NUR 641E Final Exam Questions and 100%Correct Answers 2024 (Updated).

NUR 641E Final Exam Questions and 100%Correct Answers 2024 (Updated). Pharmacokinetics involves - Correct Answer-absorption, distribution, metabolism and elimination). Absorption: - Correct Answer-absorption from the administration site either directly or indirectly into the blood/plasma. Distribution: - Correct Answer-reversibly or irreversibly move from the bloodstream into the interstitial and intracellular Metabolism: - Correct Answer-biotransformed via hepatic metabolism or by other tissues. Elimination: - Correct Answer-tissues. lastly, the drug and its metabolites are eliminated from the body. route of administration with the highest bioavailability - Correct Answer-intravenous; putting entire dose into a patient's vein and bypassing absorption. avoids first-pass metabolism - Correct Answer-Intravenous route administration has variable and erratic absorption. n - Correct Answer-Rectal administration 4. Steady state (SS) - Correct Answer-absorption. n is usually reached within 4-5 halflives of drug. Half-life of a drug is - Correct Answer-how long it takes for half the drug to be excreted from the body. Determines how frequently the drug must be administered. Predicts how long toxic effects can constant with first-order pharmacokinetics of a drug. Zero-order (nonlinear) pharmacokinetics - Correct Answer-means a drug is metabolized at a constant rate per unit time. CYP3A4 substrate drugs - Correct Answer-may have enhanced activity if any CYP3A4 inducer drugs are used along with it. Drug development process involves these steps according to the FDA: - Correct Answer-Discovery: laboratory research to develop the new drug. Preclinical research with animal testing for safety (Phase I). Clinical research on human subjects for medication safety (Phase II). Clinical research in humans comparing the new drug to NUR 641E Final Exam 2024 (Updated). accepted medications placebo depending on the study (Phase III). FDA review of the results to determine approval. Post marketing study to identify adverse effects not found in earlier clinical studies (Phase IV) 2. Medication safety organizations - Correct Answer-The Institute for Safe Medication Practices (ISMP) The Institute of Medicine (IOM) The Joint Commission The National Coordinating Council for Medication Error Reporting and Prevention (NCC MERP) Food and Drug Administration (FDA) Safe Use Initiative Two basic type of ADRS: - Correct Answer-pharmacological and idiosyncratic. 85% to 90% of ADRS - Correct Answer-are pharmacological. Adverse drug reactions are usually preventable, - Correct Answer-frequently occur in a hospital or nursing home setting, and include medication errors, adverse drug effects, and allergic idiosyncratic type reactions. ADRS are not commonly reported; - Correct Answer-the FDA does not mandate that ADRS be reported. Polypharmacy - Correct Answer-involves using multiple health care providers for care, using multiple medications, and using several pharmacies prescription filling. Angiotensin converting enzyme inhibitors (ACEIS): - Correct Answer-lisinopril, captopril, enalapril, ramipril, benazepril, fosinopril. ACEIS reduce blood pressure enzyme. - Correct Answer-by suppressing the release of angiotensin-converting enzyme. Important side effects of ACE inhibitors - Correct Answer-Important include cough and angioedema; discontinue the ACEI if angioedema occurs. Angiotensin II receptor blocking agents (ARBS): - Correct Answer-Icandesartan (Atacand), eprosartan (Teveten), irbesartan (Avapro), losartan (Cozaar), telmisartan (Micardis) and valsartan (Diovan). ARBS reduce blood pressure - Correct Answer-by blocking angiotensin II receptors. Essential (primary) hypertension - Correct Answer-Essential (primary) accounts for 90% of cases; secondary hypertension may caused by chronic renal failure. Nitroglycerin - Correct Answer-Nitroglycerin is a nitrate drug that can be administered IV, SL, a topical ointment and as a transdermal patch.