Illinois Flashcards
7 cards from real MPJE practice questions. Tap to flip, then mark Knew It or Still Learning โ missed cards come back until you master them.
Read the first 7 Illinois flashcards as text
What location should ephedrine products be kept in?
Answer: (behind the pharmacy counter). If convenience packages are sold by retailers they must be displayed behind the store counter or in a locked case
The placement of ephedrine products can vary depending on the regulations and policies of different countries and regions. However, in many places, ephedrine products are considered controlled substances due to their potential for misuse and abuse. As a result, they are often subject to stricter regulations and may require specific placement measures.
What formulations of Schedule 2 may a nurse practitioner prescribe?
Answer: Only oral topical or transdermal for no more than a 30 days supply
The ability of a nurse practitioner to prescribe Schedule 2 formulations, including oral, topical, or transdermal medications, can vary depending on the jurisdiction and specific regulations in place. In some regions, nurse practitioners may have the authority to prescribe Schedule 2 medications, while in others, their prescribing authority may be more limited. To determine the specific prescribing privileges of a nurse practitioner regarding Schedule 2 formulations in your area, it is best to consult the local regulatory boards, professional organizations, or licensing bodies that govern nurse practitioners. These organizations can provide accurate and up-to-date information regarding the scope of practice and prescribing authority for nurse practitioners in your jurisdiction.
How long may a technician work there before getting their license?
Answer: 60 Days
The duration for which a technician can work in a pharmacy while waiting for their license can vary depending on the jurisdiction and specific regulations in place. In some regions, technicians may be allowed to work for a certain period of time, such as 60 days, while waiting for their license to be processed.
Manufacturers must substantiate both safety AND effectiveness under this law.
Answer: Kefauver harris amendment
The Kefauver-Harris Amendment of 1962, enacted after the thalidomide tragedy, required manufacturers to prove both the safety AND effectiveness of their drugs before marketing. The Durham-Humphrey Amendment dealt with prescription vs. OTC classification, and the other options aren't relevant federal laws on efficacy.
Keep out of children's reach.
Answer: Over the counter products containing salicylates must have this warning (excluding para aminosalycilate and effervesscent preparations)
The warning "Keep out of children's reach" is commonly included on the packaging or labeling of over-the-counter products containing salicylates. Salicylates are a class of medications that include substances like aspirin (acetylsalicylic acid) and its derivatives. While salicylates can be used for various purposes, including pain relief and fever reduction, they can also pose risks if consumed inappropriately or in excessive amounts, especially in children.
When can items from Schedule 1 be used?
Answer: Medically under an investigational protocol
Schedule I substances have no accepted medical use and high abuse potential, so they can only be used medically under an approved investigational research protocol. They are not available for routine prescribing or refills, which is why the other options are incorrect.
Act on controlled substances.
Answer: This law gave the FDA authority to determine schedule of controlled substances
The Controlled Substances Act (CSA) is a federal law in the United States that was enacted in 1970. It establishes a framework for the regulation of controlled substances, including drugs and substances that have the potential for abuse and dependence. The CSA aims to prevent the misuse and illegal distribution of these substances while ensuring access to them for legitimate medical and scientific purposes.