Anxiety Treatment: Things You Should Know Before Taking Any Medications
If you are a man who is reasoning about going to a hospital or a clinic to receive a rehabilitation for anxiety as well as other type of reasoning disorders, there are two main methods in which a physician may use. Psycho-therapeutic rehabilitation and pharmacological treatment. As with most other illnesses, it is the physician who normally makes the decision as to which method of rehabilitation should be used. Sometimes, a blend of both methods may be prescribed. Recently, the pharmacological rehabilitation seems to be increasingly adored by more and more doctors despite warnings by many studies and reports that psychiatric medications can cause harmful side-effects. This is the calculate why I am writing this article. It is to tip off you about the risks complex in using pharmacological treatment.
Anxiety Treatment: Things You Should Know Before Taking Any Medications
Pharmacological rehabilitation involves the use of prescribed medications to adjust the level of some chemicals inside a patient's brain. The logic behind this is based on a claim made by pharmaceutical companies that chemical imbalance is the cause of reasoning illness. However, it may surprise you to learn that there is no convincing evidence to support such a claim at all. As a matter of fact, there is no test available today that physician or scientist can use to collate the chemical status of a living person's brain. This is the calculate why you will never have to give a blood or any other kind of samples when you go to a clinic or a hospital for the rehabilitation of reasoning disorder. Amazingly, some doctors are able to decide the level of chemicals inside your brain just by observing and talking to you.
On the other hand, numerous pieces of evidence suggesting harmful effects of these medications continue to emerge. For example, on March 22, 2004, the Fda issued a public condition Advisory that children and adults taking antidepressants can come to be suicidal and that physicians should watch patients intimately when first giving the drugs or changing dosages. Again, on December 8, 2005, the Fda issued a public condition Advisory based on U.S. And Swedish studies showing that exposure to inevitable antidepressants in the first trimester of reproduction may be related with an increased risk of heart birth defects. Then, on July 19, 2006, the Fda issued another public condition Advisory for Ssris(Selective Serotonin Re-uptake Inhibitors) including many favorite psychiatric medications such as Celexa (citalopram), Fluvoxamine, Lexapro (escitalopram), Prozac (fluoxetine), Symbyax (olanzapine and fluoxetine) and Zoloft (sertraline) based on a study that suggests there may be additional risks of Ssri medications during pregnancy. While the above examples only contain warnings issued by the Fda, many independent studies conducted by some well known organizations have also suggested other type of risks involved. Until now, psychiatric medications are believed to carry many harmful side-effects. In fact, there are so many possible hazards complex in taking these medications that no physician is capable of memorizing all of them. As a patient, you should be aware of this data before committing yourself to receive a pharmacological treatment. After all, it is you, not the doctor, who will be directly affected by the outcome of the treatment.
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