(A) Cannot be used with unconsciousness patients
(B) Generally results in a less accurate dosage than oral administration
(C) Usually produces a more rapid response than oral administration use
(D) Is too slow for emergency

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(A) Cannot be used with unconsciousness patients
(B) Generally results in a less accurate dosage than oral administration
(C) Usually produces a more rapid response than oral administration use
(D) Is too slow for emergency
(A) Rectal
(B) Oral
(C) Sublingual
(D) Inhalation
(A) Pretty fast absorption
(B) A drug is exposed to gastric secretion
(C) A drug is exposed more prominent liver metabolism
(D) A drug can be administrated in a variety of doses
(A) Fast onset of effect
(B) Absorption depends on GI tract secretion and motor function (✓)
(C) A drug reaches the blood passing the liver
(D) The sterilization of medicinal forms is obligatory
(A) Sublingual
(B) Oral
(C) Intravenously
(D) Intramuscula
(A) Oral
(B) Transdermal
(C) Rectal (✓)
(D) Intraduodenal
(A) Rheological parameters of blood
(B) Amount of a substance obtained orally and quantity of intakes
(C) Extent of absorption and hepatic first-pass effect
(D) Glomerular filtration rate
(A) Plasma protein binding degree of substance
(B) Permeability through the brain-blood barrier
(c) Fraction of an uncharged drug reaching the systemic circulation following any route administration
(D) Amount of a substance in urine relative to the initial doze
(A) Transport of drugs trough a membrane by means of diffusion
(B) Transport without energy consumption
(C) Engulf of drug by a cell membrane with a new vesicle formation
(D) Transport against concentration gradient (✓)
(A) Low ability to penetrate through the cell membrane lipids (✓)
(B) Penetrate through membranes by means of endocytosis
(C) Easy permeation through the blood-brain barrier
(D) High reabsorption in renal tubules