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Question 1
Correct
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Which drug was introduced into clinical practice by Kane?
Your Answer: Clozapine
Explanation:Clozapine has a unique past, having been initially utilized in Europe during the early 1970s. Its effectiveness was notable, particularly due to its lack of causing EPSE’s. However, its popularity declined after several instances of agranulocytosis. In 1988, Kane conducted a study that demonstrated its safe use with proper blood monitoring, leading to its introduction in both the UK and the US.
A Historical Note on the Development of Zimelidine, the First Selective Serotonin Reuptake Inhibitor
In 1960s, evidence began to emerge suggesting a significant role of serotonin in depression. This led to the development of zimelidine, the first selective serotonin reuptake inhibitor (SSRI). Zimelidine was derived from pheniramine and was marketed in Europe in 1982. However, it was removed from the market in 1983 due to severe side effects such as hypersensitivity reactions and Guillain-Barre syndrome.
Despite its short-lived availability, zimelidine paved the way for the development of other SSRIs such as fluoxetine, which was approved by the FDA in 1987 and launched in the US market in 1988 under the trade name Prozac. The development of SSRIs revolutionized the treatment of depression and other mood disorders, providing a safer and more effective alternative to earlier antidepressants such as the tricyclics and MAO inhibitors.
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This question is part of the following fields:
- Psychopharmacology
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Question 2
Correct
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Which of the following is most likely to result from use of carbamazepine?
Your Answer: Leucopenia
Explanation:Carbamazepine use can result in leucopenia, which is a reduction in white blood cell count, affecting 1 in 10 individuals. Although other side effects can occur with carbamazepine, they are rare of very rare. The decrease in WBC is believed to be due to the inhibition of colony-stimulating factor in the bone marrow. However, the co-administration of lithium, which stimulates colony-stimulating factor, may potentially reverse the effects of carbamazepine (Daughton, 2006).
Carbamazepine: Uses, Mechanism of Action, Contraindications, Warnings, and Side-Effects
Carbamazepine, also known as Tegretol, is a medication commonly used in the treatment of epilepsy, particularly partial seizures. It is also used for neuropathic pain, bipolar disorder, and other conditions. The drug works by binding to sodium channels and increasing their refractory period.
However, carbamazepine has notable contraindications, including a history of bone marrow depression and combination with monoamine oxidase inhibitors (MAOIs). It also carries warnings for serious dermatological reactions such as toxic epidermal necrolysis (TEN) and Stevens Johnson syndrome.
Common side-effects of carbamazepine include leucopenia, ataxia, dizziness, somnolence, vomiting, nausea, urticaria, and fatigue. Other side-effects include thrombocytopenia, eosinophilia, oedema, fluid retention, weight increase, hyponatraemia, and blood osmolarity decreased due to an antidiuretic hormone (ADH)-like effect, leading in rare cases to water intoxication accompanied by lethargy, vomiting, headache, confusional state, neurological disorders, diplopia, accommodation disorders (e.g. blurred vision), and dry mouth.
In summary, carbamazepine is a medication with multiple uses, but it also carries significant contraindications, warnings, and side-effects that should be carefully considered before use.
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This question is part of the following fields:
- Psychopharmacology
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Question 3
Correct
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Which of the following factors is believed to have no negative effect on sexual function?
Your Answer: Lurasidone
Explanation:Antipsychotics and Sexual Dysfunction: Causes, Risks, and Management
Sexual dysfunction is a common side effect of antipsychotic medication, with the highest risk associated with risperidone and haloperidol due to their effect on prolactin levels. Clozapine, olanzapine, quetiapine, aripiprazole, asenapine, and lurasidone are associated with lower rates of sexual dysfunction. The Arizona Sexual Experiences Scale (ASEX) can be used to measure sexual dysfunction before and during treatment. Management options include excluding other causes, watchful waiting, dose reduction, switching to a lower risk agent, adding aripiprazole, considering an antidote medication, of using sildenafil for erectile dysfunction. It is important to address sexual dysfunction to improve quality of life and medication adherence.
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This question is part of the following fields:
- Psychopharmacology
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Question 4
Correct
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What factors can cause an increase in the levels of lamotrigine?
Your Answer: Valproate
Explanation:This question is quite challenging, and it’s understandable if you didn’t get the answer right. Even healthcare professionals like consultants and pharmacists may struggle with this. However, for the record, the levels of lamotrigine can be increased by sertraline and valproate.
Lamotrigine: An Anticonvulsant Drug for Epilepsy, Bipolar Disorder, and Depression
Lamotrigine is a medication that belongs to the class of anticonvulsants. It is commonly used in the treatment of epilepsy, bipolar disorder, and depression. Epilepsy is a neurological disorder characterized by recurrent seizures, while bipolar disorder is a mental illness that causes extreme mood swings. Depression, on the other hand, is a mood disorder that affects a person’s thoughts, feelings, and behavior.
Lamotrigine works by stabilizing the electrical activity in the brain, which helps to prevent seizures and mood swings. It is often used as a first-line treatment for epilepsy and is effective in reducing the frequency and severity of seizures. In bipolar disorder, lamotrigine is used to prevent episodes of mania and depression. It can also be used as an add-on therapy for depression, particularly in cases where other antidepressants have not been effective.
Overall, lamotrigine is a versatile medication that can be used to treat a range of neurological and psychiatric conditions. It is generally well-tolerated and has few side effects, making it a popular choice for many patients. However, as with all medications, it is important to discuss the risks and benefits with your healthcare provider before starting treatment.
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This question is part of the following fields:
- Psychopharmacology
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Question 5
Correct
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Which type of depot injection is the most probable cause of the 23-year-old male's sedation, dysarthria, and ataxia that occurred 30 minutes after administration?
Your Answer: Olanzapine embonate
Explanation:The presentation is indicative of post-injection syndrome related to olanzapine embonate.
, coma, respiratory depression (rare)
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This question is part of the following fields:
- Psychopharmacology
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Question 6
Correct
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What antidepressant belongs to the NaSSA classification?
Your Answer: Mirtazapine
Explanation:Mirtazapine and Mianserin are significant NaSSA’s (Noradrenergic and specific serotonergic antidepressants) that function by blocking adrenergic and serotonergic receptors. In contrast to the majority of antidepressants, they do not impact the reuptake of serotonin.
Mechanisms of Action of Different Drugs
Understanding the mechanisms of action of different drugs is crucial for medical professionals. It is a common topic in exams and can earn easy marks if studied well. This article provides a list of drugs and their mechanisms of action in different categories such as antidepressants, anti dementia drugs, mood stabilizers, anxiolytic/hypnotic drugs, antipsychotics, drugs of abuse, and other drugs. For example, mirtazapine is a noradrenaline and serotonin specific antidepressant that works as a 5HT2 antagonist, 5HT3 antagonist, H1 antagonist, alpha 1 and alpha 2 antagonist, and moderate muscarinic antagonist. Similarly, donepezil is a reversible acetylcholinesterase inhibitor used as an anti dementia drug, while valproate is a GABA agonist and NMDA antagonist used as a mood stabilizer. The article also explains the mechanisms of action of drugs such as ketamine, phencyclidine, buprenorphine, naloxone, atomoxetine, varenicline, disulfiram, acamprosate, and sildenafil.
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This question is part of the following fields:
- Psychopharmacology
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Question 7
Correct
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Which of the following factors does not increase the risk of QTc prolongation?
Your Answer: Male gender
Explanation:Some additional risk factors for QTc prolongation include being female and having a slow heart rate (bradycardia).
Amantadine and QTc Prolongation
Amantadine is a medication used to treat Parkinson’s disease and influenza. It has been associated with QTc prolongation, which can increase the risk of Torsades de points. Therefore, caution should be exercised when prescribing amantadine to patients with risk factors for QT prolongation. If a patient is already taking amantadine and develops a prolonged QTc interval, the medication should be discontinued and an alternative treatment considered. It is important to monitor the QTc interval in patients taking amantadine, especially those with risk factors for QT prolongation.
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This question is part of the following fields:
- Psychopharmacology
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Question 8
Correct
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Choose the medication with the most extended half-life:
Your Answer: Nitrazepam
Explanation:Benzodiazepines are a class of drugs commonly used to treat anxiety and sleep disorders. It is important to have a working knowledge of the more common benzodiazepines and their half-life. Half-life refers to the amount of time it takes for half of the drug to be eliminated from the body.
Some of the more common benzodiazepines and their half-life include diazepam with a half-life of 20-100 hours, clonazepam with a half-life of 18-50 hours, chlordiazepoxide with a half-life of 5-30 hours, nitrazepam with a half-life of 15-38 hours, temazepam with a half-life of 8-22 hours, lorazepam with a half-life of 10-20 hours, alprazolam with a half-life of 10-15 hours, oxazepam with a half-life of 6-10 hours, zopiclone with a half-life of 5-6 hours, zolpidem with a half-life of 2 hours, and zaleplon with a half-life of 2 hours. Understanding the half-life of these drugs is important for determining dosages and timing of administration.
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This question is part of the following fields:
- Psychopharmacology
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Question 9
Incorrect
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On which of the following does CYP2D6 have a notable impact in terms of metabolism?
Your Answer: Bupropion
Correct Answer: Olanzapine
Explanation:The Cytochrome P450 system is a group of enzymes that metabolize drugs by altering their functional groups. The system is located in the liver and small intestine and is involved in drug interactions through enzyme induction of inhibition. Notable inducers include smoking, alcohol, and St John’s Wort, while notable inhibitors include grapefruit juice and some SSRIs. CYP2D6 is important due to genetic polymorphism, and CYP3A4 is the most abundant subfamily and is commonly involved in interactions. Grapefruit juice inhibits both CYP1A2 and CYP3A4, while tobacco smoking induces CYP1A2. The table summarizes the main substrates, inhibitors, and inducers for each CYP enzyme.
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This question is part of the following fields:
- Psychopharmacology
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Question 10
Correct
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What is the mechanism of action of sildenafil?
Your Answer: Inhibition of phosphodiesterase
Explanation:Nitrous oxide functions as a vasodilator during penile erection by diffusing through the muscle cell membrane and binding to guanylyl cyclase. This enzyme catalyzes the conversion of GTP to cyclic GMP, which activates a cGMP-dependent protein kinase. This kinase stimulates the uptake of calcium by the endoplasmic reticulum of the muscle cell, leading to muscle relaxation and vasodilation, resulting in an erection.
To end the erection, cGMP is converted into GMP by a specific phosphodiesterase (PDE). There are ten families of PDEs, with PDE5 being the primary PDE found in vascular smooth muscle. Sildenafil (Viagra) is a specific inhibitor of PDE5, blocking the breakdown of cGMP and prolonging the effects of cGMP, thereby prolonging the erection.
Mechanisms of Action of Different Drugs
Understanding the mechanisms of action of different drugs is crucial for medical professionals. It is a common topic in exams and can earn easy marks if studied well. This article provides a list of drugs and their mechanisms of action in different categories such as antidepressants, anti dementia drugs, mood stabilizers, anxiolytic/hypnotic drugs, antipsychotics, drugs of abuse, and other drugs. For example, mirtazapine is a noradrenaline and serotonin specific antidepressant that works as a 5HT2 antagonist, 5HT3 antagonist, H1 antagonist, alpha 1 and alpha 2 antagonist, and moderate muscarinic antagonist. Similarly, donepezil is a reversible acetylcholinesterase inhibitor used as an anti dementia drug, while valproate is a GABA agonist and NMDA antagonist used as a mood stabilizer. The article also explains the mechanisms of action of drugs such as ketamine, phencyclidine, buprenorphine, naloxone, atomoxetine, varenicline, disulfiram, acamprosate, and sildenafil.
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This question is part of the following fields:
- Psychopharmacology
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Question 11
Correct
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What is a significant byproduct of clozapine metabolism?
Your Answer: N-desmethylclozapine
Explanation:Clozapine is an atypical antipsychotic drug that acts as an antagonist at various receptors, including dopamine, histamine, serotonin, adrenergic, and cholinergic receptors. It is mainly metabolized by CYP1A2, and its plasma levels can be affected by inducers and inhibitors of this enzyme. Clozapine is associated with several side effects, including drowsiness, constipation, weight gain, and hypersalivation. Hypersalivation is a paradoxical side effect, and its mechanism is not fully understood, but it may involve clozapine agonist activity at the muscarinic M4 receptor and antagonist activity at the alpha-2 adrenoceptor. Clozapine is also associated with several potentially dangerous adverse events, including agranulocytosis, myocarditis, seizures, severe orthostatic hypotension, increased mortality in elderly patients with dementia-related psychosis, colitis, pancreatitis, thrombocytopenia, thromboembolism, and insulin resistance and diabetes mellitus. The BNF advises caution in using clozapine in patients with prostatic hypertrophy, susceptibility to angle-closure glaucoma, and adults over 60 years. Valproate should be considered when using high doses of clozapine, plasma levels > 0.5 mg/l, of when the patient experiences seizures. Myocarditis is a rare but potentially fatal adverse event associated with clozapine use, and its diagnosis is based on biomarkers and clinical features. The mortality rate of clozapine-induced myocarditis is high, and subsequent use of clozapine in such cases leads to recurrence of myocarditis in most cases.
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This question is part of the following fields:
- Psychopharmacology
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Question 12
Correct
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For a 45-year-old man who has not seen improvement with two different antidepressants, what combination of medications would you recommend?
Your Answer: Mirtazapine and sertraline
Explanation:The cautious use of combined antidepressants can be considered for depression management, taking into account their mechanism of action. NICE suggests the combination of mirtazapine and SSRI for treatment-resistant depression. However, other combinations should be avoided due to the risk of interaction.
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This question is part of the following fields:
- Psychopharmacology
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Question 13
Incorrect
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A 32-year-old female patient with a diagnosis of alcohol use disorder is interested in decreasing her alcohol intake, but acknowledges that complete abstinence may not be achievable. What treatment options are appropriate in this case?
Your Answer: Naltrexone
Correct Answer: Nalmefene
Explanation:Alcohol Dependence Treatment Options
Nalmefene has recently been approved for reducing alcohol consumption in alcohol-dependent patients who have a high risk of drinking but do not experience physical withdrawal symptoms and do not require immediate detoxification.
Acamprosate, when used in conjunction with counseling, may help maintain abstinence in alcohol-dependent patients who experience strong cravings.
Bupropion hydrochloride, which has been used as an antidepressant, has been found to be effective in maintaining smoking cessation.
Disulfiram, when consumed with alcohol, causes an extremely unpleasant systemic reaction due to the accumulation of acetaldehyde.
Naltrexone, an opioid-receptor antagonist, may be used to treat alcohol dependence after successful withdrawal.
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This question is part of the following fields:
- Psychopharmacology
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Question 14
Correct
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What is the half-life of fluoxetine in the body?
Your Answer: 4-6 days
Explanation:Fluoxetine has the longest half life among the commonly used SSRIs, lasting four to six days. Its active metabolite, norfluoxetine, remains active for four to 16 days. This information is important when discontinuing of switching SSRIs.
For instance, if a patient is discontinuing an SSRI with a shorter half life, such as paroxetine, they may experience SSRI discontinuation syndrome. To avoid this, they can switch to fluoxetine before tapering off the antidepressant.
When cross-titrating from fluoxetine to another antidepressant, the longer half life means that the drug needs to be withdrawn and a longer period allowed for levels in the body to decrease. The recommended time to start a new antidepressant after withdrawing fluoxetine varies depending on the drug, such as waiting five to six weeks before starting an MAOI.
The incorrect answers are:
– Paroxetine has an elimination half life of 24 hours
– Sertraline has an elimination half life of 26 hours
– Escitalopram has an elimination half life of 30 hours
– Citalopram has an elimination half life of 33 hours. -
This question is part of the following fields:
- Psychopharmacology
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Question 15
Correct
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What is the current licensing of asenapine, a psychotropic medication that was introduced in the UK in 2012?
Your Answer: Moderate to severe manic episodes related to bipolar affective disorder
Explanation:Asenapine is an unconventional antipsychotic that binds to D2, 5HT2A, 5HT2C, and alpha 1 and 2 adrenergic receptors. Originally intended for individuals with schizophrenia and bipolar affective disorder, it is presently authorized in the UK solely for managing moderate to severe manic episodes.
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This question is part of the following fields:
- Psychopharmacology
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Question 16
Correct
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Which medication is linked to priapism?
Your Answer: Trazodone
Explanation:The alpha adrenergic antagonism caused by Trazodone can lead to priapism. Trazodone is an antidepressant that is similar to tricyclics and is commonly prescribed for depression with anxiety and the need for sedation.
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This question is part of the following fields:
- Psychopharmacology
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Question 17
Incorrect
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Which tricyclic antidepressant has been demonstrated to have higher toxicity compared to others?
Your Answer: Amoxapine
Correct Answer: Dothiepin
Explanation:Tricyclic Antidepressants: Uses, Types, and Side-Effects
Tricyclic antidepressants (TCAs) are a type of medication used for depression and neuropathic pain. However, due to their side-effects and toxicity in overdose, they are not commonly used for depression anymore. TCAs can be divided into two types: first generation (tertiary amines) and second generation (secondary amines). The secondary amines have a lower side effect profile and act primarily on noradrenaline, while the tertiary amines boost serotonin and noradrenaline.
Some examples of secondary amines include desipramine, nortriptyline, protriptyline, and amoxapine. Examples of tertiary amines include amitriptyline, lofepramine, imipramine, clomipramine, dosulepin (dothiepin), doxepin, trimipramine, and butriptyline. Common side-effects of TCAs include drowsiness, dry mouth, blurred vision, constipation, and urinary retention.
Low-dose amitriptyline is commonly used for neuropathic pain and prophylaxis of headache. Lofepramine has a lower incidence of toxicity in overdose. However, amitriptyline and dosulepin (dothiepin) are considered the most dangerous in overdose. It is important to consult with a healthcare provider before taking any medication and to follow their instructions carefully.
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This question is part of the following fields:
- Psychopharmacology
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Question 18
Correct
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What medication acts as both a serotonin and noradrenaline reuptake inhibitor?
Your Answer: Duloxetine
Explanation:SNRIs include duloxetine and venlafaxine.
Antidepressants: Mechanism of Action
Antidepressants are a class of drugs used to treat depression and other mood disorders. The mechanism of action of antidepressants varies depending on the specific drug. Here are some examples:
Mirtazapine is a noradrenaline and serotonin specific antidepressant (NaSSa). It works by blocking certain receptors in the brain, including 5HT-1, 5HT-2, 5HT-3, and H1 receptors. It also acts as a presynaptic alpha 2 antagonist, which stimulates the release of noradrenaline and serotonin.
Venlafaxine and duloxetine are both serotonin and noradrenaline reuptake inhibitors (SNRIs). They work by blocking the reuptake of these neurotransmitters, which increases their availability in the brain.
Reboxetine is a noradrenaline reuptake inhibitor (NRI). It works by blocking the reuptake of noradrenaline, which increases its availability in the brain.
Bupropion is a noradrenaline and dopamine reuptake inhibitor (NDRI). It works by blocking the reuptake of these neurotransmitters, which increases their availability in the brain.
Trazodone is a weak serotonin reuptake inhibitor (SRI) and 5HT agonist. It works by increasing the availability of serotonin in the brain.
St John’s Wort is a natural supplement that has been used to treat depression. It has a weak monoamine oxidase inhibitor (MAOI) effect and a weak SNRI effect.
In summary, antidepressants work by increasing the availability of certain neurotransmitters in the brain, such as serotonin, noradrenaline, and dopamine. The specific mechanism of action varies depending on the drug.
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This question is part of the following fields:
- Psychopharmacology
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Question 19
Correct
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Which symptom is typically absent in cases of neuroleptic malignant syndrome?
Your Answer: Bradycardia
Explanation:Serotonin Syndrome and Neuroleptic Malignant Syndrome are two conditions that can be difficult to differentiate. Serotonin Syndrome is caused by excess serotonergic activity in the CNS and is characterized by neuromuscular abnormalities, altered mental state, and autonomic dysfunction. On the other hand, Neuroleptic Malignant Syndrome is a rare acute disorder of thermoregulation and neuromotor control that is almost exclusively caused by antipsychotics. The symptoms of both syndromes can overlap, but there are some distinguishing clinical features. Hyper-reflexia, ocular clonus, and tremors are more prominent in Serotonin Syndrome, while Neuroleptic Malignant Syndrome is characterized by uniform ‘lead-pipe’ rigidity and hyporeflexia. Symptoms of Serotonin Syndrome usually resolve within a few days of stopping the medication, while Neuroleptic Malignant Syndrome can take up to 14 days to remit with appropriate treatment. The following table provides a useful guide to the main differentials of Serotonin Syndrome and Neuroleptic Malignant Syndrome.
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This question is part of the following fields:
- Psychopharmacology
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Question 20
Incorrect
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What is the presumed cause of the sexual dysfunction associated with SSRIs?
Your Answer: 5-HT3 antagonism
Correct Answer: 5-HT2 agonism
Explanation:The inhibition of sexual behavior is caused by the activation of 5-HT2 receptors. However, this effect can be reversed by using 5-HT2 antagonists like cyproheptadine and 5-HT1a agonists like buspirone. These drugs are effective in treating sexual dysfunction caused by selective serotonin reuptake inhibitors (SSRIs).
Antidepressants can cause sexual dysfunction as a side-effect, although the rates vary. The impact on sexual desire, arousal, and orgasm can differ depending on the type of antidepressant. It is important to rule out other causes and consider non-pharmacological strategies such as reducing the dosage of taking drug holidays. If necessary, switching to a lower risk antidepressant of using pharmacological options such as phosphodiesterase inhibitors of mirtazapine augmentation can be considered. The Maudsley Guidelines 14th Edition provides a helpful table outlining the risk of sexual dysfunction for different antidepressants.
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This question is part of the following fields:
- Psychopharmacology
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Question 21
Correct
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What drug works by increasing the release of dopamine?
Your Answer: Amphetamine
Explanation:Amphetamine induces the direct release of dopamine by stimulating it, while also causing the internalization of dopamine transporters from the cell surface. In contrast, cocaine only blocks dopamine transporters and does not induce dopamine release.
Mechanisms of action for illicit drugs can be classified based on their effects on ionotropic receptors of ion channels, G coupled receptors, of monoamine transporters. Cocaine and amphetamine both increase dopamine levels in the synaptic cleft, but through different mechanisms. Cocaine directly blocks the dopamine transporter, while amphetamine binds to the transporter and increases dopamine efflux through various mechanisms, including inhibition of vesicular monoamine transporter 2 and monoamine oxidase, and stimulation of the intracellular receptor TAAR1. These mechanisms result in increased dopamine levels in the synaptic cleft and reuptake inhibition.
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This question is part of the following fields:
- Psychopharmacology
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Question 22
Correct
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Which of the following is not a way in which galantamine works?
Your Answer: Inhibits butyrylcholinesterase
Explanation:In the treatment of Alzheimer’s disease, acetylcholinesterase inhibitors such as galantamine are utilized to enhance central acetylcholine levels. Although they share this common mechanism of action, there are variations in how they function. Unlike galantamine, rivastigmine has the ability to inhibit butyrylcholinesterase.
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This question is part of the following fields:
- Psychopharmacology
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Question 23
Incorrect
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Which one of the following statements is accurate regarding psychiatric disorders in the elderly population?
Your Answer: The onset of puerperal psychosis is often in first two days
Correct Answer: Sulpiride should be avoided in breastfeeding mothers
Explanation:Puerperal psychosis does not have a specific set of symptoms, syndrome, of course, and about one in 500 live births are affected by it. During the episode of in recurrences, a bipolar pattern is often observed, and there is a higher incidence of puerperal attacks in women with manic-depressive rather than schizophrenic disorders. Suicide threats are common, but the risk of suicide is lower in parous mothers than in nulliparous women. Antipsychotics excreted in breast milk are unlikely to be harmful, but animal studies suggest potential adverse effects on the developing nervous system, and sulpiride should be avoided during breastfeeding. If standard psychotropic treatments fail, electroconvulsive therapy (ECT) may be considered, and it is particularly effective in postpartum psychosis. The onset of postpartum psychoses is usually rapid, occurring between two and 14 days after delivery, and almost any psychotic symptom may be present.
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This question is part of the following fields:
- Psychopharmacology
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Question 24
Incorrect
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A 45-year-old man with a mild depressive disorder currently taking an SSRI reports worsening tiredness. His blood test shows a sodium level of 122 mmol/L.
Which antidepressant would be more suitable in this situation?Your Answer: Mirtazapine
Correct Answer: Agomelatine
Explanation:Unlike other antidepressants, agomelatine (Valdoxan) does not affect serotonin transmission and is a melatonin agonist. It has a good safety profile and there have been no reported cases of hyponatraemia associated with its use. On the other hand, the other listed antidepressants have been linked to hyponatraemia.
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This question is part of the following fields:
- Psychopharmacology
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Question 25
Correct
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What type of antidepressant medication did Carlsson create in the late 1960s?
Your Answer: SSRI
Explanation:A Historical Note on the Development of Zimelidine, the First Selective Serotonin Reuptake Inhibitor
In 1960s, evidence began to emerge suggesting a significant role of serotonin in depression. This led to the development of zimelidine, the first selective serotonin reuptake inhibitor (SSRI). Zimelidine was derived from pheniramine and was marketed in Europe in 1982. However, it was removed from the market in 1983 due to severe side effects such as hypersensitivity reactions and Guillain-Barre syndrome.
Despite its short-lived availability, zimelidine paved the way for the development of other SSRIs such as fluoxetine, which was approved by the FDA in 1987 and launched in the US market in 1988 under the trade name Prozac. The development of SSRIs revolutionized the treatment of depression and other mood disorders, providing a safer and more effective alternative to earlier antidepressants such as the tricyclics and MAO inhibitors.
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This question is part of the following fields:
- Psychopharmacology
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Question 26
Correct
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What is the term used to describe an agonist that produces effects below the maximum level at a receptor?
Your Answer: A partial agonist
Explanation:Agonists and Antagonists in Pharmacology
In pharmacology, an agonist is a substance that binds to a receptor and triggers a biological response. On the other hand, an antagonist is a substance that blocks the effects of an agonist. A partial agonist produces a response but cannot produce the maximum response even at high doses.
Competitive antagonists bind to the receptor in a reversible way without affecting the biological response. They make the agonist appear less potent. Inverse agonists, on the other hand, have opposite effects from those of full agonists. They are not the same as antagonists, which block the effect of both agonists and inverse agonists.
Full agonists display full efficacy at a receptor. Some substances can act as an agonist at certain receptors and as an antagonist at others. Such a substance is called an agonist-antagonist. Understanding the differences between agonists and antagonists is crucial in drug development and treatment.
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This question is part of the following fields:
- Psychopharmacology
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Question 27
Correct
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What is a possible approach to enhance treatment for a patient with hyperprolactinaemia caused by risperidone?
Your Answer: Aripiprazole
Explanation:In certain cases, the addition of 5-10 mg of aripiprazole has demonstrated the ability to restore hyperprolactinaemia to normal levels.
Antipsychotics and Sexual Dysfunction: Causes, Risks, and Management
Sexual dysfunction is a common side effect of antipsychotic medication, with the highest risk associated with risperidone and haloperidol due to their effect on prolactin levels. Clozapine, olanzapine, quetiapine, aripiprazole, asenapine, and lurasidone are associated with lower rates of sexual dysfunction. The Arizona Sexual Experiences Scale (ASEX) can be used to measure sexual dysfunction before and during treatment. Management options include excluding other causes, watchful waiting, dose reduction, switching to a lower risk agent, adding aripiprazole, considering an antidote medication, of using sildenafil for erectile dysfunction. It is important to address sexual dysfunction to improve quality of life and medication adherence.
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This question is part of the following fields:
- Psychopharmacology
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Question 28
Correct
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For what purpose is Modafinil licensed?
Your Answer: Obstructive sleep apnoea
Explanation:Modafinil: A Psychostimulant for Wakefulness and Attention Enhancement
Modafinil is a type of psychostimulant that is known to improve wakefulness, attention, and vigilance. Although it is similar to amphetamines, it does not produce the same euphoric effects and is not associated with dependence of tolerance. Additionally, it does not seem to cause psychosis. Modafinil is approved for the treatment of narcolepsy, obstructive sleep apnea, and chronic shift work. It is also suggested as an adjunctive treatment for depression by the Maudsley. Recently, it has gained popularity as a smart drug due to its potential to enhance cognitive functioning in healthy individuals.
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This question is part of the following fields:
- Psychopharmacology
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Question 29
Correct
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A young adult who has just begun taking olanzapine reports experiencing dizziness, euphoria, and blurred vision upon sudden standing. What would be the most suitable replacement medication?
Your Answer: Amisulpride
Explanation:The patient’s reported symptoms are indicative of postural hypotension, which is likely a side effect of the olanzapine medication they were given.
Maudsley Guidelines: Antipsychotics for Postural Hypotension
When postural hypotension is a concern, it may be necessary to switch to an antipsychotic that is less likely to cause this side effect. The following antipsychotics are recommended by the Maudsley Guidelines:
– Amisulpride
– Aripiprazole
– Haloperidol
– Sulpiride
– TrifluoperazineThese medications have a lower risk of causing postural hypotension compared to other antipsychotics such as risperidone, clozapine, olanzapine, paliperidone, quetiapine, and ziprasidone. It is important to discuss any concerns about side effects with a healthcare provider before making any changes to medication.
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This question is part of the following fields:
- Psychopharmacology
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Question 30
Incorrect
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Which of the following antipsychotics is currently offered in the United Kingdom as a prolonged-release injection?
Your Answer: Amisulpride
Correct Answer: Olanzapine
Explanation:Olanzapine pamoate is the only antipsychotic with a long acting injectable (LAI) form. A three hour observation period is necessary after administration due to the potential for post-injection syndrome. The remaining antipsychotics do not have an LAI form available.
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This question is part of the following fields:
- Psychopharmacology
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Question 31
Correct
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What is the presumed cause of the sexual dysfunction associated with SSRIs?
Your Answer: 5-HT2 agonism
Explanation:The inhibition of sexual behavior is caused by the activation of 5-HT2 receptors. However, this effect can be reversed by using 5-HT2 antagonists like cyproheptadine and 5-HT1a agonists like buspirone. These drugs are effective in treating sexual dysfunction caused by selective serotonin reuptake inhibitors (SSRIs).
Antidepressants can cause sexual dysfunction as a side-effect, although the rates vary. The impact on sexual desire, arousal, and orgasm can differ depending on the type of antidepressant. It is important to rule out other causes and consider non-pharmacological strategies such as reducing the dosage of taking drug holidays. If necessary, switching to a lower risk antidepressant of using pharmacological options such as phosphodiesterase inhibitors of mirtazapine augmentation can be considered. The Maudsley Guidelines 14th Edition provides a helpful table outlining the risk of sexual dysfunction for different antidepressants.
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This question is part of the following fields:
- Psychopharmacology
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Question 32
Correct
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What is the definition of priapism?
Your Answer: A persistent and painful erection
Explanation:Priapism: A Painful and Persistent Erection
Priapism is a condition characterized by a prolonged and painful erection, which can occur in males and even in the clitoris. Although rare, certain medications such as antipsychotics and antidepressants have been known to cause priapism. The primary mechanism behind this condition is alpha blockade, although other mechanisms such as serotonin-mediated pathways have also been suggested. Some of the drugs most commonly associated with priapism include Trazodone, Chlorpromazine, and Thioridazine. Treatment involves the use of alpha-adrenergic agonists, which can be administered orally of injected directly into the penis. Priapism is a serious condition that can lead to complications such as penile amputation, although such cases are extremely rare.
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This question is part of the following fields:
- Psychopharmacology
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Question 33
Correct
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What is a known factor that can cause hypospadias when taken during pregnancy?
Your Answer: Valproic acid
Explanation:Teratogens and Their Associated Defects
Valproic acid is a teratogen that has been linked to various birth defects, including neural tube defects, hypospadias, cleft lip/palate, cardiovascular abnormalities, developmental delay, endocrinological disorders, limb defects, and autism (Alsdorf, 2005). Lithium has been associated with cardiac anomalies, specifically Ebstein’s anomaly. Alcohol consumption during pregnancy can lead to cleft lip/palate and fetal alcohol syndrome. Phenytoin has been linked to fingernail hypoplasia, craniofacial defects, limb defects, cerebrovascular defects, and mental retardation. Similarly, carbamazepine has been associated with fingernail hypoplasia and craniofacial defects. Diazepam has been linked to craniofacial defects, specifically cleft lip/palate (Palmieri, 2008). The evidence for steroids causing craniofacial defects is not convincing, according to the British National Formulary (BNF). Selective serotonin reuptake inhibitors (SSRIs) have been associated with congenital heart defects and persistent pulmonary hypertension (BNF). It is important for pregnant women to avoid exposure to these teratogens to reduce the risk of birth defects in their babies.
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This question is part of the following fields:
- Psychopharmacology
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Question 34
Correct
-
What factor is most likely to worsen a patient's psoriasis?
Your Answer: Lithium
Explanation:Lithium – Pharmacology
Pharmacokinetics:
Lithium salts are rapidly absorbed following oral administration and are almost exclusively excreted by the kidneys unchanged. Blood samples for lithium should be taken 12 hours post-dose.Ebstein’s:
Ebstein’s anomaly is a congenital malformation consisting of a prolapse of the tricuspid valve into the right ventricle. It occurs in 1:20,000 of the general population. Initial data suggested it was more common in those using lithium but this had not held to be true.Contraindications:
Addison’s disease, Brugada syndrome, cardiac disease associated with rhythm disorders, clinically significant renal impairment, untreated of untreatable hypothyroidism, low sodium levels.Side-effects:
Common side effects include nausea, tremor, polyuria/polydipsia, rash/dermatitis, blurred vision, dizziness, decreased appetite, drowsiness, metallic taste, and diarrhea. Side-effects are often dose-related.Long-term use is associated with hypothyroidism, hyperthyroidism, hypercalcemia/hyperparathyroidism, irreversible nephrogenic diabetes insipidus, and reduced GFR.
Lithium-induced diabetes insipidus:
Treatment options include stopping lithium (if feasible), keeping levels within 0.4-0.8 mmol/L, once-daily dose of the drug taken at bedtime, amiloride, thiazide diuretics, indomethacin, and desmopressin.Toxicity:
Lithium salts have a narrow therapeutic/toxic ratio. Risk factors for lithium toxicity include drugs altering renal function, decreased circulating volume, infections, fever, decreased oral intake of water, renal insufficiency, and nephrogenic diabetes insipidus. Features of lithium toxicity include GI symptoms and neuro symptoms.Pre-prescribing:
Before prescribing lithium, renal function, cardiac function, thyroid function, FBC, and BMI should be checked. Women of childbearing age should be advised regarding contraception, and information about toxicity should be provided.Monitoring:
Lithium blood levels should be checked weekly until stable, and then every 3-6 months once stable. Thyroid and renal function should be checked every 6 months. Patients should be issued with an information booklet, alert card, and record book. -
This question is part of the following fields:
- Psychopharmacology
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Question 35
Correct
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Which antipsychotic medication has the strongest binding affinity for D4 receptors?
Your Answer: Clozapine
Explanation:Mechanisms of Action of Different Drugs
Understanding the mechanisms of action of different drugs is crucial for medical professionals. It is a common topic in exams and can earn easy marks if studied well. This article provides a list of drugs and their mechanisms of action in different categories such as antidepressants, anti dementia drugs, mood stabilizers, anxiolytic/hypnotic drugs, antipsychotics, drugs of abuse, and other drugs. For example, mirtazapine is a noradrenaline and serotonin specific antidepressant that works as a 5HT2 antagonist, 5HT3 antagonist, H1 antagonist, alpha 1 and alpha 2 antagonist, and moderate muscarinic antagonist. Similarly, donepezil is a reversible acetylcholinesterase inhibitor used as an anti dementia drug, while valproate is a GABA agonist and NMDA antagonist used as a mood stabilizer. The article also explains the mechanisms of action of drugs such as ketamine, phencyclidine, buprenorphine, naloxone, atomoxetine, varenicline, disulfiram, acamprosate, and sildenafil.
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This question is part of the following fields:
- Psychopharmacology
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Question 36
Incorrect
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What is the truth about the discontinuation symptoms that are linked to antidepressants?
Your Answer: The onset of discontinuation symptoms is usually within 24 hours of stopping treatment
Correct Answer: Suicidal thoughts are associated with discontinuation of paroxetine
Explanation:Discontinuation symptoms are common when stopping most antidepressants, typically appearing within 5 days of treatment cessation. However, these symptoms are more likely to occur with short half-life drugs like paroxetine, especially when doses are missed. It’s important to note that discontinuing paroxetine may lead to suicidal thoughts, so patients should be informed of the potential risks associated with poor compliance.
Antidepressants can cause discontinuation symptoms when patients stop taking them, regardless of the type of antidepressant. These symptoms usually occur within 5 days of stopping the medication and can last up to 3 weeks. Symptoms include flu-like symptoms, dizziness, insomnia, vivid dreams, irritability, crying spells, and sensory symptoms. SSRIs and related drugs with short half-lives, such as paroxetine and venlafaxine, are particularly associated with discontinuation symptoms. Tapering antidepressants at the end of treatment is recommended to prevent these symptoms. TCAs and MAOIs are also associated with discontinuation symptoms, with amitriptyline and imipramine being the most common TCAs and all MAOIs being associated with prominent discontinuation symptoms. Patients at highest risk for discontinuation symptoms include those on antidepressants with shorter half-lives, those who have been taking antidepressants for 8 weeks of longer, those using higher doses, younger people, and those who have experienced discontinuation symptoms before. Agomelatine is not associated with any discontinuation syndrome. If a discontinuation reaction occurs, restarting the antidepressant of switching to an alternative with a longer half-life and tapering more slowly may be necessary. Explanation and reassurance are often sufficient for mild symptoms. These guidelines are based on the Maudsley Guidelines 14th Edition and a study by Tint (2008).
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This question is part of the following fields:
- Psychopharmacology
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Question 37
Correct
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Which drug interacts with an ionotropic receptor to produce its effects?
Your Answer: Benzodiazepines
Explanation:Mechanisms of action for illicit drugs can be classified based on their effects on ionotropic receptors of ion channels, G coupled receptors, of monoamine transporters. Cocaine and amphetamine both increase dopamine levels in the synaptic cleft, but through different mechanisms. Cocaine directly blocks the dopamine transporter, while amphetamine binds to the transporter and increases dopamine efflux through various mechanisms, including inhibition of vesicular monoamine transporter 2 and monoamine oxidase, and stimulation of the intracellular receptor TAAR1. These mechanisms result in increased dopamine levels in the synaptic cleft and reuptake inhibition.
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This question is part of the following fields:
- Psychopharmacology
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Question 38
Correct
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Which substances are metabolized by the enzyme CYP1A2?
Your Answer: Clozapine
Explanation:The Cytochrome P450 system is a group of enzymes that metabolize drugs by altering their functional groups. The system is located in the liver and small intestine and is involved in drug interactions through enzyme induction of inhibition. Notable inducers include smoking, alcohol, and St John’s Wort, while notable inhibitors include grapefruit juice and some SSRIs. CYP2D6 is important due to genetic polymorphism, and CYP3A4 is the most abundant subfamily and is commonly involved in interactions. Grapefruit juice inhibits both CYP1A2 and CYP3A4, while tobacco smoking induces CYP1A2. The table summarizes the main substrates, inhibitors, and inducers for each CYP enzyme.
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This question is part of the following fields:
- Psychopharmacology
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Question 39
Correct
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Which adverse drug reaction is correctly paired with its corresponding Gell and Coombs classification system?
Your Answer: Type II - cytotoxic
Explanation:Adverse Drug Reactions (ADRs) refer to the harmful effects associated with the use of a medication at a normal dose. These reactions are classified into two types: Type A and Type B. Type A reactions can be predicted from the pharmacology of the drug and are dose-dependent, meaning they can be reversed by withdrawing the drug. On the other hand, Type B reactions cannot be predicted from the known pharmacology of the drug and include allergic reactions.
Type A reactions account for up to 80% of all ADRs, while Type B reactions are less common. Allergic reactions are a type of Type B reaction and are further subdivided by Gell and Coombs into four types: Type I (IgE-mediated) reactions, Type II (cytotoxic) reactions, Type III (immune complex) reactions, and Type IV (cell-mediated) reactions. Proper identification and management of ADRs are crucial in ensuring patient safety and optimizing treatment outcomes.
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This question is part of the following fields:
- Psychopharmacology
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Question 40
Correct
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What medication does not impact the QTc interval?
Your Answer: Aripiprazole
Explanation:Aripiprazole does not affect the QTc interval and has minimal risk of extrapyramidal side effects, sedation, of weight gain. Amisulpride, citalopram, and quetiapine have a moderate effect on the QTc interval, which requires ECG monitoring due to a prolongation of >10 msec. Haloperidol has a high effect on the QTc interval, which mandates ECG monitoring due to a prolongation of >20 msec.
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This question is part of the following fields:
- Psychopharmacology
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Question 41
Correct
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What substance of drug directly inhibits the dopamine transporter, resulting in elevated levels of dopamine in the synaptic cleft?
Your Answer: Cocaine
Explanation:Amphetamine engages in competition with the DAT instead of obstructing it.
Mechanisms of action for illicit drugs can be classified based on their effects on ionotropic receptors of ion channels, G coupled receptors, of monoamine transporters. Cocaine and amphetamine both increase dopamine levels in the synaptic cleft, but through different mechanisms. Cocaine directly blocks the dopamine transporter, while amphetamine binds to the transporter and increases dopamine efflux through various mechanisms, including inhibition of vesicular monoamine transporter 2 and monoamine oxidase, and stimulation of the intracellular receptor TAAR1. These mechanisms result in increased dopamine levels in the synaptic cleft and reuptake inhibition.
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This question is part of the following fields:
- Psychopharmacology
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Question 42
Incorrect
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Can you provide an example of a drug interaction that affects the way a drug works in the body?
Your Answer: Enzyme inhibition
Correct Answer: Competition at a receptor
Explanation:Drug Interactions: Understanding the Different Types
Drug interactions can occur in different ways, and it is important to understand the different types to avoid potential harm. Pharmacokinetic drug interactions happen when one drug affects the metabolism, absorption, of excretion of another drug. This can be due to enzyme induction of inhibition, changes in gastrointestinal tract motility and pH, chelation, competition for renal tubular transport, of changes in protein binding. On the other hand, pharmacodynamic drug interactions occur when one drug directly alters the effect of another drug. This can happen through synergism, antagonism, of interaction at receptors, such as allosteric modulation. It is important to note that pharmacodynamic drug interactions do not involve any absorption, distribution, metabolism, of excretion processes directly. By understanding the different types of drug interactions, healthcare professionals can better manage patients’ medications and prevent potential adverse effects.
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This question is part of the following fields:
- Psychopharmacology
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Question 43
Correct
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Which medication is metabolized into nortriptyline as its active form?
Your Answer: Amitriptyline
Explanation:Antidepressants with Active Metabolites
Many antidepressants have active metabolites that can affect the body’s response to the medication. For example, amitriptyline has nortriptyline as an active metabolite, while clomipramine has desmethyl-clomipramine. Other antidepressants with active metabolites include dosulepin, doxepin, imipramine, lofepramine, fluoxetine, mirtazapine, trazodone, and venlafaxine.
These active metabolites can have different effects on the body compared to the original medication. For example, nortriptyline is a more potent inhibitor of serotonin and norepinephrine reuptake than amitriptyline. Similarly, desipramine, the active metabolite of imipramine and lofepramine, has a longer half-life and is less sedating than the original medication.
It is important for healthcare providers to be aware of the active metabolites of antidepressants when prescribing medication and monitoring patients for side effects and efficacy.
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This question is part of the following fields:
- Psychopharmacology
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Question 44
Correct
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Which of the following is linked to losing weight?
Your Answer: Topiramate
Explanation:Topiramate is a medication used for epilepsy and bipolar affective disorder. It works by inhibiting voltage gated sodium channels and increasing GABA levels. Unlike most psychotropic drugs, it is associated with weight loss.
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This question is part of the following fields:
- Psychopharmacology
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Question 45
Incorrect
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Which drug is most likely to cause porphyria to occur?
Your Answer: Chlorpromazine
Correct Answer: Diazepam
Explanation:Porphyria: The Little Imitator
Porphyria is a medical condition that is often referred to as the little imitator because it can mimic various common psychiatric presentations. This condition can be triggered by the use of certain psychotropic drugs, including barbiturates, benzodiazepines, sulpiride, and some mood stabilizers.
Porphyria can manifest in different ways, and it is important to be aware of the symptoms. These may include abdominal pain, mental state changes, constipation, vomiting, and muscle weakness.
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This question is part of the following fields:
- Psychopharmacology
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Question 46
Correct
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What is the correct definition of the QT interval?
Your Answer: The QT interval is measured from the beginning of the QRS complex to the end of the T wave
Explanation:QTc Prolongation: Risks and Identification
The QT interval is a measure of the time it takes for the ventricles to repolarize and is calculated from the beginning of the QRS complex to the end of the T wave. However, the QT interval varies with the heart rate, making it difficult to use a single number as a cut-off for a prolonged QT. Instead, a corrected QT interval (QTc) is calculated for each heart rate using various formulas. A QTc over the 99th percentile is considered abnormally prolonged, with approximate values of 470 ms for males and 480 ms for females.
Prolonged QT intervals can lead to torsade de pointes (TdP), a polymorphic ventricular tachycardia that can be fatal if it degenerates into ventricular fibrillation. TdP is characterized by a twisting of the QRS complexes around an isoelectric line and is often asymptomatic but can also be associated with syncope and death. An accurate diagnosis requires an ECG to be recorded during the event. It is important to note that an increase in the QT interval due to a new conduction block should not be considered indicative of acquired LQTS and risk for TdP.
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This question is part of the following fields:
- Psychopharmacology
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Question 47
Correct
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What factor increases the risk of developing neuroleptic malignant syndrome?
Your Answer: Having Parkinson's disease
Explanation:The use of dopaminergic drugs in individuals with Parkinson’s disease increases their susceptibility to NMS. NMS is more likely to develop when there is a modification in the dosage of dopaminergic and antipsychotic medications. While it is possible, NMS does not typically arise without the administration of dopamine-affecting drugs.
Serotonin Syndrome and Neuroleptic Malignant Syndrome are two conditions that can be difficult to differentiate. Serotonin Syndrome is caused by excess serotonergic activity in the CNS and is characterized by neuromuscular abnormalities, altered mental state, and autonomic dysfunction. On the other hand, Neuroleptic Malignant Syndrome is a rare acute disorder of thermoregulation and neuromotor control that is almost exclusively caused by antipsychotics. The symptoms of both syndromes can overlap, but there are some distinguishing clinical features. Hyper-reflexia, ocular clonus, and tremors are more prominent in Serotonin Syndrome, while Neuroleptic Malignant Syndrome is characterized by uniform ‘lead-pipe’ rigidity and hyporeflexia. Symptoms of Serotonin Syndrome usually resolve within a few days of stopping the medication, while Neuroleptic Malignant Syndrome can take up to 14 days to remit with appropriate treatment. The following table provides a useful guide to the main differentials of Serotonin Syndrome and Neuroleptic Malignant Syndrome.
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This question is part of the following fields:
- Psychopharmacology
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Question 48
Correct
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Which of the following is not considered a known factor that increases the risk of lithium toxicity?
Your Answer: Hepatic impairment
Explanation:Lithium – Pharmacology
Pharmacokinetics:
Lithium salts are rapidly absorbed following oral administration and are almost exclusively excreted by the kidneys unchanged. Blood samples for lithium should be taken 12 hours post-dose.Ebstein’s:
Ebstein’s anomaly is a congenital malformation consisting of a prolapse of the tricuspid valve into the right ventricle. It occurs in 1:20,000 of the general population. Initial data suggested it was more common in those using lithium but this had not held to be true.Contraindications:
Addison’s disease, Brugada syndrome, cardiac disease associated with rhythm disorders, clinically significant renal impairment, untreated of untreatable hypothyroidism, low sodium levels.Side-effects:
Common side effects include nausea, tremor, polyuria/polydipsia, rash/dermatitis, blurred vision, dizziness, decreased appetite, drowsiness, metallic taste, and diarrhea. Side-effects are often dose-related.Long-term use is associated with hypothyroidism, hyperthyroidism, hypercalcemia/hyperparathyroidism, irreversible nephrogenic diabetes insipidus, and reduced GFR.
Lithium-induced diabetes insipidus:
Treatment options include stopping lithium (if feasible), keeping levels within 0.4-0.8 mmol/L, once-daily dose of the drug taken at bedtime, amiloride, thiazide diuretics, indomethacin, and desmopressin.Toxicity:
Lithium salts have a narrow therapeutic/toxic ratio. Risk factors for lithium toxicity include drugs altering renal function, decreased circulating volume, infections, fever, decreased oral intake of water, renal insufficiency, and nephrogenic diabetes insipidus. Features of lithium toxicity include GI symptoms and neuro symptoms.Pre-prescribing:
Before prescribing lithium, renal function, cardiac function, thyroid function, FBC, and BMI should be checked. Women of childbearing age should be advised regarding contraception, and information about toxicity should be provided.Monitoring:
Lithium blood levels should be checked weekly until stable, and then every 3-6 months once stable. Thyroid and renal function should be checked every 6 months. Patients should be issued with an information booklet, alert card, and record book. -
This question is part of the following fields:
- Psychopharmacology
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Question 49
Correct
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Which of the following medications has a chemical composition that closely resembles diazepam?
Your Answer: Chlordiazepoxide
Explanation:Chlordiazepoxide belongs to the benzodiazepine class of drugs and shares a similar chemical structure with diazepam.
Clomethiazole is a type of hypnotic that is not classified as a benzodiazepine.
Chloroquine is primarily used as an antimalarial medication.
Chlorphenamine is an antihistamine drug.
Chlorpromazine is classified as a typical antipsychotic medication. -
This question is part of the following fields:
- Psychopharmacology
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Question 50
Correct
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What physiological factor is the QTc, calculated using Bazett's formula, corrected for?
Your Answer: RR interval
Explanation:The Bazett formula adjusts the QT interval for heart rate by taking the square root of the R-R interval and dividing the QT interval by it.
QTc Prolongation: Risks and Identification
The QT interval is a measure of the time it takes for the ventricles to repolarize and is calculated from the beginning of the QRS complex to the end of the T wave. However, the QT interval varies with the heart rate, making it difficult to use a single number as a cut-off for a prolonged QT. Instead, a corrected QT interval (QTc) is calculated for each heart rate using various formulas. A QTc over the 99th percentile is considered abnormally prolonged, with approximate values of 470 ms for males and 480 ms for females.
Prolonged QT intervals can lead to torsade de pointes (TdP), a polymorphic ventricular tachycardia that can be fatal if it degenerates into ventricular fibrillation. TdP is characterized by a twisting of the QRS complexes around an isoelectric line and is often asymptomatic but can also be associated with syncope and death. An accurate diagnosis requires an ECG to be recorded during the event. It is important to note that an increase in the QT interval due to a new conduction block should not be considered indicative of acquired LQTS and risk for TdP.
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This question is part of the following fields:
- Psychopharmacology
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Question 51
Correct
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Which drug has a very small margin of safety between its therapeutic and toxic doses?
Your Answer: Lithium
Explanation:Due to its low therapeutic index, lithium necessitates monitoring.
Narrow Therapeutic Index Drugs
Narrow therapeutic index (NTI) drugs are medications that have a small difference between the amount that causes a therapeutic effect and the amount that causes toxicity. In other words, the therapeutic index (TI) of these drugs is narrow. The TI is a ratio that compares the blood concentration at which a drug causes a therapeutic effect to the amount that causes death of toxicity.
In clinical practice, the TI is the range of doses at which a medication appeared to be effective in clinical trials for a median of participants without unacceptable adverse effects. For most drugs, this range is wide enough, and the maximum plasma concentration of the drug achieved when the recommended doses of a drug are prescribed lie sufficiently above the minimum therapeutic concentration and sufficiently below the toxic concentration.
However, some drugs have a narrow therapeutic index, which means that even small changes in dose of blood concentration can lead to serious adverse effects. The US Food and Drug Administration (FDA) defines a drug product as having an NTI when there is less than a twofold difference in the minimum toxic concentrations and minimum effective concentrations in the blood and safe and effective use of the drug requires careful titration and patient monitoring.
Examples of drugs with a narrow therapeutic index include carbamazepine, lithium, phenytoin, warfarin, digoxin, and gentamicin. These drugs require close monitoring to ensure that the blood concentration remains within the therapeutic range and does not reach toxic levels.
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This question is part of the following fields:
- Psychopharmacology
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Question 52
Correct
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What is a true statement about varenicline?
Your Answer: It is recommended by NICE for smoking cessation
Explanation:Champix is a medication that contains varenicline, which acts as a partial agonist at nicotinic receptors.
Varenicline for Smoking Cessation: Safety and Efficacy
Varenicline is a medication used to aid smoking cessation by reducing cravings and pleasurable effects of tobacco products. It has a high affinity for the alpha 4 beta 2 nicotinic receptor and is recommended by NICE for smoking cessation. Varenicline is safe to use in cases of liver dysfunction as it undergoes very little hepatic metabolism. It has been found to be nearly 80% more effective than bupropion and more effective than 24-hour nicotine replacement therapy in two large randomized controlled trials. The initial course of treatment could last 12 weeks, with an additional 12 weeks offered to those who have successfully quit smoking. However, varenicline has been observed to exacerbate underlying psychiatric illness, including depression, and is associated with changes in behavior of thinking, anxiety, psychosis, mood swings, aggressive behavior, suicidal ideation, and behavior. Patients with a psychiatric history should be closely monitored while taking varenicline. One randomized controlled trial has challenged this concern. The FDA has issued a safety announcement that varenicline may be associated with a small, increased risk of certain cardiovascular adverse events in patients with cardiovascular disease. The very common side effects of varenicline include nasopharyngitis, abnormal dreams, insomnia, headache, and nausea.
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This question is part of the following fields:
- Psychopharmacology
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Question 53
Incorrect
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What is the definition of latency period in pharmacology, and how does it related to the time between drug absorption and the onset of a specific pharmacologic effect?
Your Answer: Volume of distribution
Correct Answer: First pass effect
Explanation:The First Pass Effect in Psychiatric Drugs
The first-pass effect is a process in drug metabolism that significantly reduces the concentration of a drug before it reaches the systemic circulation. This phenomenon is related to the liver and gut wall, which absorb and metabolize the drug before it can enter the bloodstream. Psychiatric drugs are not exempt from this effect, and some undergo a significant reduction in concentration before reaching their target site. Examples of psychiatric drugs that undergo a significant first-pass effect include imipramine, fluphenazine, morphine, diazepam, and buprenorphine. On the other hand, some drugs undergo little to no first-pass effect, such as lithium and pregabalin.
Orally administered drugs are the most affected by the first-pass effect. However, there are other routes of administration that can avoid of partly avoid this effect. These include sublingual, rectal (partly avoids first pass), intravenous, intramuscular, transdermal, and inhalation. Understanding the first-pass effect is crucial in drug development and administration, especially in psychiatric drugs, where the concentration of the drug can significantly affect its efficacy and safety.
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This question is part of the following fields:
- Psychopharmacology
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Question 54
Correct
-
What is a known risk factor for QT prolongation when analyzing an ECG?
Your Answer: Hypokalemia
Explanation:Amantadine and QTc Prolongation
Amantadine is a medication used to treat Parkinson’s disease and influenza. It has been associated with QTc prolongation, which can increase the risk of Torsades de points. Therefore, caution should be exercised when prescribing amantadine to patients with risk factors for QT prolongation. If a patient is already taking amantadine and develops a prolonged QTc interval, the medication should be discontinued and an alternative treatment considered. It is important to monitor the QTc interval in patients taking amantadine, especially those with risk factors for QT prolongation.
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This question is part of the following fields:
- Psychopharmacology
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Question 55
Correct
-
The most probable diagnosis for a diabetic patient who has started taking antidepressants and presents with symptoms of nausea, headaches, and low plasma sodium levels is:
Your Answer: SIADH
Explanation:Hyponatremia in Psychiatric Patients
Hyponatremia, of low serum sodium, can occur in psychiatric patients due to the disorder itself, its treatment, of other medical conditions. Symptoms include nausea, confusion, seizures, and muscular cramps. Drug-induced hyponatremia is known as the syndrome of inappropriate antidiuretic hormone hypersecretion (SIADH), which results from excessive secretion of ADH and fluid overload. Diagnosis is based on clinically euvolaemic state with low serum sodium and osmolality, raised urine sodium and osmolality. SSRIs, SNRIs, and tricyclics are the most common drugs that can cause SIADH. Risk factors for SIADH include starting a new drug, and treatment usually involves fluid restriction and sometimes demeclocycline.
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This question is part of the following fields:
- Psychopharmacology
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Question 56
Incorrect
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Which statement accurately describes the CATIE study?
Your Answer: It is the largest pragmatic trial conducted in the UK
Correct Answer: Olanzapine was found to be more effective than the other atypical antipsychotics used in phase I
Explanation:Olanzapine was found to have the highest duration of treatment before discontinuation due to inadequate efficacy, the longest period of successful treatment, and the lowest number of hospitalizations caused by worsening of schizophrenia among the patients.
CATIE Study: Comparing Antipsychotic Medications for Schizophrenia Treatment
The Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) Study, funded by the National Institute of Mental Health (NIMH), was a nationwide clinical trial that aimed to compare the effectiveness of older and newer antipsychotic medications used to treat schizophrenia. It is the largest, longest, and most comprehensive independent trial ever conducted to examine existing therapies for schizophrenia. The study consisted of two phases.
Phase I of CATIE compared four newer antipsychotic medications to one another and an older medication. Participants were followed for 18 months to evaluate longer-term patient outcomes. The study involved over 1400 participants and was conducted at various treatment sites, representative of real-life settings where patients receive care. The results from CATIE are applicable to a wide range of people with schizophrenia in the United States.
The medications were comparably effective, but high rates of discontinuation were observed due to intolerable side-effects of failure to adequately control symptoms. Olanzapine was slightly better than the other drugs but was associated with significant weight gain as a side-effect. Surprisingly, the older, less expensive medication (perphenazine) used in the study generally performed as well as the four newer medications. Movement side effects primarily associated with the older medications were not seen more frequently with perphenazine than with the newer drugs.
Phase II of CATIE sought to provide guidance on which antipsychotic to try next if the first failed due to ineffectiveness of intolerability. Participants who discontinued their first antipsychotic medication because of inadequate management of symptoms were encouraged to enter the efficacy (clozapine) pathway, while those who discontinued their first treatment because of intolerable side effects were encouraged to enter the tolerability (ziprasidone) pathway. Clozapine was remarkably effective and was substantially better than all the other atypical medications.
The CATIE study also looked at the risk of metabolic syndrome (MS) using the US National Cholesterol Education Program Adult Treatment Panel criteria. The prevalence of MS at baseline in the CATIE group was 40.9%, with female patients being three times as likely to have MS compared to matched controls and male patients being twice as likely.
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This question is part of the following fields:
- Psychopharmacology
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Question 57
Correct
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Which antihistamine should be avoided when a patient is taking an MAOI medication?
Your Answer: Chlorpheniramine
Explanation:According to Gillman (1998), it is recommended to avoid using the antihistamines brompheniramine and chlorpheniramine as they act as serotonin reuptake inhibitors (SRIs). However, all other antihistamines are considered safe for use. Gillman’s study focused on the history and risk of serotonin syndrome.
MAOIs: A Guide to Mechanism of Action, Adverse Effects, and Dietary Restrictions
First introduced in the 1950s, MAOIs were the first antidepressants introduced. However, they are not the first choice in treating mental health disorders due to several dietary restrictions and safety concerns. They are only a treatment option when all other medications are unsuccessful. MAOIs may be particularly useful in atypical depression (over eating / over sleeping, mood reactivity).
MAOIs block the monoamine oxidase enzyme, which breaks down different types of neurotransmitters from the brain: norepinephrine, serotonin, dopamine, as well as tyramine. There are two types of monoamine oxidase, A and B. The MOA A are mostly distributed in the placenta, gut, and liver, but MOA B is present in the brain, liver, and platelets. Selegiline and rasagiline are irreversible and selective inhibitors of MAO type B, but safinamide is a reversible and selective MAO B inhibitor.
The most common adverse effects of MAOIs occurring early in treatment are orthostatic hypotension, daytime sleepiness, insomnia, and nausea; later common effects include weight gain, muscle pain, myoclonus, paraesthesia, and sexual dysfunction.
Pharmacodynamic interactions with MAOIs can cause two types of problem: serotonin syndrome (mainly due to SSRIs) and elevated blood pressure (caused by indirectly acting sympathomimetic amines releasers, like pseudoephedrine and phenylephrine). The combination of MAOIs and some TCAs appears safe. Only those TCAs with significant serotonin reuptake inhibition (clomipramine and imipramine) are likely to increase the risk of serotonin syndrome.
Tyramine is a monoamine found in various foods, and is an indirect sympathomimetic that can cause a hypertensive reaction in patients receiving MAOI therapy. For this reason, dietary restrictions are required for patients receiving MAOIs. These restrictions include avoiding matured/aged cheese, fermented sausage, improperly stored meat, fava of broad bean pods, and certain drinks such as on-tap beer. Allowed foods include fresh cottage cheese, processed cheese slices, fresh packaged of processed meat, and other alcohol (no more than two bottled or canned beers of two standard glasses of wine, per day).
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This question is part of the following fields:
- Psychopharmacology
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Question 58
Correct
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What is a side effect of sildenafil that occurs frequently, affecting more than 10% of users?
Your Answer: Headache
Explanation:Side effects of sildenafil (viagra) that occur frequently (affecting more than 1 in 10 people) include:
Antidepressants can cause sexual dysfunction as a side-effect, although the rates vary. The impact on sexual desire, arousal, and orgasm can differ depending on the type of antidepressant. It is important to rule out other causes and consider non-pharmacological strategies such as reducing the dosage of taking drug holidays. If necessary, switching to a lower risk antidepressant of using pharmacological options such as phosphodiesterase inhibitors of mirtazapine augmentation can be considered. The Maudsley Guidelines 14th Edition provides a helpful table outlining the risk of sexual dysfunction for different antidepressants.
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This question is part of the following fields:
- Psychopharmacology
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Question 59
Correct
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A 42-year-old female with a history of bipolar disorder is undergoing second line mood stabilisation therapy due to inadequate response to first line agents. She was discovered unconscious on the street. She has no history of seizures of fainting. All laboratory tests are normal except for a serum sodium level of 105 mmol/L (135-150). What is the most probable cause of this?
Your Answer: Carbamazepine
Explanation:Monitoring for hyponatraemia is essential when administering carbamazepine due to its established side effect. However, it is important to note that NICE recommends lithium, olanzapine, and valproate as first line agents for treating bipolar disorder, with carbamazepine being a second line option.
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This question is part of the following fields:
- Psychopharmacology
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Question 60
Correct
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How does bupropion work?
Your Answer: NDRI (noradrenaline dopamine reuptake inhibitor)
Explanation:Bupropion is classified as a noradrenaline dopamine reuptake inhibitor (NDRI) and functions by elevating the levels of neurotransmitters such as noradrenaline and dopamine. It has been utilized as an antidepressant and a smoking cessation aid.
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This question is part of the following fields:
- Psychopharmacology
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