covers A) 80% of outpatient services B) hospital services C) prescriptions D) 20% of outpatient service Question 28 In order to contract with a managed care organization A) providers must accept Medicaid B) providers must accept Medicare C) providers must accept TRICARE D) all of the above Question 29 Medicaid is A) a state program B) a federal program C) a city program D) a private programWhy would a multinational pharmaceutical company stymie the entry of a generic drug product into the market? Outline legal barriers to the entry of generic drug products into the market.The Food and Drug Administration (FDA) is responsible for: A. Requiring drug manufacturers to provide notice that a new drug is safe. B. Recalling pharmaceuticals only after harm has occurred. C. The approval before a new drug can be marketed. D. The assumption that the manufacturer of drugs would have conducted safety tests before marketing a new drug and protocols have been established.