In response to the patient's question about how to know whether drugs are safe, the nurse explains that all medications undergo rigorous scientific testing controlled by what organization?
Food and Drug Administration (FDA)
Drug Enforcement Agency (DEA)
Centers for Disease Control and Prevention (CDC)
Joint Commission on Accreditation of Healthcare Organizations (JCAHO)
The Correct Answer is A
A. The FDA is responsible for regulating and ensuring the safety and efficacy of drugs, medical devices, and other health-related products. All medications must undergo rigorous scientific testing and approval processes overseen by the FDA before they can be marketed to the public.
B. The DEA regulates controlled substances and enforces laws related to drug abuse, but it does not control the scientific testing of medications.
C. The CDC focuses on public health and disease prevention, not the regulation or testing of medications.
D. The Joint Commission accredits healthcare organizations but does not directly oversee the scientific testing of medications.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is C
Explanation
A. Capsules generally take longer to dissolve than liquid suspensions and thus do not provide the fastest onset of action.
B. Enteric-coated pills are designed to dissolve in the small intestine rather than the stomach, which can delay the onset of action. They are typically used to protect the drug from stomach acid or to prevent stomach irritation, not for rapid action.
C. Liquid suspensions are absorbed more quickly than solid forms of medication because they do not need to dissolve first, allowing for faster onset of action.
D. Tablets take longer to dissolve than liquid forms and may not provide as rapid an effect as a liquid suspension.
Correct Answer is C
Explanation
A. While pediatric doses are often weight-based, this does not fully account for differences in drug metabolism and effects in children. Pediatric drug safety requires specific testing beyond weight comparisons to adults.
B. Relying on repeated use over time to determine safety is not an evidence-based approach. Drug approval for pediatric use requires formal clinical trials to establish safety and efficacy.
C. The U.S. FDA and other regulatory agencies require that drugs intended for pediatric use undergo clinical trials specifically designed to assess safety, efficacy, and appropriate dosing in children. This ensures that medications are appropriately tested before being marketed for pediatric patients.
D. While some post-marketing studies may include children, initial approval for pediatric use requires pre-market clinical testing. Relying solely on post-marketing studies does not ensure comprehensive safety data before widespread pediatric use.
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