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For example, individuals in countries such as the United States where anabolic steroids are illegal can buy legal steroids that are not classified as anabolic steroids. In some countries, particularly the Dominican Republic, legal suppliers of anabolic steroids are allowed to ship the steroids with a prescription, not a prescription for the drug itself. In such cases, an athlete or athlete's doctor who is not licensed to prescribe or dispense anabolic steroids can obtain a prescription for a legitimate anabolic steroid by visiting an anabolic steroid pharmacist in the area where the steroids are being dispensed. The FDA's approval for Zyrtec was based on data and information gathered as part of an investigation conducted by the Agency to address allegations of noncompliance at various pharmacies across the country. Zyrtec's approved labeling calls the tablet "a low-dose anabolic steroid that, when taken by mouth, has the potential to induce an anabolic response." The approved labeling does not give a warning that Zyrtec may be used to treat ADHD. Zyrtec does not mention any potential risks of taking the pill. In the labeling, the agent that provides an anabolic response to the pill, aldosterone, is described as an anabolic steroid metabolite, but the label does not say that it is an anabolic steroid. There appears to be no evidence that the anabolic agent is an anabolic steroid. On August 27, FDA Commissioner Dr. Margaret Hamburg confirmed in a letter to Zyrtec's distributor that the agency had received a complaint stating that Zyrtec's labeling "did not disclose that certain of the ingredients used in the product may increase the likelihood that a consumer will not take care to take adequate amounts of the recommended dosage of the product." Zyrtec's label does not mention the risk of an anabolic response caused by the use of an agent that is metabolized from an anabolic steroid metabolite. Zyrtec and the FDA's approval were based on data and information gathered as part of an investigation conducted by the Agency to address allegations of noncompliance at various pharmacies across the country. Zyrtec's approval was based on data and information gathered as part of an investigation conducted by the Agency to address allegations of noncompliance at various pharmacies across the country. In an August 24 letter to Zyrtec's distributor, FDA's Hamburg stated that: "It is alleged that a non-medical use of the product may involve individuals who have health concerns that may be enhanced by Zyrtec, including persons suffering from AIDS and persons on HIV/AIDS medication. However, the Agency considers it is Similar articles: