A. Intravenous
B. Oral
C. Rectal
D. Transcutaneous
B. Oral
A. Intramuscular
B. Intravenous
C. Oral
D. Rectal
E. Subcutaneous
B. Intravenous
Rationale:
Intravenous (IV) administration into the circulatory system offers the most direct route with effective delivery to their sites of action.
A. Intramuscular
B. Intravenous
C. Rectal
D. Subcutaneous
C. Rectal
A. Decline
B. Spuriously decline
C. Rise
D. Spuriously rise
C. Rise
Rationale:
Serum concentrations rise when the rate of absorption exceeds distribution and elimination.
The concentration declines as the rate of elimination and distribution exceeds absorption.
The rate of elimination can only be determined after absorption and distribution are complete.
A. Declines
B. Spuriously declines
C. Rises
D. Spuriously rises
A. Declines
A. Amount of WBCs in the specimen
B. Presence of glucose in the specimen
C. Timing of specimen collection
D. Volume of specimen
C. Timing of specimen collection
Rationale:
In general, trough concentrations for most drugs are drawn right before the next dose; peak concentrations are drawn 1 hour after an orally administered dose.
A. Expectorated sputum
B. Gastric fluid
C. Serum or plasma
D. Urine
C. Serum or plasma
Rationale:
Serum or plasma is the specimen of choice for the determination of circulating concentrations of most drugs.
Heparinized plasma is suitable for most drug analysis. The calcium-binding anticoagulants add a variety of anions and cations that may interfere with analysis or cause a drug to distribute differently between cells and plasma. As a result, ethylenediaminetetracetic acid (EDTA), citrated and oxalated plasma are not usually acceptable specimens.
A. Aminoglycoside
B. Digixon
C. Procainamide
D. Quinidine
A. Aminoglycoside
Rationale:
Aminoglycosides are a group of chemically related antibiotics used for the treatment of infections with gram-negative bacteria that are resistant to less toxic antibiotics.
A. Carbamazepine
B. Phenobarbital
C. Phenytoin
D. Valproic acid
B. Phenobarbital
A. Digoxin
B. Lithium
C. Phenytoin
D. Theophylline
B. Lithium
A. Cyclosporine
B. Phenytoin
C. Sirolimus (rapamycin)
D. Tacrolimus
B. Phenytoin
Rationale:
AKA (Dilantin) commonly used treatment for seizures
A. Clozapine
B. Ethosuximide
C. Methotrexate
D. Procainamide
C. Methotrexate
A. Poisons
B. Toxins
C. Xenobiotics
C. Xenobiotics
A. Poisons
B. Toxins
C. Xenobiotics
A. Poisons
A. Brain
B. Heart
C. Kidney
D. Liver
D. Liver
A. Greater than 0.5
B. Greater than 1.0
C. Greater than 1.5
D. Greater than 2.0
D. Greater than 2.0
A. Butyl alcohol
B. Ethyl alcohol
C. Isopropyl alcohol
D. Methyl alcohol
C. Isopropyl alcohol
A. Decrease amount of oxygen delivered to tissue
B. Increase amount of oxygen delivered to tissue
C. Variable amount of oxygen delivered to tissue
D. Normal amount of oxygen delivered to tissue
A. Decrease amount of oxygen delivered to tissue
A. Corticosteroids
B. Intravenous immunoglobulins
C. Platelet transfusion
D. 100% oxygen therapy
D. 100% oxygen therapy
A. Nephrotoxicity
B. Hepatotoxicity
C. Ototoxicity
D. Neurotoxicity
B. Hepatotoxicity
A. Amphethamine
B. Cannabinoid
C. Metamphetamine
D. Methylenedioxymethylamphetamine
D. Methylenedioxymethylamphetamine
A. 0.5 to 1 hour
B. 1 to 2 hours
C. 7 to 8 hours
D. 8 to 9 hours
D. 8 to 9 hours
Rationale:
● Half-life of ecstasy: 8 to 9 hours
● Half-life of THC: 1 day after a single use and 3 to 5 days in chronic, heavy consumers
● Half-life of cocaine: 0.5 to 1 hour
● Half-life of benzoylecgonine: 4 to 7 hours
A. 0.5 to 1 hour
B. 1 to 2 hours
C. 7 to 8 hours
D. 8 to 9 hours
A. 0.5 to 1 hour
A. Codeine
B. Heroin
C. Morphine
D. Opium
B. Heroin
Rationale:
OPIATES:
The naturally occurring substances include opium, morphine, and codeine.
Heroin, hydromorphone (Dilaudid), and oxycodone (Percodan) are chemically modified forms of the naturally occurring opiates.
Meperidine (Demerol), methadone (Dolophine), propoxyphene (Darvon), pentazocine (Talwin), and fentanyl (Sublimaze) are the common synthetic opiates.