Final answer:
Pharmacies must adhere to FDA regulations, which include proper licensing and potentially limiting sales of hypodermic syringes or needles to those with medical prescriptions. While regulations protect the public, some individuals, such as those requiring timely treatment or at-risk groups needing access to clean needles, might be disadvantaged.
Step-by-step explanation:
a pharmacy to sell a *hypodermic syringe or needle*_:
The requirements for a pharmacy to sell hypodermic syringes or needles vary by state and jurisdiction. Generally, pharmacies must comply with FDA regulations, which include proper licensing, record-keeping, and sometimes customer restrictions based on the intended use. For instance, pharmacies might only sell syringes to those with a medical prescription or limit the quantity of syringes sold without prescription.
The winners in this regulated system are the general public, who are protected from the harm of unsafe medical products. However, the losers—or those who do not benefit—from these regulations are potentially the patients who need timely access to innovative treatments but face delays due to the long testing and approval process. Additionally, groups such as drug addicts who might need clean needles to reduce the risk of infections or health care workers like phlebotomists and dentists who face higher needle stick risks may also be affected.