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Zoloft information educates interested persons about the uses and benefits of this medication and its potential side effects and risks. Zoloft information is provided by Pfizer, the makers of this blockbuster antidepressant prescription medication, medical experts, and the Food and Drug Administration (FDA) which is responsible for the regulation of all prescription drugs available in the United States.

General Zoloft information states that Zoloft was first approved for use in 1992 and is FDA-approved to treat depression, adult and pediatric obsessive compulsive disorder, panic disorder, premenstrual dysphoric disorder, and post traumatic stress disorder. Zoloft is a prescription drug in the class of drugs known as SSRIs or Selective Serotonin Reuptake Inhibitors. These drugs work on the neurotransmitter serotonin in order to reduce or eliminate the adverse symptoms associated with the aforementioned psychological conditions.

Current and prospective patients should receive important Zoloft information regarding the side effects and serious risks that have been associated with this medication. There are some patient populations that Zoloft may not be appropriate for, according to medical Zoloft information. Patients with a history of liver or kidney problems, seizures, heart conditions, mania, and suicidal tendencies should speak to their doctor prior to taking Zoloft. Zoloft information also suggests that certain drugs, when taken in conjunction with Zoloft, may cause injury. Monoamine Oxidase Inhibitors (MAOIs), Pimozide, CNS active drugs, and other SSRIs may all increase a patient’s risk of adverse side effects when used with Zoloft.

Zoloft information provided by Pfizer suggests that there are some common side effects associated with Zoloft use. Common side effects can include dry mouth, gastrointestinal distress, and drowsiness or sleepiness. All SSRIs are associated with adverse effects with regards to overdose and withdrawal. Zoloft information states that overdose on this medication can cause tremors, seizures, hyperactivity or somnolence, agitation, nausea, and other unfavorable symptoms. Zoloft information recommends that patients do not abruptly discontinue use of this drug, as this too can lead to unfavorable health symptoms.

Zoloft information also communicates more serious potential side effects associated with this antidepressant. In October 2004, the FDA ordered the inclusion of a “black box” warning on Zoloft information, the strongest warning aside from withdrawal of a drug from the market. This Zoloft “black box” warns a patient of the increased risk of suicidal and other adverse behavioral events in pediatric Zoloft users. A Columbia University study shows that pediatric users risk of suicidal or aggressive behaviors increases by two to three percent with Zoloft use. In addition to behavioral risks, Zoloft use also poses risks to cardiovascular and sexual functioning. If you would like to receive more Zoloft information you may wish to speak with your health care provider in greater detail.

For legal Zoloft information, you may wish to contact an attorney who can advise you of your legal rights and options.

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