ام سى كيو فارما
3 مشترك
صفحة 1 من اصل 1
ام سى كيو فارما
دول شوية ام سى كيو فارما من كتاب القسم بتاع السنة اللى فاتت
عن ال pharmacokinetics
عينى اتمققت على ما كتبتهم
ربنا يقدرنى و اكملهم و انشاء الله اول ما ينزل الجديد هرفعه بأعلى جودة
1- the following is NOT TRUE concerning diffusion of drugs across cell membranes
a- most drugs cross cell membranes primairly by passive diffusion
b- diffusion is dependent on the drug being lipid soluble i.e exists mainly in non-ionized form
c- acidification of urine hastens excretion of weakly basic drugs
d- aspirin is mainly ionized in the empty stomach thus crosses cell membranes of mucosal cells to be trapped inside resulting in peptic ulceration
====================
2- important factors which may govern diffusion of drugs across cell membranes
a- pKa value of the drug
b- pH of the medium
c- lipid solubility of the drug
d- all of the above
====================
3- the first pass effect is most likely to occur if the drug is given
a- orally
b- rectally
c- subcutaneously
d- sublingually
e- A & C
=======================
4- which of the following drugs is/are wrongly matched to the site of first pass metabolism
a- estrogen / hepatic
b- nicotine / pulmonary
c- nitroglycerin / intestinal
d- propranolol / hepatic
e- A & C
======================
5- drugs reducing hepatic 1st pass metabolism
a- rifampicin
b- propranolol
c- erythromycin
d- B & C
=======================
6- which of the following routes of administration allows for titrating dose of a drug with the response
a- slow intravenous infusion
b- transdermal
c- sublingual
d- inhalation
e- A & D
=====================
7- drugs with variable bioavailability among different dosage forms are
a- digoxin
b- aspirin
c- phenytoin
d- A & B
=====================
8- a main determinant of bioavailability (F) following oral administration is
a- hepatic extraction ratio (E)
b- elimination rate constant (Ke)
c- bioequivalence
d- none of the above
========================
9- lipophilicity reduces
a- absorption
b- volume of distribution (Vol)
c- hepatic elimination
d- renal excretion
=====================
10- drugs with small volume of distribution are characterized by
a- limited tissue uptake
b- dialysis is useful in toxicity
c- their Vd cannot be less than 5 liters
d- all of the above
e- A & B
====================
11- the following characteristics of a drug tends to reduce its volume of distribution
a- low ionization at physiological pH
b- high lipid solubility
c- high tissue binding
d- high plasma proteins binding
e- A & C
=====================
12- the following drugs do not act readily cross to the CNS in meningitis
a- streptomycin
b- rifampicin
c- tetracycline
d- penicillins
e- A & C
=====================
13- the following drugs do not readily cross to CNS
a- dopamine
b- levodopa
c- atropine
d- ncostgmine
e- A & D
=====================
14- the following is a phase II reaction
a- reduction
b- hydrolysis
c- acetylation
d- oxidation
=====================
15- microsomal enzymes include
a- dehydrogenase
b- esterases
c- CY P450 enzyme system
d- glucouryl transferase
e- C & D
======================
16- in which organ is the majority of cytochrome P450 most highly expressed
a- brain
b- liver
c- lung
d- kidney
e- small intestine
=======================
عن ال pharmacokinetics
عينى اتمققت على ما كتبتهم
ربنا يقدرنى و اكملهم و انشاء الله اول ما ينزل الجديد هرفعه بأعلى جودة
1- the following is NOT TRUE concerning diffusion of drugs across cell membranes
a- most drugs cross cell membranes primairly by passive diffusion
b- diffusion is dependent on the drug being lipid soluble i.e exists mainly in non-ionized form
c- acidification of urine hastens excretion of weakly basic drugs
d- aspirin is mainly ionized in the empty stomach thus crosses cell membranes of mucosal cells to be trapped inside resulting in peptic ulceration
====================
2- important factors which may govern diffusion of drugs across cell membranes
a- pKa value of the drug
b- pH of the medium
c- lipid solubility of the drug
d- all of the above
====================
3- the first pass effect is most likely to occur if the drug is given
a- orally
b- rectally
c- subcutaneously
d- sublingually
e- A & C
=======================
4- which of the following drugs is/are wrongly matched to the site of first pass metabolism
a- estrogen / hepatic
b- nicotine / pulmonary
c- nitroglycerin / intestinal
d- propranolol / hepatic
e- A & C
======================
5- drugs reducing hepatic 1st pass metabolism
a- rifampicin
b- propranolol
c- erythromycin
d- B & C
=======================
6- which of the following routes of administration allows for titrating dose of a drug with the response
a- slow intravenous infusion
b- transdermal
c- sublingual
d- inhalation
e- A & D
=====================
7- drugs with variable bioavailability among different dosage forms are
a- digoxin
b- aspirin
c- phenytoin
d- A & B
=====================
8- a main determinant of bioavailability (F) following oral administration is
a- hepatic extraction ratio (E)
b- elimination rate constant (Ke)
c- bioequivalence
d- none of the above
========================
9- lipophilicity reduces
a- absorption
b- volume of distribution (Vol)
c- hepatic elimination
d- renal excretion
=====================
10- drugs with small volume of distribution are characterized by
a- limited tissue uptake
b- dialysis is useful in toxicity
c- their Vd cannot be less than 5 liters
d- all of the above
e- A & B
====================
11- the following characteristics of a drug tends to reduce its volume of distribution
a- low ionization at physiological pH
b- high lipid solubility
c- high tissue binding
d- high plasma proteins binding
e- A & C
=====================
12- the following drugs do not act readily cross to the CNS in meningitis
a- streptomycin
b- rifampicin
c- tetracycline
d- penicillins
e- A & C
=====================
13- the following drugs do not readily cross to CNS
a- dopamine
b- levodopa
c- atropine
d- ncostgmine
e- A & D
=====================
14- the following is a phase II reaction
a- reduction
b- hydrolysis
c- acetylation
d- oxidation
=====================
15- microsomal enzymes include
a- dehydrogenase
b- esterases
c- CY P450 enzyme system
d- glucouryl transferase
e- C & D
======================
16- in which organ is the majority of cytochrome P450 most highly expressed
a- brain
b- liver
c- lung
d- kidney
e- small intestine
=======================
mido le roi- مــراقــب قـسـم
- عدد المشاركات : 1407
تاريخ التسجيل : 26/07/2010
المود :
رد: ام سى كيو فارما
على فكرة
موقع الكلية مليان ام سي كيو
موقع الكلية مليان ام سي كيو
Abotreka- مــراقـب عــام
- عدد المشاركات : 8531
البلد : في الشقة اللي قصاد جيرانا
تاريخ التسجيل : 01/07/2010
المود :
رد: ام سى كيو فارما
يا ولكم يا ادمن
ماشى يا تريكة اول ما اخد اليوزر و الباسورد هرفعهم برده
ماشى يا تريكة اول ما اخد اليوزر و الباسورد هرفعهم برده
mido le roi- مــراقــب قـسـم
- عدد المشاركات : 1407
تاريخ التسجيل : 26/07/2010
المود :
صفحة 1 من اصل 1
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