Free Psychopharmacology Examination for Psychologists Practice Questions
250 free questions · Answer explanations · No signup required
View examination details, outline and sourcesLoading selected examination banks…
Sample Practice Questions
Try these 10 sample questions from the Psychopharmacology Examination for Psychologists practice bank. Each includes the answer and explanation. Continue with the interactive practice above to review the full question set.
1Prescription patterns summarized in APA's 2025 pharmacological-issues guidelines show that age and gender interact in who receives psychotropic treatment. Which pattern do the guidelines report?
- A. Psychotropic treatment is more common in female children and male adults
- B. Psychotropic treatment is more common in male children and male adults
- C. Psychotropic treatment is more common in female children and female adults
- D. Psychotropic treatment is more common in male children and female adults
Answer: D
Explanation: Guideline 3 states: "There is an interaction of age and gender such that treatment with psychotropics is more common in male children and female adults". The gender skew in utilization reverses between childhood and adulthood, so a clinician cannot assume a single direction of gender difference across the lifespan; the other three options describe patterns the guideline does not report.
Reference: APA Guidelines for Psychologists’ Involvement in Pharmacological Issues — Guideline 3, Rationale, item 2e (Differences in participation in treatment)
2Explaining how cocaine disrupts communication between neurons, a clinician first describes the normal job of synaptic transporter molecules. What is that job?
- A. Carrying released neurotransmitter across the synaptic gap to the receiving cell
- B. Bringing released neurotransmitter back into the neuron that released it
- C. Moving neurotransmitter-filled vesicles down the axon toward the terminal
- D. Converting the chemical signal at the dendrite back into an electrical one
Answer: B
Explanation: NIDA states: "Other molecules called transporters recycle neurotransmitters (that is, bring them back into the neuron that released them), thereby limiting or shutting off the signal between neurons." Transporters therefore end the signal by taking the transmitter back up into the neuron that released it, and this is the step cocaine interferes with. The neurotransmitter crosses the synapse on its own to reach receptors, and conversion back to an electrical signal happens in the receiving neuron, so those options describe other steps of transmission rather than the transporter's job.
Reference: NIDA, Drugs, Brains, and Behavior: The Science of Addiction - Drugs and the Brain — How does the brain work?
3An 82-year-old woman hospitalized for pneumonia becomes disoriented over a single afternoon, swinging between drowsiness and agitation, two days after an anticholinergic was added for bladder urgency; her daughter says she was managing her own finances last week. Which diagnosis best explains the change in cognition?
- A. Delirium superimposed on acute illness
- B. Dementia with Lewy bodies, now evident
- C. Alzheimer's disease unmasked by admission
- D. Post-stroke vascular dementia, early stage
Answer: A
Explanation: MedlinePlus defines the condition: "Delirium is sudden severe confusion due to rapid changes in brain function that can occur with physical or mental illness." It also notes that "Delirium involves a quick change between mental states (for example, from lethargy to agitation and back to lethargy)." Among listed causes are "Certain medicines such as pain medicines, sedatives, or anticholinergic medicines" and infections such as pneumonia. An abrupt, fluctuating change over hours in a woman who was cognitively intact a week ago, during pneumonia and after a new anticholinergic, is delirium. Dementia with Lewy bodies also fluctuates, but it is a progressive degenerative disease and would not appear de novo over one afternoon in a previously intact person; Alzheimer's and vascular dementia are likewise gradual.
Reference: MedlinePlus Medical Encyclopedia: Delirium — Introduction; Causes; Symptoms
4Three weeks after starting carbamazepine for bipolar disorder, a patient calls reporting fever, a sore throat, mouth ulcers, and new bruises on both shins. Which organ-system problem should prompt immediate physician evaluation in this case?
- A. Possible cardiac conduction disturbance, such as second- or third-degree AV heart block
- B. Possible blood dyscrasia, such as agranulocytosis or aplastic anemia from marrow injury
- C. Possible hepatic reaction, such as drug-induced hepatitis presenting with jaundice
- D. Possible hyponatremia from the syndrome of inappropriate antidiuretic hormone secretion
Answer: B
Explanation: Carbamazepine labeling tells patients to watch for early signs of a possible hematologic problem, including "fever, sore throat, rash, ulcers in the mouth, easy bruising, lymphadenopathy and petechial or purpuric hemorrhage", and says "they must report any occurrence immediately to a physician." Its boxed warning notes that "Aplastic anemia and agranulocytosis have been reported in association with the use of Tegretol". Fever, sore throat, mouth ulcers, and bruising together point to marrow suppression, so the patient needs prompt medical evaluation for a blood dyscrasia. Liver reactions show up as anorexia, nausea or vomiting, or jaundice. Conduction block and SIADH are real carbamazepine risks, but they do not explain this cluster.
Reference: Tegretol (carbamazepine) Prescribing Information — PRECAUTIONS, Information for Patients
5Before starting extended-release mixed amphetamine salts for a 19-year-old with newly diagnosed ADHD, which family history element does the prescribing information specifically direct the clinician to obtain as part of the cardiac assessment?
- A. Family history of sudden death or ventricular arrhythmia
- B. Family history of early-onset type 2 diabetes or obesity
- C. Family history of angle-closure glaucoma or cataracts
- D. Family history of epilepsy or febrile seizures in childhood
Answer: A
Explanation: The pretreatment screening section directs the prescriber to assess "for the presence of cardiac disease (i.e., perform a careful history, family history of sudden death or ventricular arrhythmia, and physical exam)". The reason is that "Sudden death has been reported in patients with structural cardiac abnormalities or other serious cardiac disease who were treated with CNS stimulants at the recommended ADHD dosage." A family history of diabetes matters for baseline glucose testing before atypical antipsychotics, and seizure history matters for drugs such as bupropion. Neither is the family history this label requires for the stimulant cardiac assessment.
Reference: ADDERALL XR (mixed amphetamine salts) extended-release capsules Prescribing Information (DailyMed) — Section 2.1 Pretreatment Screening
6A 78-year-old woman has grown withdrawn and apathetic, with poor appetite and weight loss, and her pulse is rapid and irregular. Her family assumes depression or early dementia. Which condition does NIDDK caution is sometimes mistaken for these in older adults?
- A. Underactive thyroid (hypothyroidism)
- B. Adrenal insufficiency (Addison's disease)
- C. Cortisol excess (Cushing's syndrome)
- D. Overactive thyroid (hyperthyroidism)
Answer: D
Explanation: NIDDK warns: "In older adults, hyperthyroidism is sometimes mistaken for depression or dementia." It adds that "Older adults may have different symptoms, such as loss of appetite or withdrawal from people, than younger adults with hyperthyroidism." Its symptom list includes "rapid or irregular heartbeat". Hypothyroidism instead causes a slowed heart rate, which does not fit this pulse finding.
Reference: NIDDK: Hyperthyroidism (Overactive Thyroid) — What are the symptoms of hyperthyroidism?
7During intake, a client discloses weekend use of gamma-hydroxybutyrate (GHB) bought at dance clubs. In NIDA's drug descriptions, GHB belongs to which pharmacological class?
- A. A central nervous system stimulant
- B. A central nervous system depressant
- C. A dissociative hallucinogenic drug
- D. An opioid-type analgesic drug
Answer: B
Explanation: NIDA states that "Gamma-hydroxybutyrate (GHB) is a depressant approved for use in the treatment of narcolepsy" and that it "may be misused for their euphoric and sedative effects". GHB is therefore classified as a CNS depressant. Dissociatives (e.g., PCP, ketamine), stimulants, and opioids are separate NIDA categories and do not describe GHB.
8A 22-year-old woman with major depressive disorder asks for bupropion to avoid sexual side effects; she was treated for bulimia nervosa three years ago and has been in remission since. What does the current bupropion labeling indicate?
- A. Bupropion may be started at usual doses because the eating disorder has been in remission for years
- B. Bupropion is contraindicated because a prior bulimia diagnosis is linked to a higher incidence of seizures
- C. Bupropion is acceptable provided the total daily dose never exceeds the 450 mg labeled maximum
- D. Bupropion is acceptable if the daily dose is capped at 75 mg throughout the course of treatment
Answer: B
Explanation: The label states: "WELLBUTRIN is contraindicated in patients with a current or prior diagnosis of bulimia or anorexia nervosa as a higher incidence of seizures was observed in such patients treated with WELLBUTRIN". The contraindication covers a prior diagnosis, so being in remission does not lift it. Capping the dose at the 450 mg maximum or at 75 mg (the cap used in moderate to severe hepatic impairment) does not remove the contraindication.
Reference: WELLBUTRIN (bupropion hydrochloride) tablets, FDA prescribing information — Section 4, Contraindications
9In a trial of a new anxiolytic, the treating clinicians and outcome raters know which capsule each participant receives, while participants get identical-appearing capsules and are never told their assignment. Under ICH E9 terminology, how is this level of blinding classified?
- A. Double-blind design
- B. Single-blind design
- C. Open-label design
- D. Double-dummy design
Answer: B
Explanation: ICH E9 defines the term: "In a single-blind trial the investigator and/or his staff are aware of the treatment but the subject is not, or vice versa." Here only the participants are unaware, so the trial is single-blind. It is not double-blind, because in that design "neither the subject nor any of the investigator or sponsor staff involved in the treatment or clinical evaluation of the subjects are aware of the treatment received." It is not open-label, where "the identity of treatment is known to all." Double-dummy is a way of keeping a double blind when two treatments look different, not a level of blinding.
Reference: FDA Guidance for Industry: E9 Statistical Principles for Clinical Trials (ICH) — Design Techniques to Avoid Bias: Blinding
10At one visit, an individual practitioner wants to issue a stable ADHD patient several dated prescriptions for a Schedule II stimulant. Under DEA regulations, what total supply may these multiple prescriptions authorize?
- A. Up to a 30-day supply
- B. Up to a 60-day supply
- C. Up to a 90-day supply
- D. Up to a 180-day supply
Answer: C
Explanation: 21 CFR 1306.12(b)(1) provides that "An individual practitioner may issue multiple prescriptions authorizing the patient to receive a total of up to a 90-day supply of a Schedule II controlled substance", provided each is issued for a legitimate medical purpose and carries the earliest fill date. Because refilling a Schedule II prescription is prohibited, multiple prescriptions are the only route to a longer supply, capped at 90 days.
Reference: 21 CFR Part 1306 — Prescriptions (eCFR) — 21 CFR 1306.12(b)(1)
Topics in this practice bank
These topics describe the available practice for Psychopharmacology Examination for Psychologists. Review the examination outline and its sources for scope and allocation details.
Content Area 1: Integrating Clinical Psychopharmacology with the Practice of Psychology — Refers to integrating clinical psychopharmacology with the practice of psychology
- Knowledge of biopsychosocial variables as determinants of medication utilization and effects (e.g., age, gender, family history, patient belief systems/ culture, economics/ poverty, social support, current environmental circumstances).
- Knowledge of limitations and benefits, patient perceptions (including help-seeking attitudes), and treatment expectations regarding psychopharmacological and psychological interventions as sole, additive, or interactive treatments for given disorders and functional impairments.
- Knowledge of practitioner-patient partnership for case and medication management, including the impact on patient education, medication adherence, the effectiveness of treatment, adverse effects and response to side effects, and implications for the relationship when psychosocial and pharmacological interventions are utilized (e.g., ethnicity/culture, sexual orientation, gender identity, socio-economic factors, religion, refugee status).
- Knowledge of the development and implementation of a coherent and organized integrated treatment plan of psychosocial, cultural (including the participation of traditional healers when appropriate), and pharmacological interventions with attention to comorbidities, as well as evidence-based developments in psychotherapy and pharmacotherapy.
Content Area 2: Neuroscience — Refers to the anatomy, physiology, and biochemistry of the nervous system and its interfaces with other major body systems.
- Knowledge of cellular and molecular nervous system biology and regulatory processes (e.g., neurotransmitter and neuromodulator systems, up and down-regulation, tolerance/cross-tolerance) needed to understand the pharmacological effect of medications.
- Knowledge of the structure and function of the central and peripheral nervous systems.
- Knowledge of neurodevelopment and neuroplasticity.
- Knowledge of the major neuronal pathways and their functions, and associated messenger systems.
Content Area 3: Nervous System Pathology — Refers to disorders of the nervous system resulting in abnormal function or behavioral/ mood disruption. Includes biochemical, structural (congenital or acquired), or neurophysiological abnormalities and their impact on other body systems.
- Knowledge of etiological factors and diagnosis of dementia, delirium, and other cognitive and neurological disorders.
- Knowledge of etiological factors and diagnosis of chronic pain, including headache (e.g., migrainous vs. non-migrainous headache), neuropathic pain, fibromyalgia; and the role of the CNS in pain experience and management.
- Knowledge of etiological factors and diagnosis of sleep disorders.
- Knowledge of common idiopathic movement disorders, their etiological factors, signs, symptoms, and diagnosis (e.g., Parkinson’s, Huntington’s, Tourette’s syndrome).
- Knowledge of common iatrogenic or drug-induced movement disorders, their etiological factors, signs, symptoms, and diagnosis (e.g., extrapyramidal symptoms, dystonias, dyskinesias, akathisia, Dystonic Tremors (DTs)).
- Knowledge of etiological factors and categories of seizure disorders.
- Knowledge of traumatic brain injury and post-concussive or post-concussion syndrome and its impact on prescriptive decisions.
- Knowledge of nervous system pathology (e.g., multiple sclerosis, infectious diseases, exposure to environmental neurotoxins, neoplasms, intellectual/developmental disabilities).
- Knowledge of basic indications for neurodiagnostic imaging and testing (e.g., EEG, CT, MRI, neuropsychological).
Content Area 4: Physiology and Pathophysiology — Refers to normal physiology and pathophysiology across the life span, and their impact on psychological functioning and psychopharmacology.
- Knowledge of indications for referral to other health care providers for assessment or treatment when organ system pathology is indicated.
- Knowledge at a functional level of cardiovascular system physiology and pathophysiology across the life span (e.g., rhythm and rate disorders such as prolonged QT interval), and their relationship to psychopharmacology and psychopathology (e.g., blood pressure changes secondary to psychotropic medication; mitral valve prolapse related to panic disorder).
- Knowledge at a functional level of pulmonary system physiology and pathophysiology across the life span, and their relationships to psychopharmacology and psychopathology (e.g., beta blockers and asthma, respiratory suppression with CNS depressants).
- Knowledge of etiological factors and diagnosis of central nervous system vascular disorders (e.g., cerebral vascular accidents, transient ischemic attacks).
- Knowledge at a functional level of renal/genitourinary system physiology and pathophysiology across the life span, and their relationships to psychopharmacology and psychopathology (e.g., the effect of psychotropic substances on urinary/sexual functioning; role in excretion of wastes and medications; valproic acid and polycystic ovary syndrome (PCOS); lithium and renal functioning).
Content Area 5: Biopsychosocial and Pharmacologic Assessment and Monitoring — Refers to a range of biopsychosocial (psychological, neurological, behavioral, physical, biomedical) and pharmacologic assessment techniques and procedures for baseline and ongoing evaluation of the individual’s physical and psychological health status as well as the assessment of therapeutic efficacy, adverse effects, contraindications for drug usage, drug interactions, and appropriateness for medication continuation, modification, or discontinuation.
- Knowledge of individual and family history-taking procedures and psychological assessments that provide information relevant to prescribing (e.g., review of systems, dietary habits, mental status, behavioral observations, developmental history, social history, academic history, family medical and psychiatric history (including knowledge of diversity-related variations in the incidence/ prevalence of disorders), history of sexually transmitted disease and history of the general level of functioning).
- Knowledge of basic physical and neurological examination procedures (e.g., history and physical examination (HPE); review of systems (ROS)) and variations in these procedures for special populations (e.g., ethnicity and estimated glomerular filtration rate (EGFR)).
- Knowledge of appropriate laboratory tests and assessment procedures before prescribing particular medications (e.g., the implication of disease states, gender, ethnicity, sample timing, and potential effects of medications on those values) and ongoing during treatment (e.g., therapeutic drug monitoring (TDM) for lithium blood levels, white blood cell monitoring with clozapine use).
- Knowledge of behavioral assessment methods (e.g., rating scales, direct observation of behaviors, parent/ teacher/self-report) at baseline and ongoing monitoring for therapeutic effectiveness, quality of life, and adverse effects of psychopharmacological agents (e.g., akathisia with antipsychotics and SSRIs; rating scales for ADHD; Mini Mental Status Examination (MMSE) for cognitive function; Clinical Global Impression (CGI) scale for global response to treatment).
Content Area 6: Differential Diagnosis — Refers to the use of comprehensive diagnostic information about a patient to establish an accurate diagnosis from among possible medical and psychological diagnoses to select appropriate treatment modalities and determine the appropriateness of referral to other health care providers.
- Knowledge of medical disorders and their most common symptoms that may also present with psychological symptoms (e.g., ADHD versus PKU versus autism, anxiety versus Graves’ disease, dementia versus depression in the elderly; depression as a primary disorder vs. a prodromal sign of underlying cancer; personality changes in the elderly vs. dementia).
- Knowledge of psychological signs and symptoms (e.g., mental status changes, memory dysfunction, depression, psychosis) secondary to substances of abuse, prescribed and over-the-counter (OTC) medications, most commonly used herbal remedies that have psychological effects, and dietary supplements.
- Knowledge of the psychopharmacological treatment implications related to mental health disorders with multiple symptoms (e.g., one disorder with multiple symptoms vs. comorbid disorders with related symptoms: major depressive disorder with psychotic features vs. major depressive disorder and schizophrenia; anxious depression vs. anxiety disorder and dysthymia; bipolar vs. psychotic depression; behavioral health disorders and substance use disorders).
- Knowledge of iatrogenic effects of medication versus primary symptoms of disease course (e.g., akathisia versus anxiety; anticholinergic effects versus dementia; medication-induced tremor versus idiopathic movement disorders).
Content Area 7: Pharmacology — Refers to the interactions of drugs with biophysiological systems; encompasses pharmacokinetics, pharmacodynamics, pharmacogenetics, and the epidemiology of various medications such as psychotropics, adjunctive agents, and other medications used in the practice of medicine, as well as substances of abuse, OTC products, and food and dietary supplements. The influence of cultural/ethnic factors, environmental factors, and responses of special populations are considered.
- Knowledge of drug classifications for psychotropic and adjunctive medications (e.g., stimulants, sedatives, antidepressants, anticholinergics), major drug categories used to treat common medical disorders (e.g., antibiotics), OTC medications, herbals, and substances of abuse.
- Knowledge of pharmacokinetic parameters (e.g., absorption, distribution, metabolism, and elimination) and how each phase affects drug action (e.g., delayed-release preparations, routes of administration, area under the curve, lipophilicity and drug transit across membrane barriers, CYP enzymes, drug/drug and drug/food interactions, routes of clearance).
- Knowledge of pharmacodynamic changes caused by medications (receptor up/down regulation; transcription).
- Knowledge of the importance of biological half-life in determining steady state drug concentrations, dosing schedules, accumulation, and toxicity.
- Knowledge of drug properties and characteristics (e.g., therapeutic index, therapeutic blood levels/ prescription doses, potency, bioavailability, efficacy, cognitive and behavioral manifestations of toxicity, dose response relationships).
- Knowledge of types of drugs/receptor interactions (e.g., direct and indirect agonists, antagonists, partial agonists, inverse agonists, competitive vs. non-competitive antagonism and agonism).
- Knowledge of the relationship between neurotransmitters and their receptor targets and the behavioral effects of stimulation vs. inhibition (e.g., 5HT1A and anxiety, beta blockers and performance anxiety, D2 and psychosis; histamine and sedation; ACh and memory).
- Knowledge of the mechanism of action of common therapeutic agents (e.g., receptor stimulation/inhibition; receptor up/down regulation; tolerance, dependence, and withdrawal).
- Knowledge of the theoretical relationship between neurotransmitter systems and psycho-pathological conditions (e.g., serotonin and norepinephrine in depression, dopamine in psychosis and substance abuse; dopamine in Parkinson’s disease; acetylcholine in Alzheimer’s disease).
- Knowledge of the factors (e.g., biological, ethnic, pharmacodynamic, genetic, pharmacokinetic) related to intra- and inter-individual responses to medications (e.g., variation of blood levels to the same dose across individuals, change in responsiveness within the same individual across administrations of same drug [e.g., pregnancy, obesity, age]).
- Knowledge of drug-induced disease, dysfunction, and adverse reactions (e.g., hepatotoxicity, agranulocytosis, dystonias).
Content Area 8: Clinical Psychopharmacology — Refers to the application of pharmacology to the management of psychological/behavioral disorders. This includes indications, contradictions, dosing, adverse effects and toxicities of psychotropic and adjunctive medications, interactions with other medications (including other drugs used in medicine for recreational purposes, and available for OTC purchase) as well as the management of adverse reactions, overdoses, and toxicities.
- Knowledge of indications and contraindications for various psychotropic medications, including use of multiple medications both on and off label.
- Knowledge of decision-making strategies for psychotropic medication selection (e.g., risk-benefit analysis, practice guidelines, genetics, ethnicity, cost, pregnancy, disease status, limitations of current diagnostic systems [e.g., DSM, ICD]).
- Knowledge of dosing, time course of therapeutic action, and adverse effects of medication based on patient factors (e.g., weight, gender, ethnicity, culture, age, trauma, pregnancy, concurrent disease).
- Knowledge of dosing strategies (e.g., augmentation, titration, cross taper, discontinuation).
- Knowledge of common signs and symptoms of drug toxicity and the management of adverse reactions to drugs (e.g., referral for appropriate medical care, use of appropriate medications).
- Knowledge of the management of at-risk patients (e.g., relapse prevention, adherence, suicide prevention, patients seeking medication inappropriate or inconsistent with treatment plan).
- Knowledge of potential adverse psychological and physiological signs of drugs used for common medical conditions (e.g., steroids, beta blockers, antibiotics, antivirals), OTCs, and herbals/dietary supplements.
- Knowledge of psychological and physiological signs of common recreational substances and the management of intoxication or addiction, including strategies for assisted withdrawal, maintenance, and relapse prevention.
- Knowledge of how to recognize and manage tolerance, cross-tolerance, dependence, and abstinence syndromes, sensitization/cross-sensitization with respect to specific medications.
- Knowledge of the patient factors (e.g., culture, literacy, stage of change) that need to be considered when informing patients about drug utilization, risks, benefits, potential complications, and alternatives to pharmacotherapy.
Content Area 9: Research — Refers to the methodology, standards, and conduct of research on psychoactive substances. The knowledge base facilitates research design and implementation, accurate data interpretation and communication, effective utilization of findings, the accumulation of scientific knowledge, and the improvement of the practice of clinical psychology.
- Knowledge of research designs and analytic techniques used in psychopharmacological research (e.g., open label, single vs double blind, random assignment, placebo control, drug washout, dose response relationships, intent-to-treat analyses, within-subject and group designs, concurrent administration of other drugs, FDA drug development process).
- Knowledge of how to critically review clinical research data including non-evidence-based therapies and emerging research methodologies and use the information for making treatment decisions (e.g., Number needed to treat (NNT), Number needed to harm (NNH), Odds ratio (OR), Risk ratio (RR), effect size).
- Knowledge of influential, non-industry sponsored multi-site research studies relating to psychopharmacology (e.g., CATIE, STAR-D, CUTLASS, MTA).
- Knowledge of evidence-based research regarding complementary and alternative medicines (e.g., Omega-3, folate, dehydroepiandrosterone (DHEA), St. John’s Wort, melatonin).
Content Area 10: Professional, Legal, Ethical, and Interprofessional Issues — Refers to the knowledge of ethics, standards of care, laws, and regulations relevant to the practice of psychology involving psychopharmacology.
- Knowledge of relevant legal and ethical codes and standards that pertain to pharmacological practice; and laws and statutes for prescribing psychotropic medications (e.g., DEA regulations, telehealth).
- Knowledge of practice guidelines and standards of care for prescribing psychotropic medications (including a relationship with referring psychologist).
- Knowledge of patients’ rights related to medication treatments and therapy (e.g., informed consent, right to refuse treatment, right to treatment within the least restrictive environment, inappropriate psychotropic restraints, duty to warn, privileged communication, alternative decision maker, living will, durable power of attorney, advance directives).
- Knowledge of ethical issues regarding relationships with pharmaceutical companies (e.g., acceptance of gifts and samples, revealing sources of funding and affiliations, interactions with pharmaceutical reps).
How to use these free practice questions
Choose an answer, check the explanation, and review your progress by chapter. Practice questions and explanations are free to access without signing up.
These are independent study questions, not actual examination items. For examination requirements and official information, view Psychopharmacology Examination for Psychologists details.