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An overview of various aspects of medical devices and pharmaceutical drugs, including diagnostic equipment, advanced medical therapies, drug approval processes, clinical trials, pharmacology concepts, drug administration, drug interactions, and drug development. It covers topics such as the average review time for new drugs, the role of placebos in clinical trials, the study of drug effects and mechanisms, routes of drug administration, drug recalls, and the costs associated with drug r&d. The document touches on key concepts in the fields of medical devices, pharmaceuticals, and clinical pharmacology, making it potentially useful for students, researchers, or professionals interested in these areas.
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Pharmaceuticals - Medicines/ vaccines /human and animal use. / trademark (brand) name or generic/and prescription or over-the counter. Diagnostic - All Equipment /supplies- screening/detecting, and monitoring disease./ Medical Devices - Advanced instrument /medical therapy, / joint replacements, defibrillators, and pacemakers./includes drug delivery devices such as syringes, infusion pumps, metered-dose inhalers, and transdermal patches. Medical Supplies - Commodity, supplies such /surgical gowns and gloves. Durable Medical Equipment - Reusable products/ walkers, wheelchairs, oxygen equipment, prosthetics and hospital beds. What countries are pharmaceutical sales the highest? - United States, Western Europe, and Japan. The U.S. accounts for roughly___of the world's pharmaceutical revenues. - 50% Two factors have significantly contributed to recent growth in the pharmaceutical industry are? - Population growth/ increasing life expectancies. What is the predicted relationship between pharmaceutical companies and genomic research facilities? - Partnership will not prove immediately profitable.
Prescription drug therapy is cost effective for insurance companies and health care providers. True or False?
on each physician's specific needs.
Pharmaceutical reps mainly visit pharmacies. True or False? - False. Pharmaceutical reps mainly visit/target physicians. It usually takes only 1-2 calls on a physician before he or she prescribes your product. True or False? - False. Your success ultimately depends on your relationship with the physician. This takes time. Persistence is key. The pharmacist may dispense a product other than what the physician prescribed. True or False? - True. The pharmacist can either (1) dispense a generic; (2) The pharmacist calls the doctor and requests permission to dispense a different medication. According to chapter 2 of your manual which of the following classifies as payers? (a)employers (b)patients (c)pharmacists (d)physicians - (a) employers Some third party payers include the insurance company, the employer, managed care organization, or the U.S. government (Medicare/Medicaid). What defines ethical pharmaceutical companies? - Pharmaceutical companies that research and develop novel drugs. Thanks to modern medicine how long are people newly diagnosed with HIV expected to live? - Another 50 years.
How much has the average American lifespan increased since 1890? - 30 years
What is a treatment group? - A group of patients assigned to receive specific treatment. What is the main difference between a blinded and double-blinded study? - In a double blinded study, neither the staff nor the study participants know which subjects are in the experimental group and which subjects are in the control group. What does asymptomatic mean? - Without signs or symptoms of disease. What is an approvable letter? - Letters sent by the FDA to the applicant indicating whether the new drug application (NDA) or abbreviated new drug application (ANDA) for a product meets the necessary requirements and whether or not the agency believes that it can approve the application or abbreviated application if specific additional information or material is submitted or specific conditions (e.g., certain changes in labeling) are agreed to by the applicant. What is a blinded or masked study? - A study in which participants do not know whether they are in the experimental or control group of a research study. Those in the experimental group get the medications or treatments being tested, while those in the control group get standard treatment or no treatment. What is a control or control group? - The standard by which experimental observations are evaluated. In many clinical trials, one group of patients will be given an experimental drug or treatment, while the control group is given either a standard treatment for the illness or a placebo. What is a double-blind or double-masked study? - A study in which neither the participants nor the study staff know which participants are receiving the experimental treatment and which patients are in the control group. These studies are performed so neither the patient nor doctor expectations about the experimental drug can influence the outcome.
What is edema? - Swelling. What are fast-track drugs? - Fast-track drug approval is provided for drugs that meet medical needs for patients with serious or life-threatening conditions.
What is indication in terms of drug approval? - The exact cause or purpose for which the FDA has approved that a new drug can be prescribed. What is the institutional review board (IRB)? - A committee of physicians, statisticians, community advocates, and others which ensures that a clinical trial is ethical and that the rights of the study participants are protected. All clinical trials in the U.S. must be approved by the IRB before they begin. What does the term "off label" mean? - Usage of a medication for purposes other than the specific ones appearing in the labeling. What is a placebo? - A placebo is an inactive pill, liquid, or powder that has no treatment value. In clinical trials, experimental treatments are often compared with placebos to assess the treatment's effectiveness. What is the placebo effect? - The effect produced by a placebo due to the expectations of the patient. The effect in placebo-controlled clinical trials is generally measured by comparing the effect observed in patients receiving the placebo treatment to the effect observed in patients receiving the active treatment. What is study protocol? - The general design and operating features of a trial. It is distinguished from the study manual operations by its generality and absence of specific details needed for day-to-day execution of the trial. Define toxicity. - The extent, quality, or degree to which a substance is poisonous or harmful to the body. Define "anatomy" - The study of the basic structures of the body.
Define "physiology" - The study of how those body structures function Define "clinical pharmacology" - The study of the effects and movements of drugs in the human body.
Define "pharmacodynamics" - Study of biochemical and physiological effects of drugs and their mechanisms of action, i.e., the study of what a drug does to the body. Drug dynamics (pharmacodynamics) describes the therapeutic effects of drugs (e.g., pain relief, blood pressure reduction), their side effects, their sites of action (i.e., which tissues they act on), and their mechanisms of action (i.e., how they act on those tissues). A drug's effects on the body may be influenced by many factors, such as a person's age and genetic makeup and disorders the person has other than the one being treated. Define "pharmacokinetics" - Study of how a drug is processed by the body, with emphasis on the time required for absorption, duration of action, distribution, and method of excretion, i.e., the study of how the body affects drugs. Drug distribution and elimination - Drug delivery systems, route of administration, modes of excretion (passing from the body). About __ people in the U.S are slow acetylators? (a)1% (b)5% (c) 25% (d) 50% - 50% of people are slow acetylators. Where is this in the book? Which statements are/is INCORRECT about an ideal drug or magic bullet as Ehrlich phrased it? (a)it does not exist (b)it would be aimed precisely at the disease site (c)it would not harm healthy tissues
(d)All of these statements are correct - (d) All of these statements are correct Which term denotes the study of bodily functions? - Physiology
What is the broadest definition of a drug? - Any substance that produces a physical or psychological change in the body. How does the Federal Food, Drug and Cosmetic Act (FFDCA) define a drug? - Any substance intended for use in the diagnosis, cure, mitigation, treatment or prevention of a disease or a substance other than food intended to affect structure of function of the body. What is true about vitamins? - Most of the body's required vitamins must be taken in from outside the body. What does ADME testing measure? - The rate at which the body absorbs the drug, distributes it to the organs necessary to produce the desired effect, metabolizes it into waste material and then excretes it from the body. ADME testing is primarily used in what field? - Pharmacokinetics What is true about placebos? - Effects can lead to withdrawal symptoms. On average, what percent of drugs are studied in the lab are eventually studied in people? - 5 of 4000 What is true about drugs taken sublingually? - Are absorbed directly and almost immediately into the bloodstream. What are 3 of the 7 rights of the drug administration? - The right patient, the right drug, and the right dose. Pro-drugs are administered in the active for, which is metabolized into an active form. - False
The kidney of an 85 year old person excretes drugs only_as efficiently as that of a 35 year old person. - Around 50%
The normal age related disease in kidney function can help doctors determine an appropriate dosage based solely on a person age. - True What differentiates a caplet from a tablet? - Caplets are shaped like capsules and have film coatings to aid in swallowing. Where will you find the legend "federal law prohibits dispensing without a prescription"? - On the label of all prescription drugs. What happens in slow acetylators? - Drugs that are metabolized by N-acetyl transferase tend to reach higher blood levels and remain in the body longer. About______of the people in the Unites States are slow acetylators. - 50% Smoking decreases the effectiveness of some drugs. - True What about drug-drug interaction is not correct? - Drug interaction are always harmful. What about dietary supplements is incorrect? - Because dietary supplements are not drugs, interacting with drugs is not a concern. Between what percent of hospital admissions in the Unites States are estimated to be for treatment of adverse drug reactions? - Between 3% and 7% Why is noncompliance a serious public health concern? - Increasing medical care cost. Legally bioequivalence of different versions od a drug can vary by up to what? - 20%
What is no true about biologies? - They do not cause an immune response. What are the drugs that attract or bind to cell receptors in order to mimic or enhance activities by endogenous channel messages? - Agonists Which term denotes how an API works in the body? - Mechanism for action. What cements the active and inert components together to maintain cohesive portions? - Binders What does the medical abbreviation BID denote? - Twice a day. What is the medical abbreviation for as needed? - PRN Which components might cause patients different reactions to brand name and generic drugs? - Differences in inactive ingredients. Do all cells have a nucleus? - No What is the typical relationship between a drugs site of administration and site of action? - They are usually somewhat removed from each other. What is CMAX? - The peak plasma concentration on a measuring curve. What is not a main concept in pharmacology? - Pharmacoprocesses What is not a route of drug administration? - Transfugal
How are intradermal drugs delivered? - By injecting under the skin. What is an example of intravenous drug delivery? - An injection of anesthetic directly into the bloodstream. What are the major organs of the gastrointestinal system? - The mouth, esophagus, stomach, liver, pancreas, gallbladder, small and large intestines. What differentiates exclusivity from a patent? - Exclusivity is only granted upon the drugs FDA approval. What is required of an invention for it to be worthy of patent protection? - It must be novel, useful, and not obvious. A generic drug is______to the originator brand name drug in dosage, strength, safety, and quality. - Bioequivalent What is not required by the FDA's criteria for equivalency? - The drugs contain identical amounts of the same inactive ingredients. What list is generally considered the most reliable source of information on the therapeutically equivalent drug products? - Approved Drug products with therapeutic equivalence Exclusivity gives exclusive_____, is granted by the FDA and can run concurrently with a patent or not.
What is an orange book rating? - B
What is the term for chemical equivalents which when administered in the same amounts will provide the same biological or physiological availability as measured by blood and urine levels? - Biological equivalents What term denotes the dispensing of an unbranded generic product for the product prescribed? - Generic substitution What term denotes a drug that is identical or bioequivalent to the originator brand name drug in dosage form, safety, strength, route, quality, performance, characteristics, and intended use? - Generic What is the duration of a patent challenge? - 180 days How is a drug sample closet or cabinet like a grocery store shelf? - The more visibility you can give your drug the more likely that it will be prescribed. Do pharmaceutical representatives typically store and secure their own drug samples? - Yes What is sometimes the most important factor in a pharmaceutical representatives success? - Sampling What approves storage conditions for drug products? - FDA Pharmaceutical representatives must always record the amount of drug samples left and obtain a signature for the amount. - True What is prohibited by section 503 of the Federal food drug and cosmetic act as amended by the prescription drug marketing act? - The sale, purchase, or trade or offer to sell,
purchase, or trade prescription drug samples. Which entity issues monographs that define how drugs should be stored and what variance is allowed in their states contents? - United States Pharmaceutical Convention
Who regulates the drug sampling for a pharmaceutical representative? - The federal government Stores conditions for drug products or based on information supplied by who? - The manufacturer In which cases can degraded drugs sometimes still be used? - When the amount of remaining drug has not fallen lower than 85-90% of that stated on the label. Drug recalls are almost always negotiated with the FDA before hand. - True What should you do if you receive a shipment from your employer and you noticed that there are twice as many samples as what is posted on the packing slip? - Call your sales manager to inform them of the mistake and ask for instructions on proper procedure. Which of the following drug R & D has seen the largest cost increases? - Clinical trials On average, how long does it take for a new drug to be developed (from the discovery of the initial compound to FDA approval)? - 10-15 years Which of the following regulatory agencies is industry based (run mainly by the companies themselves)? - Pharmaceutical Research and Manufacturers of America The landmark FDA modernization act of 1997 was a major step forward and enabling safe and effective new drugs and Biologics to be made available sooner to patients. - True
According to your manual which type of system is the best way to deliver healthcare? - A market bases system
How would increased pharmaceutical price controls affect the US healthcare system? - Increased price controls would stifle innovation. What was the intent of the Bayh-Dole act and the Stevenson-Wydler technology innovation act? - To hasten the commercialization of technologies that otherwise might not be used. According to your manual what did the G 10 medicines group recently report about the pharmaceutical industry in the European Union? - There is poor collaboration between publicly and privately funded research centers. What is the aim of preclinical pharmacological studies? - To obtain data on the safety and effectiveness of the lead compound. Toxicity information in preclinical studies helps provide what? - Confidence about a drugs safety. Pharmacological studies using animals are regulated under what? - Good laboratory practice Why do drugs administered to patients only contain API's? - They don't Which of the following does not affect a drugs ability to permeate membranes? - The drugs vesicles Through which barriers can lipid soluble drugs usually pass? - Cell membranes How are weak acid drugs generally absorbed by the stomach? - More quickly than weak basic drugs.
Which of the following routes of administration do not completely bypass the liver? - Rectal administration
Why are intravenous drug dosages easier to control than drugs administered transdermally? - The entire dose is available in the bloodstream to be distributed to the target site. What medical term means to apply the drug on the skin surface? - Transdermal Carcinogenicity studies are meant to identify the tumor causing potential of a drug. - True According to NIH ethical guidelines, which of the followers is the most important criteria in selecting subjects for clinical studies? - Scientific objects Which statement about the IRB is incorrect? - The members of the IRB/IEC must be experts in the topic of study. Which phases of clinical studies are open label and which are blinded? - Phase 1 and 4 trials are often open label, but phase 2 and 3 are double blinded or at least blinded. If it is not possible to measure the direct effects of a drug, what is used instead? - Surrogate markers such as blood pressure and cholesterol levels. Which of the following is an observational study that first identifies a group of subjects with a certain disease and a control group without that disease, and then looks to back in time (via chart reviews) to find exposure to risk factors? - Case control study Which measure of central tendency is the sum of all observations divided by the number of observations? - Mean
Which measurement describes the number of new events that occur during a specified period of time in a population at risk for the event (lung infections per year)? - Incidence