ACTUAL COMPLETE REAL EXAM QUESTIONS
AND CORRECT ANSWERS (VERIFIED ANSWERS)
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Nurse practitioner prescriptive authority is regulated by:
A. The National Council of State Boards of Nursing
B. The U.S. Drug Enforcement Administration
C. The State Board of Nursing for each state
D. The State Board of Pharmacy - ANSWER-C. The State Board
of Nursing for each state
Cardiac defects are a known Type D adverse drug reaction to
lithium. Lithium causes a Type D adverse drug reaction
because it is:
A. An immunosuppressant
B. A carcinogen
C. A teratogen
D. An antiseizure medication - ANSWER-C. A teratogen
Immunomodulators such as azathioprine may cause a delayed
adverse drug reaction known as a Type D reaction because
they are known:
A. Teratogens
B. Carcinogens
C. To cause hypersensitivity reactions
,D. Hypothalamus-pituitary-adrenal (HPA) axis suppressants -
ANSWER-B.
Carcinogens
A 24-year-old male received multiple fractures in a motor
vehicle accident that
required significant amounts of opioid medication to treat his
pain. He is at risk
for Type __ adverse drug reaction when he no longer
requires the opioids.
A.
A
B.
C
C.
E
D. G - ANSWER-
C. E
rugs that may cause a Type E adverse drug
reaction include:
A. Beta blockers
B.
Immunomodulators
C. Antibiotics
D. Oral contraceptives - ANSWER-A. Beta
blockers
,Unexpected failure of drug therapy is a Type __ adverse
drug reaction, commonly caused by____. A. B;
cytotoxic hypersensitivity
B. B; idiosyncratic response
C. C; cumulative effects of drug
D. F; drug-drug interaction - ANSWER-D. F; drug-drug
interaction
Clopidogrel treatment failure may occur when it is co-
administered with
omeprazole, known as a Type __ adverse
drug reaction.
A.
A
B.
C
C.
E
D. F - ANSWER-
D. F
The Pediatric Research Equity Acts requires:
A. All children be provided equal access to drug research
trials
B. Children to be included in the planning phase of new drug
development C. That pediatric drug trials guarantee
children of multiple ethnic groups are included
, D. All applications for new active ingredients, new indications,
new dosage forms, or new routes of administration require
pediatric studies - ANSWER-D.
All applications for new active ingredients, new indications,
new dosage forms,
or new routes of administration require
pediatric studies
The Best Pharmaceuticals for Children Act:
A. Includes a pediatric exclusivity rule which extends the patent
on drugs studied in children
B. Establishes a committee that writes guidelines for pediatric
prescribing
C. Provides funding for new drug development aimed at
children
D. Encourages manufacturers specifically to develop pediatric
formulations - ANSWER-B. Establishes a committee that
writes guidelines for pediatric prescribing
The developmental variation in Phase I enzymes has what
impact on pediatric prescribing?
A. None, Phase I enzymes are stable throughout childhood.
B. Children should always be prescribed lower than adult doses
per weight due to low enzyme activity until puberty.
C. Children should always be prescribed higher than adult
doses per weight due to high enzyme activity.
D. Prescribing dosages will vary based on the developmental
activity of each enzyme, at times requiring lower than adult
doses and other times higher than adult doses based on the