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NSG 318 Exam 1 Prep (2025) – 100%
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Resource
Six Rights of Medication Administration
1. Right client
2.Right drug
3.Right dose
4.Right time
5.Right route
6.Right documentation
documentation when administering drugs
The dose
The route
The name of the drug
The nurse's initials or signature
The time and date
The patient has questions about counterfeit drugs. Which factors alert the patient or nurse that a
drug is counterfeit or adulterated? (Select all that apply.)
a. Variations in packaging
b. Unexpected side effects
c. Different taste
d. Different chemical components
e. Different odor
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a. Variations in packaging
b. Unexpected side effects
c. Different taste
The nurse knows the importance of administering the right medication to the patient and that drugs
have many names. It is therefore most important that drugs be ordered by which name?
a. Generic
b. Brand
c. Trade
d. Chemical
generic
What provisions from the Controlled Substances Act of 1970 were designed to remedy drug abuse?
a. The act established treatment and rehabilitation facilities.
b. The act tightened controls on experimental drugs.
c. The act required clinical trial data on drugs.
d. The act required drug companies to give information on off-label use of drugs
The act established treatment and rehabilitation facilities.
two most relevant aspects of Nuremberg Code
the right to be informed
participation is voluntary without coercion
ACCURATE • VERIFIED • 100% CORRECT ANSWERS • LATEST 2025 EDITION
, TESTED, APPROVED & TRUSTED
informed consent
• It is a mutual sharing of information, a process of communication.
• It expresses respect for the person.
• It gains the patient's active involvement in their care.
• It respects the patient's right to self-determination.
Beneficence
the duty to protect research subjects from harm. It involves assessing potential risks and possible
benefits and ensuring the benefits are greater than the risk.
justice
Research must be conducted so that the distribution of benefits and burdens is equitable (i.e.,
research subjects reflect all social classes and racial and ethnic groups).
Good clinical practice consolidated guidelines
an international ethical and scientific quality standard for designing, conducting, monitoring,
auditing, recording, analyzing, and reporting clinical research;
foundation of clinical trials that involve human subjects
genotoxicity
the ability of a compound to damage genetic information in a cell
preclinical trial
phase of clinical trial that is responsible for determining safe parameters of therapeutic dose
ACCURATE • VERIFIED • 100% CORRECT ANSWERS • LATEST 2025 EDITION
NSG 318 Exam 1 Prep (2025) – 100%
Correct Verified Answers | A+ Study
Resource
Six Rights of Medication Administration
1. Right client
2.Right drug
3.Right dose
4.Right time
5.Right route
6.Right documentation
documentation when administering drugs
The dose
The route
The name of the drug
The nurse's initials or signature
The time and date
The patient has questions about counterfeit drugs. Which factors alert the patient or nurse that a
drug is counterfeit or adulterated? (Select all that apply.)
a. Variations in packaging
b. Unexpected side effects
c. Different taste
d. Different chemical components
e. Different odor
ACCURATE • VERIFIED • 100% CORRECT ANSWERS • LATEST 2025 EDITION
,TESTED, APPROVED & TRUSTED
a. Variations in packaging
b. Unexpected side effects
c. Different taste
The nurse knows the importance of administering the right medication to the patient and that drugs
have many names. It is therefore most important that drugs be ordered by which name?
a. Generic
b. Brand
c. Trade
d. Chemical
generic
What provisions from the Controlled Substances Act of 1970 were designed to remedy drug abuse?
a. The act established treatment and rehabilitation facilities.
b. The act tightened controls on experimental drugs.
c. The act required clinical trial data on drugs.
d. The act required drug companies to give information on off-label use of drugs
The act established treatment and rehabilitation facilities.
two most relevant aspects of Nuremberg Code
the right to be informed
participation is voluntary without coercion
ACCURATE • VERIFIED • 100% CORRECT ANSWERS • LATEST 2025 EDITION
, TESTED, APPROVED & TRUSTED
informed consent
• It is a mutual sharing of information, a process of communication.
• It expresses respect for the person.
• It gains the patient's active involvement in their care.
• It respects the patient's right to self-determination.
Beneficence
the duty to protect research subjects from harm. It involves assessing potential risks and possible
benefits and ensuring the benefits are greater than the risk.
justice
Research must be conducted so that the distribution of benefits and burdens is equitable (i.e.,
research subjects reflect all social classes and racial and ethnic groups).
Good clinical practice consolidated guidelines
an international ethical and scientific quality standard for designing, conducting, monitoring,
auditing, recording, analyzing, and reporting clinical research;
foundation of clinical trials that involve human subjects
genotoxicity
the ability of a compound to damage genetic information in a cell
preclinical trial
phase of clinical trial that is responsible for determining safe parameters of therapeutic dose
ACCURATE • VERIFIED • 100% CORRECT ANSWERS • LATEST 2025 EDITION
