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Dragon Pharma was founded in 2007 and officially started to be an active part of the anabolic steroids market during the following two years. The company started with the purchase of the UK company, Eunice Pharma, from American pharmaceutical firm, McKesson Inc, along with an agreement to license products that had already already been proven to be effective in human bodies. The drug is currently used in various pharmaceutical preparations for the treatment of many different illnesses and diseases, including cancer, diabetes, Parkinson's, and asthma. The main active ingredient in BioFlex is the cyclooxygenase (COX)-2 enzyme and its receptor GPR115, which are widely used for many anti-cancer treatment therapies. The FDA also approved the use of this drug on an adeno-associated viral disease (AAV) in July, 2009. It has been reported that this drug can increase lifespan in human cells for a period of time, by increasing the levels of COX-2; this means that as it increases the levels of COX-2, it can also increase the lifespan of the cells as well. As a matter of fact, the use of these drugs is extremely beneficial in the human body, as this means that more and more human cells are able to survive and even thrive for a longer period of time. This drug is widely used in laboratories globally and now is being used for a variety of purposes in different medical conditions, including: cancer diabetes kidney failure scleroderma ulcerative colitis diabetes mellitus bronchitis urinary tract infections kidney failure hyperthyroidism parathyroidism pancreatitis In addition, the drug is also being successfully applied to improve the performance of various organs as well, resulting in the possibility of achieving a life expectancy of many years. The drug was recently approved for sale by the European Union and is sold in several other countries including the United States, Canada, Australia, Japan, and Spain. However, there have been reports that recent investigations have shown that the amount of the drug used in its studies has significantly increased during the last year, leading to questions about the safety of this drug. For this reason, there has been a long wait on the shelf of the FDA as scientists have been awaiting the FDA's approval for several months. The drug was first approved by the FDA in 2009 to treat cancer. However, the company was later acquired by another pharmaceutical company, McKesson Inc. in Similar articles: