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Adverse drug reactions, (ADRs) usually called side effects, are a long-standing and largely neglected major medical problem. These are not medical errors and occur within the FDA or INFARMED or any other regulatory national board approved dosage and labeling recommendations. The recently reported problems with antidepressant induced teen suicides, the recalls of Vioxx and Baycol shows some of these problems. Research shows that of all the clinical factors such as age, sex, weight, general health and liver function that alter a patient's response to drugs, genetic factors are the most important. Approximately half of the world population has genetic defects that affect how they process these drugs. There are four different types of metabolizers, and we all fall into one of these categories for the variable pathways in Cytochrome P450 (this Cytochrome is responsible for creating the enzymes that process chemicals of all kinds through our bodies.) The easiest way to understand this is to picture a two lane highway.
Who should be tested? Everyone that is considering taking a particular medication should be tested but in particular the elderly and children should do this test.Testing the ElderlyElderly patients have a decreased capacity to detoxify drugs they are taking. Drug interactions are also an important contributor to adverse drug reactions, which makes the aging population vulnerable because of the large number of drugs they are taking. Testing ChildrenFew drugs are tested in children prior to release. Many are used off label in pediatric populations. For example, only Prozac (fluoxetine) has been approved for use in children, yet many others are prescribed off label. While the rate of adverse drug reactions in children is lower than in adults, children with severe medical conditions are the most affected. To read further on the advantages of our pharmacogenetic test please click here. |
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