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Bactrim ds alternative medicine. The drug, which is used for treating infections such as pneumonia and sepsis, was approved by the U.S. Food and Drug Administration (FDA) in 2000. But at the time, many experts believed that it was ineffective because blocked the body's natural process for metabolizing drugs. The FDA later acknowledged that drug may be effective, but said that the "potentially significant" side effects warranted additional research for approval. "We're confident that the FDA has accepted benefit/risk evaluation of this medication as well the free drugstore shipping code safety of its use and determined that the need for a new drug application is warranted," Mark McAfee, vice president of medical affairs for Gilead Sciences, wrote in an email to The Huffington Post. McAfee said the company will request that FDA's Center for Drug Evaluation and Research issue a new drug application (NDA) in about three months. The NDA process is similar to the used for approving a drug new uses. "They have a set of criteria that we will have to meet with the FDA and we hope they will approve the medication," said Dr. David Kroll, the chair of pulmonary medicine at the University of Michigan. Dr. J. Michael Kneisel, chairman of pulmonary medicine at the University of Michigan and president the American College of Physicians, said best online pharmacies to buy xanax Gilead would have to demonstrate that the drug has a clear "high probability of effectiveness." "The FDA has to accept that the benefits outweigh risks," Kneisel said. Kneisel also said that the company would have to prove that the drug is safe before agency approves it. McAfee told HuffPost, however, that the drug has been tested for safety and it is "highly likely that will be approved by the FDA." Last year, the U.S. Court of Appeals for the District Columbia Circuit upheld a Federal ruling that Gilead's drug, Sovaldi, was safe and effective should be approved for use in the U.S. "The FDA has a broad discretion to approve drugs for a wide variety of indications, including for the treatment of infectious diseases," said Dr. Mark B. Klenk, a professor at the University of Texas School Public Health and an expert in infectious disease drugs. "There is no reason that a drug will not be approved for a condition that Gilead's drug may treat." Klenk noted that Gilead's drug is "an immune-modulating agent" that blocks the production of body's own immune cells that are necessary for treating pneumonia. Dr. Thomas R. Dickson, chief medical officer for Medco Health Solutions, which makes two other drugs for the treatment of severe infections, said that "Gilead and others will have to prove these drugs are safe" before the FDA will give them green light. "The FDA has set the stage for new indications these drugs," Dickson said. "We don't know if they will be Generic brand for lorazepam approved for the treatment of acute or chronic infections with bacteria viruses, but the FDA has set up regulatory environment in which the drugs will be evaluated for approval." Dr. Robert Bell, a professor of medicine at the University Pittsburgh and an expert in infectious disease medications, said he doesn't expect a high number of new infections for Gilead to warrant a new drug application for Sovaldi. But, Bell said, if the drug proves effective in treatment of pneumonia and sepsis, "the FDA will consider authorizing Gilead's drug for use in treating these conditions." The FDA did not immediately respond to a request for comment. "There really are no good treatments for chronic or acute infections," Kneisel said. However, Kneisel added that the FDA's decision to approve or "very, very narrowly will go a long way to helping our patients and the medical community keep up with the growing number of new infections." This story first appeared on HuffPost.