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Pharmacology Demystified

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10<br />

PHASE II: LIMITED CONTROLLED EVALUATION<br />

The purpose of Phase II evaluation is to monitor drug effectiveness and any side<br />

effects. Individuals with the targeted disease participate in this phase of drug<br />

trials. For example, antihypertensive (blood pressure lowering) drugs will be<br />

administered to patients who have hypertension (high blood pressure) to determine<br />

the drug’s effectiveness or optimal dose response range and for side<br />

effects. The number of participants is larger than Phase I trials but usually does<br />

not exceed 100 persons and every effort is made to use only people who have no<br />

other disorders or diseases.<br />

PHASE III: EXTENDED CLINICAL EVALUATION<br />

Phase III drug trials include many physicians and large groups of participants.<br />

When enough information has been collected to justify continued use of the<br />

drug, a New Drug Application (NDA) is submitted to the FDA. Usually, more<br />

than 4 years has passed between the drug’s selection and the filing of the NDA.<br />

Phase IV studies are also called post-marketing follow-up. They are voluntarily<br />

conducted by pharmaceutical companies. These studies continue after the<br />

FDA has approved the drug and often include populations such as pregnant<br />

women, children, and the elderly. Manufacturers can find low-level side effects<br />

or can find that a drug is toxic and must be removed from market. The FDA continues<br />

to monitor new drugs even after they are marketed.<br />

Drugs also undergo tests to determine the possible effects on a fetus. As a result<br />

of these tests, drugs are classified using the following Pregnancy Categories.<br />

Category A<br />

Adequate and well-controlled studies indicate no risk to the fetus in the first<br />

trimester of pregnancy or later.<br />

Category B<br />

Animal reproduction studies indicate no risk to the fetus, however there are no<br />

well-controlled studies in pregnant women.<br />

Category C<br />

CHAPTER 1 An Inside Look at <strong>Pharmacology</strong><br />

Animal reproduction studies have reported adverse effects on the fetus, however<br />

there are no well-controlled studies in humans but potential benefits may indicate<br />

use of the drug in pregnant women despite potential risks.

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