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WGU D345 Objective Assessment (Latest 2026 Update) Psychopharmacology for Advanced Psychiatric Mental Health Practice Review| 100% Verified Questions & Answers | Grade A

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WGU D345 Objective Assessment (Latest 2026 Update) Psychopharmacology for Advanced Psychiatric Mental Health Practice Review| 100% Verified Questions & Answers | Grade A QUESTION what is a specific side effect of pimozide? Answer: associated with QTc prolongation and ventricular tachy QUESTION in what pathway do typical antipsychotics work to treat the positive symptoms of schizo? Answer: Decrease dopaminergic action in *mesolimbic* pathway: nucleus accumbens, fornix, amygdala and hippocampus QUESTION Which dopaminergic pathway is responsible for negative symptoms of schizo? Answer: decreased dopaminergic action in *mesocortical* pathway second generation antipsychotics help fight these better than 1st gene QUESTION Which dopaminergic pathway is responsible for EPS as a symptom of first generation antipsychotics? Answer: Block dopamine in nigrostriatal pathway QUESTION Which dopaminergic pathway is responsible for gynecomastia/ prolactinemia as a symptom of second generation antipsychotics? Answer: Block dopamine in tubuloinfundibular pathway QUESTION What are the EPS side effects and when does each of them typically occur? Answer: 1. Acute dystonia- sustained painful contraction of muscles of neck (torticollis), tongue, eyes (oculogyric crisis)- life threatening if diaphragm or airway (seen within mins/hours to days) - treatment = anticholinergics (diphenhydramine, benztropine) 2. Akathisia- anxiety, restlessness, fidgetiness, can't sit still(seen within days) - treatment = beta-blocker (propranolol) or benzos (lorazepam) 3. Parkinsonism- bradykinesia, masklike face, cogwheel rigidity, pill-rolling tremor (seen within weeks) - treatment = benztropine or amantadine (dopamine agonist/ NMDA antagonist) 4. Tardive dyskinesia- 6 months after use; writing (choreoathetoid) movements of mouth and tonge; older age is risk factor; 50% will remit most are permanent - discontinue medication, try clozapine QUESTION in general, what are the categories of side effects you see from antipsychotic drugs? Answer: 1. Antidopaminergic side effects - EPS [parkinsonism, akathasia, dystonia, tardive) - hyperprolactinemia [blocking tuberoinfundibular area; dec libido, galactorrhea, gynecomastia, impotence, amenorrhea] 2. Anti- HAM effects - antihistamine- sedation, weight gain - anti alpha1 adrenergic- orthostatic hypotension, cardiac abnormalities, sex dysfunction - antimuscarinics- hot as a harre, dry as a bone, mad as a hatter, full as a tea cup, blind as a bat (dry mouth, tachycardia, urinary retention, blurry vision, constipation, preciptaiton of narrow angle glaucoma) 3. Neuroleptic malignant syndrome (more in males early in tx w/ high potency typical antipsychotics) 4. Opthalmologic problems (retinal pigmentation w/ thioridazine, deposits in lens/ocrena with chlorpromazine) 5. Dermatologic (phosensitivty/rashes and blue-gray skin discoloraiton w/chlorpromazine) 6. Seizures- all lower threshold but low potency antipsychotics are more likely 7. elevated LFTs, jaundice QUESTION how do you treat EPS sxs? Answer: - reduce dose of antipsychotic - administer anticholinergic med such as benztropine (Cogentin) or diphenhydramine (Benadryl) or less commonly antiparkinsonian med such as amantadine (symmetrel) QUESTION what is the mortality rate of NMS if left untreated? what type of med causes it hte most? Answer: 20% mortality more with high potency typical antipsychotics QUESTION what are the characteristics of NMS? Answer: Fever Autonomic instability (tachy, labile HTN, diaphoresis) Leukocytosis Tremor Eelevated CPK Rigidity (lead pipe) Excessive sweating (diaphoresis) Delirium (mental status changes) QUESTION what is treatment of NMS? Answer: discontinue current med *dantrolene, bromocrpitine and amantadine* may be used but unclear efficacy supportive management (large bore IV, cooling pads, benzos ready for seizure activity) not prevented from starting same neuroleptic at later time but increased risk of another episode QUESTION what is the rate at which you develop tardive dyskinesia when you are treated w/ typical antipsychotic? Answer: 5% chance each year treated with typical antipsychotic QUESTION how can you monitor for tradive dyskinesia (what scale?) Answer: Abnormal involuntary movement scale (AIMS) QUESTION why do docs like to use atypical antipsychotics more than typical? (i.e. what are the benefits?)

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WGUl D345l Objectivel Assessmentl (Latestl
2026l Update)l Psychopharmacologyl forl
Advancedl Psychiatricl Mentall Healthl
Practicel Review|l 100%l Verifiedl Questionsl
&l Answersl |l Gradel A

Q:l whatl isl al specificl sidel effectl ofl pimozide?
Answer:
associatedl withl QTcl prolongationl andl ventricularl tachy



Q:l inl whatl pathwayl dol typicall antipsychoticsl workl tol treatl thel positivel symptomsl ofl
schizo?

Answer:
Decreasel dopaminergicl actionl inl *mesolimbic*l pathway:

nucleusl accumbens,l fornix,l amygdalal andl hippocampus



Q:l Whichl dopaminergicl pathwayl isl responsiblel forl negativel symptomsl ofl schizo?
Answer:
decreasedl dopaminergicl actionl inl *mesocortical*l pathway

secondl generationl
l antipsychoticsl helpl fightl thesel betterl thanl 1stl gene



Q:l Whichl dopaminergicl pathwayl isl responsiblel forl EPSl asl al symptoml ofl firstl
generationl antipsychotics?

,Answer:
Blockl dopaminel inl nigrostriatall pathway



Q:l Whichl dopaminergicl pathwayl isl responsiblel forl gynecomastia/l prolactinemial asl al
symptoml ofl secondl generationl antipsychotics?

Answer:
Blockl dopaminel inl tubuloinfundibularl pathway



Q:l Whatl arel thel EPSl sidel effectsl andl whenl doesl eachl ofl theml typicallyl occur?
Answer:
1.l Acutel dystonia-l sustainedl painfull contractionl ofl musclesl ofl neckl (torticollis),l tongue,l
eyesl (oculogyricl crisis)-l lifel threateningl ifl diaphragml orl airwayl (seenl withinl mins/hoursl
tol days)
-l treatmentl =l anticholinergicsl (diphenhydramine,l benztropine)
2.l Akathisia-l anxiety,l restlessness,l fidgetiness,l can'tl sitl still(seenl withinl days)
-l treatmentl =l beta-blockerl (propranolol)l orl benzosl (lorazepam)
3.l Parkinsonism-l bradykinesia,l masklikel face,l cogwheell rigidity,l pill-rollingl tremorl (seenl
withinl weeks)
-l treatmentl =l benztropinel orl amantadinel (dopaminel agonist/l NMDAl antagonist)
4.l Tardivel dyskinesia-l >6l monthsl afterl use;l writingl (choreoathetoid)l movementsl ofl
mouthl andl tonge;l olderl agel isl riskl factor;l 50%l willl remitl mostl arel permanent
-l discontinuel medication,l tryl clozapine



Q:l inl general,l whatl arel thel categoriesl ofl sidel effectsl youl seel froml antipsychoticl
drugs?

Answer:
1.l Antidopaminergicl sidel effects
-l EPSl [parkinsonism,l akathasia,l dystonia,l tardive)
-l hyperprolactinemial [blockingl tuberoinfundibularl area;l decl libido,l galactorrhea,l
gynecomastia,l impotence,l amenorrhea]
2.l Anti-l HAMl effects
-l antihistamine-l sedation,l weightl gain

,-l antil alpha1l adrenergic-l orthostaticl hypotension,l cardiacl abnormalities,l sexl dysfunction
-l antimuscarinics-l hotl asl al harre,l dryl asl al bone,l madl asl al hatter,l fulll asl al teal cup,l
blindl asl al batl (dryl mouth,l tachycardia,l urinaryl retention,l blurryl vision,l constipation,l
preciptaitonl ofl narrowl anglel glaucoma)
3.l Neurolepticl malignantl syndromel (morel inl malesl earlyl inl txl w/l highl potencyl typicall
antipsychotics)
4.l Opthalmologicl problemsl (retinall pigmentationl w/l thioridazine,l depositsl inl lens/ocrenal
withl chlorpromazine)
5.l Dermatologicl (phosensitivty/rashesl andl blue-grayl skinl discoloraitonl w/chlorpromazine)
6.l Seizures-l alll lowerl thresholdl butl lowl potencyl antipsychoticsl arel morel likely
7.l elevatedl LFTs,l jaundice



Q:l howl dol youl treatl EPSl sxs?
Answer:
-l reducel dosel ofl antipsychotic
-l administerl anticholinergicl medl suchl asl benztropinel (Cogentin)l orl diphenhydraminel
(Benadryl)l orl lessl commonlyl antiparkinsonianl medl suchl asl amantadinel (symmetrel)



Q:l whatl isl thel mortalityl ratel ofl NMSl ifl leftl untreated?l whatl typel ofl medl causesl itl
htel most?

Answer:
20%l mortality
morel withl highl potencyl typicall antipsychotics



Q:l whatl arel thel characteristicsl ofl NMS?
Answer:
Fever
Autonomicl instabilityl (tachy,l labilel HTN,l diaphoresis)
Leukocytosis
Tremor
Eelevatedl CPK
Rigidityl (leadl pipe)
Excessivel sweatingl (diaphoresis)

, Deliriuml (mentall statusl changes)



Q:l whatl isl treatmentl ofl NMS?
Answer:
discontinuel currentl medl
*dantrolene,l bromocrpitinel andl amantadine*l mayl bel usedl butl unclearl efficacy
supportivel managementl (largel borel IV,l coolingl pads,l benzosl readyl forl seizurel activity)
notl preventedl froml startingl samel neurolepticl atl laterl timel butl increasedl riskl ofl anotherl
episode



Q:l whatl isl thel ratel atl whichl youl developl tardivel dyskinesial whenl youl arel treatedl w/l
typicall antipsychotic?

Answer:
5%l chancel eachl yearl treatedl withl typicall antipsychotic



Q:l howl canl youl monitorl forl tradivel dyskinesial (whatl scale?)
Answer:
Abnormall involuntaryl movementl scalel (AIMS)



Q:l whyl dol docsl likel tol usel atypicall antipsychoticsl morel thanl typical?l (i.e.l whatl arel
thel benefits?)

Answer:
lessl likelyl tol causel EPS,l TDl orl NMS
mayl bel morel effectivel inl treatingl negl sxs
usedl tol tx:l acutel mania,l bipolar,l andl adjunctivel medl inl unipolarl depression;l canl alsol
helpl withl bordelrine,l PTSDl andl certainl ticl disorders



Q:l Whatl isl clozapine?l andl whatl arel itsl SEl profile?

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