When patients agree to be part of a study that tests a new drug, they must be thoroughly educated about its possible medical risks. This is referred to as
Drug review
Post-drug approval
Informed consent
A black box warning
Informed consent
Rationale: The thorough education of patients agreeing to be part of a new drug study, and that drug's possible medical risks, is known as informed consent, which also involves the patients giving their written permission to be tested.
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Reactions that release energy are said to be:
A) enderogenic. B) inderogenic. C) exerogenic. D) anderogenic.
A 12-year-old boy was pulled from a river 20 minutes after being swept away by currents. He is unresponsive, not breathing, and shows no signs of life. You should first:
A) rewarm him to a near-normal body temperature. B) perform CPR and attach the AED. C) try to remove water from his lungs. D) notify his family and the medical examiner.
The chronological recording of pertinent facts and observations regarding a patient's health status is known as:
A) medical transcription. B) documentation. C) claims processing. D) encounter form completion.
Loss of hair is called apnea.
Answer the following statement true (T) or false (F)