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Pharmacists who prescribe at initial access or manage ongoing therapy must either:

a) Notify the insurance company
b) Refer to a specialist
c) Be on the clinical register
d) Be certified in emergency medicine

User Kulgar
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Final answer:

Pharmacists must obtain a doctorate in pharmacy and state licensing to practice, with their education heavily focused on chemistry and biology. Their responsibilities may include various regulatory obligations and they play a key role in patient medication management and safety. The FDA regulates the pharmaceutical market, which ensures drug safety but can delay access to new treatments.

Step-by-step explanation:

Pharmacists play a crucial role in the healthcare system by dispensing drugs prescribed by physicians, advising on medication usage, and managing ongoing therapy. In the United States, to practice pharmacy, one must obtain a doctorate in pharmacy, followed by state licensing. Their education encompasses extensive knowledge in chemistry and biology, which is essential for understanding the effects of drugs on the human body, ensuring patient safety, and providing effective drug therapy management.

In terms of prescription and therapy management, pharmacists who are responsible for initial prescriptions or ongoing patient therapy management must adhere to certain regulations and practices. Depending on the region and specific laws in place, pharmacists might have different obligations. However, possible requirements could include collaborating with healthcare teams, communicating with insurance companies, maintaining a clinical register, or holding certain certifications. While the question suggests several options, the typical responsibilities do not directly involve notifying an insurance company, referring to a specialist, or being certified in emergency medicine. Rather, this situation usually requires a pharmacist to be part of or recognized by a professional body or association.

The Food and Drug Administration (FDA) plays a significant role in regulating the medicines that pharmacies can sell to ensure safety and efficacy. This regulatory process can lead to prolonged testing periods for drugs before they reach the market. While this regulation protects the public from unsafe medications, it can also result in delayed access to potentially beneficial treatments, which is a downside for those in urgent need of new therapies.

User Stan Sieler
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