Pharmacie clinique Pf.vireak ( 79-115)
79) 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 dosesand 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
81) Iatrogenic Crushing’s syndrome with prednisolone is:
Type B reaction
Type C reaction
Type D reaction
Type E reaction
82) 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.
83) 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.
84) 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.
85) 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.
86) 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
87) 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
88) The mechanism of drug interaction is/are:
Pharmacokinetic
Pharmaceutical
Pharmacodynamic
All the above
89) There is different type of drug interaction, which is/are the best answer:
Useful interaction
Drug-patient interaction
Drug-food interaction
All the above
90) 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
91) Levodopa is used with dopa decarboxylase inhibitor in order to:
Minimizing side effect
Increasing effect
Block acutely an unwanted effect
All the above
92) A patient use gentamicin together with hydrocortisone, the mechanism of this drug interaction is:
Pharmaceutical interaction
Pharmacokinetic interaction
Pharmacodynamic interaction
Biological interaction
93) A patient use warfarin together with aspirin, the mechanism of this drug interaction is:
Pharmaceutical interaction
Pharmacokinetic interaction
Biological interaction
Pharmacodynamic interaction
94) A patient use lithium together with diuretic, the mechanism of this drug interaction is:
Pharmacodynamic interaction
Pharmacokinetic interaction
Biological interaction
Pharmaceutical interaction
95) Which is the level of interaction between warfarin and metronidazole?
Absorption
Metabolism
Distribution
Excretion
96) Which is the level of interaction between penicillin and probenecid?
Absorption
Metabolism
Distribution
Excretion
97) 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
98) 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
99) 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
100) 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 time spent reviewing the case
Lack of communication between EHRs
101) Which is the following agent is preferred in the treatment of insomnia?
Barbiturate
Ethanol
Phenothiazide
Benzodiazepine
102) 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
103) 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
104) In pharmacokinetics what does the acronym ADME stand for?
Absorption, Distribution, Metabolism, and Excretion
Excretion Administration, Differentiation, Metabolism, and Excretion
Absorption, Disintegration, Metabolism, and Efficacy
Administration, Distribution, Metabolism, and Efficacy
105) 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 is used to describe the fraction of the dose of drug administered that is
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 effect
106) The role of health professional:
Identifying and assessing ADRs in clinical practice
Preventing ADRs
Monitoring therapy
All of the above
107) In the classification of immunological reaction, hemolytic anemia is in :
Type I
Type II
Type III
Type IV
108) The factor affecting susceptibility to ADR:
Age
Co-morbidity and concomitant medicine use
Ethnicity
All of the above
109) 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
110) 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
111) 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
112) 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
113) 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
114) 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
115) 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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