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TOP 2025/2026 NSG 552 Psychopharmacology Exam with Q&A 100% ACCURATE

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TOP 2025/2026 NSG 552 Psychopharmacology Exam with Q&A 100% ACCURATE What are the 6 general principles of psychopharmacological treatment? Safety Tolerability Efficacy Practicality Treatment accessibility Treatment compliance Pharmacokinetics How the drug moves in the body. (ex. Where is it absorbed? How and where is it metabolized? Where is it excreted?) Pharmacodynamics What the drug does to the body. (consider the mechanism of action) Define First-generation antipsychotics Referred to as Typical Antipsychotics. Most have strong bonds with D2 receptors only, cause EPS symptoms faster due to prolonged receptor dissociation, have more dangerous side effect profiles, have been around longer, more effective at treating positive symptoms, less expensive. (Ex. Haloperidol, Chlorpromazine, Thioridazine, Fluphenazine) Define Second-generation antipsychotics Referred to as Atypical Antipsychotics. Most have a weak bond with D2 receptors and block serotonin receptors leading to anti-depressive and anxiolytic effects. They cause less EPS due to rapid receptor disassociation which leads to rapid dopamine neurotransmission. Have less dangerous side effect profiles but can cause metabolic syndromes, have been around shorter time, more expensive, more effective at treating negative symptoms but can treat positive symptoms as well, long-acting injections are available for several of these. (Ex. Risperidone, Clozapine, Quetiapine, Aripiprazole, Ziprasidone) Extra Pyramidal Symptoms (EPS) Side effects caused by certain antipsychotic medications, which include: involuntary or uncontrollable movements . tremors . muscle contractions . Tardive dyskinesia A neurological disorder characterizes by involuntary movement of the face and jaw. Upregulation Occurs through chronic use of antagonists which causes an increase in the number of receptors, externalization of receptors, and increased sensitivity of the receptors. Prolonged use of antagonist - Up-regulation of receptors - Sudden withdrawal of antagonist - increased number of receptors and increased sensitivity of receptors *Y OU MUST GRADUALLY TAPER A DRUG TO AVOID BINDING TO ALL NEW RECEPTORS FROM UPREGULATION Down-regulation Occurs by chronic exposure of agonists which causes decreased number of receptors, internalization of receptors, and decreased sensitivity of the receptors. Prolonged use of agonist - down-regulation of receptors - decreased effectiveness of agonist-mediated clinical response . You have two options: 1 Increase the drug dose OR 2 Switch to another drug(BEST OPTION) Receptor profile The receptors that each drug binds to (For example, risperidone's receptor profile would like... (a) Blockade of 5HT2A and D2 receptors (b) High affinity for a1, a2, and H1 receptors) Binding Refers to a drug metabolite or neurotransmitter attaching to a receptor Affinity refers to the "preference" or likelihood of a drug to bind to a certain receptor. Linked to potency. CYP450 A group of enzymes in the liver that metabolize different drugs. There are six. List the 7 CYP450 Enzymes (1) CYP1A2 (2) CYP2B6 (3) CYP2C9 (4) CYP2C19 (5) CYP2D6 (6) CYP3A4 (7) CYP2EI CYP2B6 Metabolizes artemisinin, bupropion, cyclophosphamide, efavirenz, ketamine, and methadone (2B6, there are two psych drugs (bupropion, methadone (ketamine...?) and six altogether. CYP1A2 metabolizes AcetAminophen (two As) CYP2C9 metabolizes Warfarin/Coumadin (think warfarin factors 2, C, 9) CYP2C19 metabolizes PPIs, antidepressants, antiplatelet, antifungals, and anticancer drugs (2C19, two see one, there is only one class of psych drugs that are metabolized, you ONLY SEE one! antidepressants) CYP2D6 Metabolizes Cardiovascular drugs (2-D echo, echo is a test for heart) CYP3A4 Most common and ambiguous (if not above, then it's this one, a lot of psych drugs are involved with this one) CYP2EI ETOH (You have to be 21 to drink) CYP450 inhibitors Decreases drug metabolism: (1) Valproate (2) Ketoconazole (3) Isoniazid (4) Sulfonamides (5) Chloramphenicol (6) Amiodarone (7) All macrolides (think mycins) except azithromycin

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NSG 552
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Voorbeeld van de inhoud

‭ OP 2025/2026 NSG 552‬
T
‭Psychopharmacology Exam with Q&A‬
‭100% ACCURATE‬

‭ hat are the 6 general principles of psychopharmacological treatment?‬
W
‭Safety‬
‭Tolerability‬
‭Efficacy‬
‭Practicality‬
‭Treatment accessibility‬
‭Treatment compliance‬
‭Pharmacokinetics‬
‭How the drug moves in the body. (ex. Where is it absorbed? How and where is it‬
‭metabolized? Where is it excreted?)‬
‭Pharmacodynamics‬
‭What the drug does to the body. (consider the mechanism of action)‬
‭Define First-generation antipsychotics‬
‭Referred to as Typical Antipsychotics. Most have strong bonds with D2 receptors only,‬
‭cause EPS symptoms faster due to prolonged receptor dissociation, have more‬
‭dangerous side effect profiles, have been around longer, more effective at treating‬
‭positive symptoms, less expensive. (Ex. Haloperidol, Chlorpromazine, Thioridazine,‬
‭Fluphenazine)‬
‭Define Second-generation antipsychotics‬
‭Referred to as Atypical Antipsychotics. Most have a weak bond with D2 receptors and‬
‭block serotonin receptors leading to anti-depressive and anxiolytic effects. They cause‬
‭less EPS due to rapid receptor disassociation which leads to rapid dopamine‬
‭neurotransmission. Have less dangerous side effect profiles but can cause metabolic‬
‭syndromes, have been around shorter time, more expensive, more effective at treating‬
‭negative symptoms but can treat positive symptoms as well, long-acting injections are‬
‭available for several of these. (Ex. Risperidone, Clozapine, Quetiapine, Aripiprazole,‬
‭Ziprasidone)‬
‭Extra Pyramidal Symptoms (EPS)‬
‭Side effects caused by certain antipsychotic medications, which include:‬‭involuntary or‬
‭uncontrollable movements‬‭.‬‭tremors‬‭.‬‭muscle contractions‬‭.‬
‭Tardive dyskinesia‬
‭A neurological disorder characterizes by involuntary movement of the face and jaw.‬

, ‭ pregulation‬
U
‭Occurs through chronic use of antagonists which causes an increase in the number of‬
‭receptors, externalization of receptors, and increased sensitivity of the receptors.‬
‭Prolonged use of antagonist -> Up-regulation of receptors -> Sudden withdrawal‬
‭of antagonist -> increased number of receptors and increased sensitivity of‬
‭receptors *Y‬‭OU MUST GRADUALLY TAPER A DRUG TO AVOID BINDING TO ALL‬
‭NEW RECEPTORS FROM UPREGULATION‬
‭Down-regulation‬
‭Occurs by chronic exposure of agonists which causes decreased number of receptors,‬
‭internalization of receptors, and decreased sensitivity of the receptors.‬‭Prolonged use‬
‭of agonist -> down-regulation of receptors -> decreased effectiveness of‬
‭agonist-mediated clinical response‬‭.‬
‭You have two options:‬
‭1 Increase the drug dose OR‬‭2‬‭Switch to another drug(BEST‬‭OPTION)‬
‭Receptor profile‬
‭The receptors that each drug binds to‬
‭(For example, risperidone's receptor profile would like...‬
‭(a) Blockade of 5HT2A and D2 receptors‬
‭(b) High affinity for a1, a2, and H1 receptors)‬
‭Binding‬
‭Refers to a drug metabolite or neurotransmitter attaching to a receptor‬
‭Affinity‬
‭refers to the "preference" or likelihood of a drug to bind to a certain receptor. Linked to‬
‭potency.‬
‭CYP450‬
‭A group of enzymes in the liver that metabolize different drugs. There are six.‬
‭List the 7 CYP450 Enzymes‬
‭(1) CYP1A2‬
‭(2) CYP2B6‬
‭(3) CYP2C9‬
‭(4) CYP2C19‬
‭(5) CYP2D6‬
‭(6) CYP3A4‬
‭(7) CYP2EI‬
‭CYP2B6‬
‭Metabolizes artemisinin, bupropion, cyclophosphamide, efavirenz, ketamine, and‬
‭methadone (2B6, there are two psych drugs (bupropion, methadone (ketamine...?) and‬
‭six altogether.‬
‭CYP1A2‬
‭metabolizes AcetAminophen (two As)‬

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