Pharmacie Clinique Prof. Vireak Part 2

The requirement for clinical pharmacy is the following. Which is the most appropriate answer?
Knowledge of drug therapy
Knowledge of pharmacology
Knowledge of pharmacokinetic
All of the above
For the level of action of clinical pharmacy like before the prescription, which is best answer?
Clinical monitoring
Clinical trial
Counseling
None of the above
The principle activities of clinical pharmacist is:
Counseling
Selection of drugs
Drug information
All of the above
An 87-year-old woman has been taking digoxin for atrial fibrillation for 15 years, but now complains of nausea and reduced mobility. Her current dose of digoxin is 187.5 micrograms orally daily. Her digoxin level is 3.0 nmol/L (therapeutic range 1.0-2.6 nmol/L).Which of the following is the most appropriate course of action?
Continue the current dose
Prescribe digoxin-specific antibody fragments
Reduce the dose
Stop the digoxin and restart at a lower dose one the level is therapeutic
You are asked to compare the cost of four different antibacterial medicines. Which of the following treatment courses is the lowest cost?
Medicine A costs 17 USD for 28 tablets. The adult dose is one tablet twice a day and the usual treatment duration is 7 days.
Medicine B costs 30 USD for 100 tablets. The adult dose is one tablet four times a day and the usual treatment duration is 7 days.
Medicine C costs 20 USD for 25 tablets. The adult dose is one tablet twice a day and the usual treatment duration is 5 days
Medicine D costs 25 USD for 14 tablets. The adult dose is one tablet each day and the usual treatment duration is 5 days.
You are asked to compare the cost of four different anti-inflammatory skin preparations. Compare the cost of a day's treatment for each of the following preparations and determine which is the lowest cost?
Cream M costs 12 USD for a 30g tube. It is applied once or twice a day and one tube normally lasts two weeks.
Cream N costs 30 USD for a 100g tube. It is applied once or twice a day and one tube normally lasts 42 days.
Ointment P costs 20 USD for a 50g tube. It is applied once or twice a day and one tube normally lasts 50 days.
Gel O costs 25 USD for a 90g tube. It is applied once or twice a day and one tube normally lasts three months (84 days)
Mrs Baker was prescribed medicine X at a dose of 20mg three times a day for the first time last month. The usual dosage range is 30mg to 120mg daily. She tells you that her symptoms are not well controlled. She is not taking any other medication. Her prescriber asks your advice. What would you recommend?
Change the formulation to 60mg MR which she only needs to take once a day.
Use Therapeutic Drug Monitoring (TDM) to determine the actual level of drug in her blood.
Increase her dose so she is now taking 30mg three times a day.
Determine whether the patient has any difficulties taking the medicine
Which of the following patients are most at risk of suffering from an adverse drug reaction?
An 8-month year old infant receiving a prescription for an antibiotic.
A 22-year-old patient with asthma receiving prescriptions for inhalers to relieve and prevent their asthma.
A 48-year-old patient who has hypertension and receives a prescription for an ACE inhibitor.
A 68-year-old patient who has edema receiving a prescription for a diuretic
A 24-year-old woman has had a pulmonary embolism 4 week after giving birth. She has been prescribed warfarin. Her last INR (measured 1 week ago) was 1.7 (taking 5 mg of warfarin), so she was prescribed 7 mg, and has had her INR rechecked. Her current INR is 2.8.Which of the following is now the most appropriate dose?
5 mg
6 mg
7 mg
8 mg
We need to do therapeutic drug monitoring (TDM) because:
Narrow therapeutic index and high toxicity
Variation of plasma drug concentration
The effect is not measurable
All of the above
What does ICH stand for?
International convention on homogenization
International conference on harmonization
International conference on homogenization
International convention on harmonization
A Serious Adverse Event (SAE) is any untoward medical occurrence that at any dose:
Is life threatening
Requires inpatient hospitalization or prolongation of existing hospitalization
Results in persistent or significant disability/incapacity
All the above
What is the adverse drug reaction?
An undesirable event experienced by a patient whilst taking a medicine, regardless of whether or not the medicine is suspected to be related to the event.
The reaction may be a known side effect of the drug or it may be new and previously unrecognized.
A noxious and unintended response to a medicine that occurs at normal therapeutic doses used in humans for prophylaxis, diagnosis, or therapy of disease, or for the modificatio of physiologic function
All the above
A patient has an anaphylactic reaction after taking medication containing penicillin, what is the appropriate answer?
Type A reaction
Type B reaction
Type C reaction
Type D reaction
Mr. Ben takes warfarin 5 mg at every evening, actually he is bleeding. What is the appropriate answer?
Type A reaction
Type B reaction
Type C reaction
Type D reaction
A side effect or complication from a medication is:
Drug overdose
Late effect
Transition point
Adverse drug event
A patient has a second cancer after using alkylating agents for the treatment of Hodgkin’s disease, this is:
Type A reaction
Type B reaction
Type D reaction
Type E reaction
A patient has adrenocortical insufficiency after he stops a treatment with prednisolone. This is:
Type A reaction
Type B reaction
Type D reaction
Type E reaction
Side effect is:
A noxious and unintended response to a medicine that occurs at normal therapeutic doses used in humans for prophylaxis, diagnosis, or therapy of disease, or for the modification of physiologic function
Any untoward medical occurrence that may be present during treatment with a medicine but does not necessarily have a causal relationship with this treatment. ADE include medication errors and overdoses.
Any unintended effect of a pharmaceutical product occurring at normal therapeutic doses and is related to its pharmacological properties. Such effects may be well-known and even expected and require little or no change in patient management
All the above
Adverse drug reaction is classified in:
1
3
5
7
Iatrogenic Crushing's syndrome with prednisolone is:
Type B reaction
Type C reaction
Type D reaction
Type E reaction
Type A reaction is defined as:
Adverse effect that are known to occur from the pharmacology of the drug and are dose-related
Adverse effect that occur unpredictably and often have a high rate of morbidity and mortality.
Adverse effect that only occur during prolonged treatment and not with single doses
Adverse effect that occur when the drug is stopped, especially when it is stopped suddenly.
Type B reaction is defined as:
Adverse effect that are known to occur from the pharmacology of the drug and are dose-related.
Adverse effect that occur unpredictably and often have a high rate of morbidity and mortality
Adverse effect that only occur during prolonged treatment and not with single doses
Adverse effect that occur when the drug is stopped, especially when it is stopped suddenly.
Type C reaction is defined as:
Adverse effect that are known to occur from the pharmacology of the drug and are dose-related.
Adverse effect that occur unpredictably and often have a high rate of morbidity and mortality
Adverse effect that only occur during prolonged treatment and not with single doses
Adverse effect that occur when the drug is stopped, especially when it is stopped suddenly.
Type D reaction is defined as:
Adverse effect that are known to occur from the pharmacology of the drug and are dose-related.
Adverse effect that occur unpredictably and often have a high rate of morbidity and mortality.
Adverse effect that occur remote from treatment, either in the children of treated patients, or in patients themselves year after treatment
Adverse effect that occur when the drug is stopped, especially when it is stopped suddenly.
Type E reaction is defined as:
Adverse effect that are known to occur from the pharmacology of the drug and are dose-related.
Adverse effect that occur unpredictably and often have a high rate of morbidity and mortality.
Adverse effect that only occur during prolonged treatment and not with single doses
Adverse effect that occur when the drug is stopped, especially when it is stopped suddenly
Concerning drug interaction, which is the appropriate answer:
Drug interaction is the modification of the action of one drug by another
There are three kinds of mechanism of drug interaction
Drug interaction can result from one or combination of their three kinds of mechanism
All the above
The mechanism of drug interaction is/are:
Pharmacokinetic
Pharmaceutical
Pharmacodynamic
All the above
There is different type of drug interaction, which is/are the best answer:
Useful interaction
Drug-patient interaction
Drug-food interaction
All the above
Concerning drug interaction, using Angiotensin Converting Enzyme Inhibitor and thiazide diuretic in a patient with a hypertension is:
Increased effect
Minimizing side effect
Block acutely an unwanted effect
None of the above
Levodopa is used with dopa decarboxylase inhibitor in order to:
Increasing effect
Minimizing side effect
Block acutely an unwanted effect
All the above
A patient use gentamicin together with hydrocortisone, the mechanism of this drug interaction is:
Pharmaceutical interaction
Pharmacokinetic interaction
Pharmacodynamic interaction
Biological interaction
A patient use warfarin together with aspirin, the mechanism of this drug interaction is:
Pharmaceutical interaction
Pharmacokinetic interaction
Pharmacodynamic interaction
Biological interaction
A patient use lithium together with diuretic, the mechanism of this drug interaction is:
Pharmaceutical interaction
Pharmacokinetic interaction
Pharmacodynamic interaction
Biological interaction
Which is the level of interaction between warfarin and metronidazole?
Absorption
Metabolism
Distribution
Excretion
Which is the level of interaction between penicillin and probenecid?
Absorption
Metabolism
Distribution
Excretion
Pharmacodynamic interaction:
Occur outside the body
Interaction between drug with a similar effect
Occur when one drug influences the way in which another is handle by the body
All the above
Medication errors are the most frequently source of preventable medical errors in a hospital. Which of the following is not preventable?
Selecting a drug that the patient is allergic to without knowing of the allergy
Selecting the wrong dose
Selecting the wrong duration
Overlooking drug-drug interactions
The medication use process steps are:
Diagnosing, prescribing, preparing, dispensing, administering and monitoring tasks performed in different departments by different people
Diagnosing, prescribing, preparing, dispensing, administering, billing and monitoring tasks performed in different departments by different people
Diagnosing, prescribing, dispensing, preparing, administering and monitoring tasks performed in different departments by different people
Documenting, prescribing, preparing, dispensing, administering and monitoring tasks performed in different departments by different people
The most common causes of medication errors are lack of knowledge about the drug and:
Lack of information about the patient
Lack of timely test results
Lack of communication between EHRs
Lack of time spent reviewing the case
Which is the following agent is preferred in the treatment of insomnia?
Barbiturate
Ethanol
Phenothiazide
Benzodiazepine
Which statement about the process of drug discovery is true?
It only encompasses the non-clinical laboratory and animal testing.
It is the process which ascertains the effectiveness and safety of potential drug candidates
It is the process by which therapeutic compounds are formulated into medicines
It ensures there are no side-effects associated with the potential drug candidates
What are adverse drug reactions (ADRs)?
The synergistic effects that are seen when some drugs are administered concurrently
Responses to increased drug doses required to achieve the same physiological outcome
Unintended alternative physiological responses caused by the drug that cause harm to the patient
Harmful chemical interactions between two drugs that are used to treat the same clinical symptoms
In pharmacokinetics what does the acronym ADME stand for?
Absorption, Distribution, Metabolism, and Excretion
Administration, Differentiation, Metabolism, and Excretion
Absorption, Disintegration, Metabolism, and Efficacy
Administration, Distribution, Metabolism, and Efficacy
Which of the following is the correct definition of bioavailability?
Bioavailability describes the proportion of the drug administered that is metabolized very quickly and thus is not available to induce a physiological effect.
Bioavailability describes the ability of the administered drug metabolites to cause undesirable physiological effects
Bioavailability is used to describe the fraction of the dose of drug administered that is present within the body and facilitates the desired physiological effects
Bioavailability is the length of time an administered drug is present in the body and thus is available to cause a physiological effec
The role of health professional:
Identifying and assessing ADRs in clinical practice
Preventing ADRs
Monitoring therapy
All of the above
In the classification of immunological reaction, hemolytic anemia is in:
Type I
Type II
Type III
Type IV
The factor affecting susceptibility to ADR:
Age
Co-morbidity and concomitant medicine use
Ethnicity
All of the above
Among the drugs with high risk of interaction, ciclosporin is:
Concentration-dependent toxicity
Steep dose-response curve
Patient dependent on therapeutic effect
Saturable hepatic metabolism
Among the drugs with high risk of interaction, L-dopa is:
Concentration-dependent toxicity
Steep dose-response curve
Patient dependent on therapeutic effect
Saturable hepatic metabolism
Among the drugs with high risk of interaction, Cisplatin is:
Concentration-dependent toxicity
Steep dose-response curve
Patient dependent on therapeutic effect
Saturable hepatic metabolism
Among the drugs with high risk of interaction, Digoxin is:
Concentration-dependent toxicity
Steep dose-response curve
Patient dependent on therapeutic effect
Saturable hepatic metabolism
Among the drugs with high risk of interaction, Valproic acid is:
Concentration-dependent toxicity
Steep dose-response curve
Patient dependent on therapeutic effect
Saturable hepatic metabolism
Among the drugs with high risk of interaction, Valproic acid is:
Concentration-dependent toxicity
Steep dose-response curve
Patient dependent on therapeutic effect
Saturable hepatic metabolism
An 88-year-old woman is treated with Nisis® 80 mg 1 tab / day and Lovenox® 4000 anti Xa units / day. The patient’s renal function is considered to be normal (clearance of creatinine between 70 and 100 ml / min). The potassium level in the blood is 5.8 mmol/L. What is the intervention for this patient?
Drug substitution
Addition more drug
Stop using the drug
Therapeutic monitoring
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