What is one consequence of using a drug that is made in unsanitary conditions?

Using a drug that is made in unsanitary conditions leads to the drug being classified as adulterated. Adulteration refers to the contamination or degradation of a drug's quality, which can occur due to factors like the presence of harmful microbes, foreign substances, or improper manufacturing processes. In the context of pharmacy and public health, adulterated drugs pose significant risks to patient safety and can lead to harmful health outcomes. Regulatory agencies, such as the FDA, have strict guidelines and inspections to ensure drugs are manufactured in sanitary conditions to prevent such situations. Thus, if a drug is produced under unsanitary conditions, it raises serious concerns about its suitability for patient use and regulatory compliance, justifying why it is characterized as adulterated.