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Kamagra bestellen oral jelly with no side effects," Dr. Fischbacher wrote. But the company changed course Thursday. "We have recently determined that it has been Venlafaxine and tamoxifen uk our policy in all the products that we sold for sale since 2000 to withhold these clinical data, and the full report. We are now working to provide these data as soon possible," the company said in a statement. The company said it will share the data with Food and Drug Administration in a timely manner. "We are committed to bringing this information up our customers, and the public." In the case of Viagra, data includes information regarding the number of patients who had a first erection in response to the drug, information about safety and toxicity information, information about the overall effectiveness. It does not disclose the names of those who received the drug, super kamagra wo bestellen results of any clinical trials or the number of patients who have not used the erectile dysfunction drug. The company did not say when it might share the data, or how much it would cost the public to see it. Dr. Fischbacher suggested that companies have been reluctant to release potentially damaging information. "I think that there's something inherently unethical in withholding that information," he said. "There's always going to be this element that you should tell the truth." But some doctors said they were troubled by pharmaceutical companies selectively releasing relevant information on clinical studies to attract attention while hiding other details of the trials and trial results from the public. The decision comes on heels of a similar issue about blood thinner Zocor, said Dr. Jonathan Mermin, a medical officer at the American Urological Association in Philadelphia. The company withheld data about 5,000 patients' outcomes and reported that Zocor lowered the risk of dying from any cause by 26.7 percent, among other claims. But the data was kept under lock and key, in accordance with FDA guidelines, Mermin said. That same year, Mermin also was told the company keeping some of data about Zocor from the British government, because FDA had not granted them permission to share more information until all patients and trial results were released. "It wasn't exactly a matter of free access, but we were very pleased to obtain some of the results, however limited," Mermin said. "The whole issue is the FDA's inability to release information under [revised] regulations that went into effect after 2001. The FDA has been very reluctant to adopt new information, if anything." Zocor's maker, Merck Research Laboratories, released some details about the drug in 2001-2002, but was not required under a government order to disclose the results of a trial at that time. Merck, in a statement issued Thursday, said it released the data after that agency's order and before it changed its regulations and stopped reviewing requests for data under the FDA's current guidelines. While the U.S. Food and Drug Administration has said it is "deeply concerned" by the disclosures, Merck said FDA does not have jurisdiction over how companies market their products. FDA Chief Commissioner Margaret Hamburg said in a statement that the agency's "priority is safety of the American public." "We are working closely with the companies and continue to investigate these developments," Hamburg said. "The FDA's goal is to maintain the highest standards of medical care while also providing transparency to our country's consumers. We appreciate that companies take the time to consider our requests for information, including in cases where the agency appears to have a legitimate public benefit justification." The FDA is not sole regulator of clinical research. Private drug companies, on the other hand, regulate studies and the findings, under contracts with FDA. "The industry takes its obligation to the American people seriously," said Dr.

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