Module 4 Pharmacology - Pharmacokinetics - Toxicology Flashcards
(100 cards)
The ECG of the patient with Digoxin as his treatment in the therapeutic dose range would likely
to show:
A. Widening of the QRS complex
B. Elevation of the ST segment
C. Prolongation of the QT interval
D. Prolongation of the PR interval
Prolongation of the PR interval
The major segment of the nephron where the diuretic action of the thiazides took place
A. Cortical collecting tubule
B. Medullary collecting tubule
C. Distal convoluted tubule
D. Proximal convulated tubule
Distal convoluted tubule
The following statement/s are true for the Carbonic anhydrase inhibitors:
I. Depresses HCO3- reabsorption in the cortical collecting tubule.
II. Depresses HCO3- reabsorption in the proximal convoluted tubule.
III. Causes significant hyperchloremic metabolic acidosis
A. I only
B. II only
C. I and II only
D. II and III only
E. I,II and III
II and III only
What segments of nephron where the diuretic action of Spironolactone took place?
A. Cortical collecting tubule
B. Thick ascending limb of Henle’s
loop.
C. Thin ascending limb of Henle’s
loop.
D. Medullary collecting duct
Cortical collecting tubule
The activity of propranolol in the treatment of angina pectoris is the result of this mechanism
A. Decreased requirement for myocardial oxygen
B. Increased sensitivity to catecholamines
C. Reduced production of catecholamines
D. Dilation of the coronary vasculature
Decreased requirement for myocardial oxygen
A 56 year old male patient, with hypertension and DM type 2. He managed his diabetes by
insulin. What antihypertensive drug should not be used on his case?
A. Captopril
B. Propranolol
C. Methyldopa
D. Hydralazine
Propranolol
A drug given intravenously results in an AUC of 600 ug/mL-hr. If the same dose of drug is given
orally and the resulting AUC is 300 ug/mL-hr, what percentage of the oral dose reaches the
bloodstream?
A. 50 %
B. 30 %
C. 20 %
D. 60 %
E. 100 %
50 %
The time required to reach the minimum effective drug concentration in the blood is known as:
A. Duration of action
B. Frequency
C. Onset of action
D. Half-life
E. Intensity of action
Onset of action
The phenomenon where a drug could exist in more than one crystal form
A. Thixothrophy
B. Complexation
C. Polymorphism
D. Amorphism
E. Solvate formation
Polymorphism
The following statement/s are true for Potassium-sparing diuretics:
I. Inhibition of Na+ influx through ion channels in the luminal membrane
II. Inhibition by direct pharmacologic antagonism of mineralocorticoid receptors.
III. Renal K+ wasting may occur
A. I only
B. II only
C. I and II only
D. II and III only
E. I,II and III
I,II and III
The following statement/s are true for Quinidine.
I. Prolongs the QRS duration
II. Induction of torsade de pointes arrhythmia
III. Shortens the action potential duration by nonspecific blockade of K+ channels.
A. I only
B. II only
C. I and II only
D. II and III only
E. I,II and III
I and II only
The following drug is considered to be the most effective in the prevention of ischemic episodes in patients with angina.
A. Sodium nitroprusside
B. Isosorbide dinitrate
C. Propranolol
D. Amlodipine
Propranolol
The diuretic agent that conserves the K+ ions in the body
A. Triamterene
B. Bumetanide
C. Hydrochlorothiazide
D. Furosemide
Triamterene
A case of a 60 year-old male patient with developed gynecomastia and erectile dysfunction due to the treatment of this particular diuretic agent.
A. Hydrochlorothiazide
B. Spironolactone
C. Triamterene
D. Furosemide
Spironolactone
The following statements are true for Lidocaine.
I. Extensive first-pass hepatic metabolism
II. Plasma clearance is increased in liver damage
III. Volume of distribution is decreased in liver damage
A. I only
B. II only
C. I and II only
D. II and III only
E. I,II and III
I only
The following are the results of vasodilating activity of Sodium nitroprusside
I. Activation of guanylyl cyclase
II. Increased intracellular cGMP
III. Decreased intracellular cGMP
A. I only
B. II only
C. I and II only
D. II and III only
E. I,II and III
I and II only
The following are the mechanism of actions of most of the drugs with vasodilating actions
I. Increasing cGMP
II. Promoting depolarization of the vascular smooth muscles
III. Increasing intracellular Ca2+
A. I only
B. II only
C. I and II only
D. II and III only
E. I,II and III
I only
What is the administration rate of theophylline, representing 0.8 of the administered dose,
when aminophylline is infused at 75 mg/hr?
A. 40 mg/h
B. 60 mg/h
C. 50 mg/h
D. 70 mg/h
60 mg/h
Four hours following the IV administration of a drug, a patient (70 kg) was found to have a
plasma concentration of 5.6 mcg/ml. Assuming the Vd is 10 % of body weight, what is the
amount of drug in mg, present in body fluids?
A. 35.7
B. 39.2
C. 37.5
D. 32.9
39.2
The rate of zero-order reactions
A. changes constantly
B. holds only for light catalyzed reactions
C. is independent of temperature
D. holds only for radioactive compounds
E. in independent of concentration
in independent of concentration
What will result if the distribution of drugs is slower than the processes of biotransformation
and elimination?
A. high blood levels of drug
B. potentiation
C. low blood levels of drug
D. failure to attain diffusion equilibrium
E. synergism
failure to attain diffusion equilibrium
Which of the following drugs undergoes marked hydrolysis in the GI tract?
A. ASA
B. Hydrocortisone
C. Penicillin G
D. Chlortetracycline
E. Acetaminophen
Penicillin G
Which of the following factors may make it necessary to give lower doses of drugs to geriatric patients?
A. reduced enzyme activity
B. reduced kidney function
C. enhanced absorption
D. A and B only
E. A, B and C
A and B only
A prime consideration in biopharmaceutics is a drug “bioavailability” which refers to the relative amount of drug that reaches the relative amount of drug that reaches the
A. small intestine
B. liver
C. stomach
D. kidneys
E. systemic circulation
systemic circulation