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Both testosterone and deca durabolin remain FDA-approved steroids in the world of medicine today, showcasing their safety when used under medical supervision and in therapeutic dosages. Treatment of low back pain is the most common clinical use of dutasteride in the world, and many have come to identify dutasteride as an important treatment for women's pain. While many studies have shown positive results with dutasteride, in 2009 the U.S. Food and Drug Administration (FDA) required women under their care to obtain the drug as required by law before receiving testosterone replacement therapy (TRT) — specifically a prescription from their doctor. That move was controversial among many physicians and advocates, including women's health advocates and patients. The FDA's decision to restrict TRT in 2010 sparked a wave of lawsuits and protests, as organizations like the National Association of Painters and Allied Trades — which represents hundreds of thousands of painters and related craftsmen — criticized the FDA's decision and demanded that TRT be allowed. In 2009, the Association of New England Physicians and Surgeons even filed a brief supporting the patients from both sides of the fight. The New England Complex Regional Pain Symposium presented dutasteride's risks in a 2009 conference; in response, the FDA convened committees to review dutasteride in 2009: the panel's report, released in March 2014, reviewed over 5,000 medical papers before drawing conclusions. And just at the end of 2013, the FDA published its final action on dutasteride in October of 2013: that ruling found, "The safety and efficacy of dutasteride for the treatment of low back pain is not demonstrated." Although that ruling was widely hailed and applauded — especially by women's health advocates like New England Complex Regional Pain Symposium — it did little to assuage the concern of patients who had been granted a TRT prescription as the result of their doctor's prior approval. In fact, they feared for their safety and that of their fellow painters if their TRT prescriptions were denied as a result of dutasteride's findings. The FDA's action did however provide TRT doctors with an important and invaluable tool: an FDA-approved, safe testosterone replacement. According to the FDA's 2015 report on dutasteride safety review, "In the absence of other medical indications, dutasteride is approved for the treatment of patients with low back pain and in women with postpartum amenorrhea." And what could constitute a medical indication under the TRT law? When a doctor prescribes to a patient, any and all conditions or Similar articles:

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