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In the U.S., the government’s Food and Drug Administration (FDA) must approve any drug – whether it’s prescription or over-the-counter – before it can be sold. The FDA evaluates the safety of a drug by looking at side effects, how it’s manufactured, results of animal testing and clinical trials, and more. The FDA also monitors a drug’s safety after approval.
In broad terms, pharmacodynamics discusses the interactions of chemicals with biological receptors, and pharmacokinetics discusses the absorption, distribution, metabolism, and excretion of chemicals from the biological systems. Pharmacology is not synonymous with pharmacy and the two terms are frequently confused. Pharmacology deals with how drugs interact within biological systems to affect function.
The FDA has determined that several companies are marketing products that look like antimicrobial products available in Mexico. Consumers using the products may believe they will receive the beneficial health effects of an antimicrobial drug. These products may or may not contain antimicrobials, and their use could delay treatment for serious illnesses. These products are not FDA approved to treat, cure or prevent any medical conditions.
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