Q. No 2. Answer :
As the age increases the functions of tissues and organs may decreases gradually, so that the absorption, metabolism, and distribution of medications and elimination of drugs may decreases in the old age people.
By using of some psychotropic drugs, the drug sensitivity observed in elderly like increased blood pressure.
Infants also more sensitive to drugs as the immature organs.
Q. No 3. Answer :
The drugs are metabolism taken place in the liver and excretion taken place by kidney, as the diseases to liver and kidneys there is no proper metabolism and absorption and excretion, so that the effect of drugs will not good.
Q. No. 4. Answer :
Pharmacodynemic tolerance : It is defined as it is an instances of tolerance it involves adoptive changes in the receptor binding and recruitment of processes that limits.
Metabolic tolerance :
It is also known as pharmacology kinetics tolerance, it refers to the obsorption, distribution, metabolism and excretion of drugs.
Tachyphylaxis :
It is acute sudden decrease responses to a drug after administration, and that is a rapid and short term onset of drug tolerance.
Q. No 5. Placebo effects : it also called as placebo response, it is a fake treatment, inactive substances like sugar, distilled water and saline solution, by using these some times may patients feel satisfaction because they feel like effect of active medicine.
Benefits of these some times patients may get satisfy, because one of the psychological feeling, with the medicine taking only they will cure like that, so that time it may helpful.
Negative effects also called as 'nocibo effect' after receiving treatment they is no effect or inactive.
Discuss the significance of body weight and composition, focusing on the effect of weight and the...
Discuss the pharmacokinetics of children 1 year old or older. Discuss reasons pediatric patients are subject to adverse drug reactions when drug levels rise too high. Discuss dosage determination, noting that pediatric doses have been established for some drugs but not for others and, therefore, for drugs that do not have established pediatric doses, the doses can be extrapolated from adult doses. Discuss the appropriate steps in determining exposure to teratogens. Discuss drug therapy during breast-feeding and the potential risks...
Provide an overview of the pharmacokinetics of neonates and infants. Discuss drug absorption in neonates and infants, focusing on a drug’s physicochemical properties and its effects on absorption. Discuss drug absorption as it relates to the route of administration in pediatric patients. Discuss factors directly related to drug distribution in neonates and infants (e.g., protein binding and the blood–brain barrier). Discuss hepatic metabolism and compare the drug-metabolizing capacity of a newborn with that of a 1-year-old infant. Discuss renal excretion...
Define pharmacodynamics and its relationship to the action of drugs on the body. Discuss dose-response relationships (e.g., basic features of the dose-response relationships, maximal efficacy, and relative potency), the effects drugs can produce, and the amount of drug needed to elicit an effect. Discuss properties of drug-receptor interactions (e.g., drug receptors, four primary receptor families, receptors and selectivity for drug action, theories of drug-receptor interaction, agonists, antagonists, partial agonists, and regulation of receptor sensitivity). Describe how receptors function in the...
Discuss the consequences of drug–drug interactions, the basic mechanisms of drug–drug interactions, and the critical steps in minimizing adverse drug–drug interactions. Focus on the liver as an example of a drug-metabolizing system and explain why it is such a crucial organ in many drug–drug interactions. Discuss the effect of food on drug absorption, on drug metabolism (e.g., grapefruit juice), and on drug toxicity and action, as well as the timing of drug administration with respect to meals. Give examples of...
Discuss the scope of the problem of adverse drug reactions. Discuss definitions for adverse drug reactions (e.g., side effect, toxicity, allergic reaction, idiosyncratic effect, iatrogenic disease, physical dependence, carcinogenic effect, and teratogenic effect). Discuss organ-specific toxicity. Focus on the liver as a drug-metabolizing system and explain why it is such a crucial participant in organ-specific toxicity with drugs. Discuss how and why adverse drug reactions occur, given that for a prescription drug to be approved for use, it must have...
Chapter 2: 1. Routes of administration p 14 2. Pharmacokinetics: ADME, p 14, body systems involved what affects ADME. 3. Half-life, p 15. 4. Ryes syndrome 5. Desired therapeutic range/therapeutic window, p 17. Chapter 3: 1. Placebo vs nocebo p 22. Age implications for drug administration, p 28. Why elderly are at higher risk for drug interactions? 2. Chapter 12 1. 2. Adrenergic agonists p 176 and blockers p. 180. Anticholinergic effects and side effects p 183. Chapter 19 1....
QUESTION 9 Long-term use of stimulants can lead to A. an increase in body weight B. stimulant psychosis C. sensitization to the euphoric effects D. all of the above QUESTION 10 the presynaptic terminal Amphetamine produces its effects mainly by _ A. blocking the reuptake: dopamine into B. decreasing the release: serotonin from Cincreasing the release: GABA from Dincreasing the release: dopamine from QUESTION 11 Nicotine produces its effects by A stimulating muscarinic acetylcholine receptors B. blocking acetylcholine receptors C....
5. Most drug metabolize in the a skin b. kidneys c. stomach d. liver e, intestines 16. What populations may have issues metabolizing medications? a. Younger children b. Older adults c. Those with kidney disease d. All of the above e. A and B 17. Most drugs are excreted through the a. skin and large intestine b. large intestine and kidneys c. large intestine and lungs d. lungs and kidneys e. kidneys and skin and 18. What are the concerns...
Chapter 57 1.Explain the glycosylated hemoglobin (hemoglobin A1c), what it reflects (in terms of blood chemistry), and why it is an important adjunct to (total) blood glucose levels in monitoring the response of diabetes to therapy. 2. Be able to discuss diabetic ketoacidiosis 3. Identify the main groups of oral antidiabetic drugs (and a prototype in each). Compare and contrast their main mechanisms of action, their main adverse responses, and drug–drug interactions 4. State three classic signs or symptoms of diabetes and identify...
Question 17 Conscious or moderate sedation is a form of general anesthesia, it results in partial or complete loss of consciousness without reducing normal respiratory drive. True or False a. True b. False Question 18 Duration of action is a. The time it takes for the drug to elicit a therapeutic response b. The time it takes a drug to reach its maximum therapeutic response C. A corresponding response to increasing drug concentrations at the site of action d. The...