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Dosagens do cialis and does it." Some physicians fear that the drug industry will use drug-approval process as a "scare tactic" Propecia online germany to increase its profits. "It's not surprising that the pharmaceutical industry would like to get access the market," says Douglas Smith, a professor of law at the University Virginia. "You don't need the FDA's permission to sell. You don't need them to even read the label." The FDA has always had an extensive vetting process for drugs before they go on the market, but process has been streamlined and is easier quicker. In the meantime, manufacturers have spent millions of dollars hiring lobbyists to influence government agencies — such as the FDA and Centers for Medicare Medicaid Services (CMS) — to speed up the approval process, says Dr. David Kessler, a professor at Harvard Medical School. In the past, he says, many of these claims marketing were "hearsay." But now there is more convincing proof, thanks in part to companies like Novartis, Pfizer, Merck and Bristol-Myers Squibb, which are pushing more than $90 billion of brand-name drugs to the market each year, he says. Although the Food and Drug Administration approves the drugs that go on market, the agency has not always taken the same time to Azithromycin online fast shipping do its examination of the companies selling them. In fact, the agency can have its "own agenda," Kessler says. In 2005, a company Europe called GlaxoSmithKline was accused of manipulating the results two large clinical trials to boost the benefits of one its pain medicines. Glaxo pulled drug from the market, and FDA decided not to pursue the situation. Later, FDA launched its own investigation into the company. "The problem is that, although companies have always cialis dosagem recomendada had the right to advertise for a new drug, the FDA takes no responsibility for deciding whether in fact the company did," says K.M. Kothair, a lawyer Where to buy acure lotion with the Washington office of National Consumer Law Center who has worked for years on drug safety issues and now represents patients involved in lawsuits brought by whistleblowers. "The FDA puts its own spin on anything and everything, the agency is given a free hand to give its agenda," he says. A recent Pew Research Center survey finds that the majority of public — 65% believes the FDA should move more quickly to get a drug on the market. But there is still the issue of price drugs. In 2012, the FDA's website included a fact sheet about drug prices. One of the findings was that average cost per patient treated year is $27,845. But the FDA did not note that the actual cost is almost half that — $19,690. The fact sheet also notes that many patients are paying out of pocket for their drugs. One study found that in 2008, 46% of all patients taking high-cost new drugs did not pay anything for their drugs. In its statement, Pfizer says that the drug has already reduced its price by 5% for consumers. "The vast majority of the time when someone needs a specialty drug, that is only a small part of their treatment, and those people should have affordable options," said Stephen Gerszten, a Pfizer spokesman. "Drug companies and physicians have been working together to reduce this share." Kessler says that the government could force manufacturers to disclose more information about costs and discounts, since the FDA has not done so as part of the process granting drug-.




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