13 Principles of Pharmacology and Emergency Medications Flashcards
Which drugs were developed to treat rare chronic diseases, such as leprosy and hemophilia, that will not be profitable for the drug manufacturing company? A. Next-generation C. Second-class B. Nonmarketable D. Orphan
D
Drugs are derived from five major sources. Among them are: A. Water, air, and minerals B. Minerals, chemicals, and water C. Plants, animals, and microorganisms D. Food products, ambient air, and synthetics
C
What is the study of how a drug acts on a living organism? A. Pharmaceutics C. Pharmacodynamics B. Pharmacokinetics D. Pharmacodistribution
C
Which is this drug’s generic name, as approved by the Food and Drug Administration? A. Demerol B. Meperidine hydrochloride C. Meperidine hydrochloride, USP D. Ethyl 1-methyl-4-phenylisoni-pecotate hydrochloride
B
Which is the drug’s chemical name? A. Demerol B. Meperidine hydrochloride C. Meperidine hydrochloride, USP D. Ethyl 1-methyl-4-phenylisoni-pecotate hydrochloride
D
Which is the drug’s trade name, as designated by the company that sells the medication? A. Demerol B. Meperidine hydrochloride C. Meperidine hydrochloride, USP D. Ethyl 1-methyl-4-phenylisoni-pecotate hydrochloride
A
Which is the drug’s official name? A. Demerol B. Meperidine hydrochloride C. Meperidine hydrochloride, USP D. Ethyl 1-methyl-4-phenylisoni-pecotate hydrochloride
C
Which is true in regards to generic drugs?
A.
Have 75% to 90% of the strength of the trade-name drugs
B.
Have the same therapeutic efficacy as the trade-name version
C.
Are produced by the government; trade-name drugs are produced by private industry
D.
Are typically the repackaged versions of trade-name drugs that have exceeded their shelf life
B
Following a drug name are the letters USP—what do these letters represent? A. Name of the manufacturer B. Route of administration of the drug C. Official publication in which the drug is listed D. City in which the drug was manufactured
C
Which would provide the most up-to-date information on a drug? A. The Physicians’ Desk Reference B. American Medical Association Drug Evaluation C. The American Hospital Formulary Service D. Internet Web sites such as MedLine Plus
D
Which 1906 act by the United States Congress was enacted to protect the public from mislabeled or adulterated drugs? A. The National Formulary Act C. The Controlled Substance Act B. The Pure Food and Drug Act D. The United States Pharmacopeia Act
B
Which agency is responsible for the regulation of biological products such as viruses and therapeutic serums? A. The Public Health Service C. The Federal Trade Commission B. The Drug Enforcement Agency D. The Food and Drug Administration
A
Which agency is responsible for the regulation of biological products such as viruses and therapeutic serums? A. The Public Health Service C. The Federal Trade Commission B. The Drug Enforcement Agency D. The Food and Drug Administration
C
Which is an enteral route of administration? A. Rectal C. Sublingual B. Intramuscular D. Intravenous
A
Which is an advantage of the enteral route? A. Fast absorption of drugs C. Safety B. Reliable onset of action D. Immediate distribution
C
Which location does most absorption of drugs administered by the enteral route occur? A. Mucosal lining of the mouth C. Small intestine B. Stomach D. Large intestine
C
Which describes sublingual drug administration?
A.
Injected into the tongue
B.
Placed under the tongue
C.
Rubbed on the skin inferior to the mandible
D.
Placed between the tongue and the roof of the mouth
B
Drugs administered rectally: A. Have dependable absorption rates B. Can be affected by rectal contents C. Completely bypass first-pass metabolism D. Have absorption rates identical to those of oral medications
B
Parenteral drugs are administered through which route? A. GI tract C. Injection B. Mouth D. Skin
C
What is the maximum volume of injected medication for subcutaneous administration?
A.
5.0 mL
B.
0.5 mL
C.
The same as that for intramuscular administration
D.
Twice the amount as that for intramuscular administration
B
Which area is subcutaneous injection introduced? A. Epidermis C. Fat and connective tissue B. Dermis D. Muscle
C
An intramuscular injection:
A.
Is absorbed more slowly than an orally administered medication
B.
Is absorbed more quickly than a subcutaneous injection
C.
Has the same rate of absorption as an intravenous injection
D.
Has the same rate of absorption as a subcutaneous injection
B
Which route has the most rapid onset of action? A. Subcutaneous C. Intravenous B. Intramuscular D. Intradermal
D
Intradermal routes of administration are intended primarily for which purpose? A. Allergy testing C. Systemic distribution B. Rapid onset of action D. Vaccinations
A
Intraosseous medications are delivered into which location? A. Bone marrow cavity C. Periosteum of the bone B. Cortex of the bone D. Blood vessels surrounding bones
A
The onset of action of medications administered by the intraosseous route is equivalent to \_\_\_\_\_ administration. A. Intradermal C. Intramuscular B. Subcutaneous D. Intravenous
D
Which drugs may be administered via an endotracheal tube?
A.
Normal saline, lactated Ringer’s, and D5W
B.
Sodium bicarbonate, calcium, and dextrose
C.
Epinephrine, lidocaine, atropine, naloxone, and vasopressin
D.
Dopamine, epinephrine, lidocaine, and atropine
C
If the normal intravenous dose of a medication is 5 mg, how much would you administer if you chose to give the medication via the endotracheal tube (assuming the medicine is compatible with this route)? A. 1 mg C. 10 mg B. 5 mg D. 25 mg
C
Endotracheal medications should be diluted in which solution? A. 50 mL of D5W C. 100 mL of normal saline B. 10 mL of normal saline D. 20 mL of Bronkaid Mist
B
Endotracheal administration of drugs is recommended at which point?
A.
Any time a patient is intubated
B.
Whenever a patient requires a medication compatible with this route
C.
When an IV or IO line is not available
D.
When the medications are intended to act on lung tissue
C
What are the most commonly inhaled medications? A. Bronchodilators C. Antihypertensives B. Vasoconstrictors D. Narcotic antagonists
A
Lipid-soluble compounds for topical application:
A.
Cannot be absorbed through the skin
B.
Should not be applied unless no other routes are available
C.
Are rapidly absorbed through the skin
D.
Will cause burns to the skin if applied for too long
C
What effect will diarrhea have on a medication absorbed primarily in the small intestine?
A.
None of the medication will be absorbed.
B.
The medication will be absorbed much more quickly in this liquid environment.
C.
There will be no change in absorption because diarrhea affects the large intestine only.
D.
The medication will have decreased exposure and therefore decreased absorption.
D
The pH of the small intestine is greater than the pH of the stomach. Based on this fact, which choice can be assumed?
A.
Acidic drugs will not be absorbed in the stomach.
B.
Alkaloid drugs will be absorbed quickly in the stomach.
C.
Alkaloid drugs will be absorbed more quickly in the small intestine than in the stomach.
D.
Alkaloid drugs will be absorbed more quickly in the stomach than in the small intestine.
C
What study refers to how a body handles a drug over time? A. Pharmaceutics C. Pharmacodynamics B. Pharmacokinetics D. Pharmacodistribution
B
Which is the science of dispensing drugs? A. Pharmaceutics C. Pharmacodynamics B. Pharmacokinetics D. Pharmacodistribution
A
The rate and extent of drug absorption depends on six factors. Among these are:
A.
The classification of the drug, the pH of the drug, and the drug concentration
B.
The classification of the drug, the temperature of the drug, and the solubility of the drug
C.
The blood flow to the site of administration, the drug concentration, and the pH of the drug environment
D.
The blood flow to the site of administration, the temperature of the drug, and the solubility of the drug
C
Drug absorption refers to the movement of the drug from the:
A.
Entry site to the general circulation
B.
Entry site to the target organ or tissue
C.
Entry site to the organ of drug metabolism
D.
Target organ or tissue to the organ of drug metabolism
A
Which is true of drugs absorbed in the upper GI tract versus drugs absorbed in the lower GI tract?
A.
Drug absorption is slower in the upper GI tract.
B.
Larger doses are required for the desired effect if the drug is absorbed in the upper GI tract.
C.
Drugs absorbed in the upper GI tract are routed through the liver before entering the general circulation.
D.
Drugs absorbed in the upper GI tract are not subject to first-pass metabolism.
D
Most intravenous injections should be administered:
A.
As a maintenance infusion
B.
Slowly to help prevent an adverse reaction
C.
As a bolus to prevent medication stagnation
D.
Quickly to help prevent the formation of an embolism
B
Which is correct regarding drug distribution and absorption?
A.
Water-soluble and lipid-soluble drugs readily cross the cell membrane.
B.
Lipid-insoluble drugs readily cross the cell membrane.
C.
Lipid-soluble drugs readily cross the cell membrane.
D.
Water-soluble drugs readily cross the cell membrane.
C
Where is a drug generally distributed first? A. Target organ C. Muscle B. Heart D. Fat
B
What are the single layers of capillary endothelial cells that line the blood vessels entering the central nervous system? A. Blockade C. Barrier to distribution B. Protective lining D. Blood-brain barrier
D
What is a drug conversion to a metabolite called? A. Excretion C. Sublimation B. Elimination D. Biotransformation
D
What is/are the primary site(s) of drug metabolism? A. Liver C. Spleen B. Lungs D. Kidneys
A
First-pass metabolism:
A.
Reduces the amount of drug available for distribution
B.
Commonly occurs in parenterally administered drugs
C.
Increases the ability of drugs to affect target organs
D.
Is desirable for drugs that are highly concentrated
A
Which is/are the primary organ(s) of drug excretion? A. Liver C. Spleen B. Lungs D. Kidneys
D
The term clearance refers to the complete: A. Binding of a drug to a protein B. Removal of a drug by the kidneys C. Metabolism of a drug by the liver D. Absorption of a drug by the target tissues
B
A drug is considered to be eliminated from the body after what occurs? A. 20 minutes B. Less than 5% of the drug remains in the body C. The patient is no longer showing effects D. The drug has reached its half-life
B
Which is a product of the endocrine portion of the pancreas? A. Iodine C. Synovial fluid B. Glucagon D. Digestive enzymes
B
Which drug stimulates the liver to break down glycogen? A. Insulin C. Glucagon B. Bilirubin D. Levothyroxine
C
Which is the primary hormone that regulates glucose metabolism? A. Insulin C. Thyroxine B. Glycogen D. Levothyroxine
A
A drug that interacts with a receptor to stimulate a response is known as a(n) \_\_\_\_\_. A. Actor C. Promoter B. Agonist D. Proactive
B
You would expect a drug with a fast rate of dissolution to: A. Be absorbed quickly into the body B. Expire soon after it is manufactured C. Lose its effectiveness quickly once it enters the body D. Have a very short half-life
A
What occurs as the levels of an unbound drug decrease?
A.
More drug is released from plasma protein binding.
B.
More drug is bound to tissues to preserve the circulating level.
C.
Less drug is released into the bloodstream to allow for elimination.
D.
Less drug is released from plasma protein binding.
A
Reactive sites within cells or on cellular surfaces where a drug may bind are called: A. Locks C. Keys B. Binders D. Receptors
D
In parasympathetic nervous action, the binding of acetylcholine at nicotinic receptors produces which result of the effector organ? A. Blocking C. Inhibition B. Relaxation D. Excitatory response
D
The binding of acetylcholine at muscarinic receptors produces which effect?
A.
An excitatory response in the effector organ
B.
An inhibition of the effector organ
C.
Either an excitatory response or an inhibition, depending on the tissues involved
D.
A massive release of muscarine into the target organ
C
Which response appropriately describes the effects atropine has on the parasympathetic nervous system?
A.
Blocking muscarinic receptor sites in the heart, thus slowing the heart rate
B.
Stimulating both muscarinic and nicotinic receptor sites in the heart, thus slowing the heart rate
C.
Stimulating muscarinic receptor sites while blocking the nicotinic receptor sites, thus slowing the heart rate
D.
Blocking both muscarinic and nicotinic receptor sites for the heart, causing paralysis
A
Curare is a drug that blocks parasympathetic tone. The drug acts on which receptor sites?
A.
Nicotinic, causing paralysis
B.
Adrenergic, causing paralysis
C.
Nicotinic, causing a rapid heart rate and subsequent myocardial infarction
D.
Muscarinic, causing a rapid heart rate and subsequent myocardial infarction
A
Although norepinephrine will bind to both postganglionic adrenergic receptor sites, it has an affinity for which receptors? A. Beta C. Nicotinic B. Alpha D. Muscarinic
B
Epinephrine is an adrenergic substance that is a(n): A. Enzyme produced by the kidneys B. Enzyme produced in the cerebral cortex C. Hormone produced by the adrenal medulla D. Hormone produced by the medulla oblongata
C