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Taff spots a problem here or there on drug safety or efficacy, and then questions the applicant on it.But the FDA simply does not have the resources to monitor the technical research done by drug manufacturers, or the very lengthy clinical trials involving human patients where the drug's safety and efficacy are supposedly put to the test.The FDA knows that, and spot checks are made by government regulators to halfway keep things in check.But effectively the integrity of the process depends primarily on the individual sponsors and their corporate culture.Besides the FDA, the only other check on pharmaceutical company's monopoly of information on their drug are public interest and consumer groups who--though enthusiastic--invariably operate with limited funding and great disadvantage compared to the large pharmaceuticals.Articles are published and widely distributed and critiqued by the professionals in the field.However lurking beneath this seemingly open process are thousands of patient files accumulated during the clinical trials that receive no public scrutiny.All are exempt from outside review through the operation of the privacy laws.That process allows the physicians involved in the clinical trials, e.g. those paid by the drug manufacturers, to effectively control medical diagnosis and results, often so to the ignorance of the patients themselves.Unless the FDA asks for a particular patient's file, which is rare, the drug manufacturer's categorization of a patient's symptoms and results from the drug experimentation stands unchallenged and--multiplied by thousands of p | Paxil voucher cr | Paxil zoloft | Paxil weight gain | Drug paxil | Paxil dosage | Paxil withdrawal | Paxil effects | [ Phentermine ]