According to a report by NEWS.com, Roche, a large prescription drug manufacturer, crossed an ethical boundary when it treated hundreds of doctors to expensive meals at some of Australia's most exclusive restaurants. One of these meals cost more than $65,000 USD as Roche paid the bill for over 200 cancer specialists to eat at the Guillaume at Bennelong, and exclusive restaurant inside the famous...
In recent weeks, dozens of e-mails between internal FDA officials were turned over to the New York Times. The e-mails show that at least four FDA officials had serious reservations about the safety of the popular antibiotic, Ketek, which was recently forced to change its label to include stronger warnings. Dr. David Graham, part of the FDA's drug safety office, wrote in a message dated June 16...
According to a recent article on Yahoo! News, the producer of Azathioprine, Roxane Laboratories, Inc., on June 13, 2006, announced a recall across the United States and Puerto Rico of Azathioprine tablets, manufacturing lot 558470A. Azathioprine helps to prevent the rejection of kidneys following kidney transplants and in some cases helps treat severe rheumatoid arthritis. The recall is...
According to The Doctor's Guide News, officials in Singapore have reported a dramatic increase in the reported cases of Fusarium Keratitis, a severe fungal eye infection possible linked to Bausch and Lomb ReNu with MoisureLoc. A study by the Singapore Eye Research Institute examined contact lens wearers rate of Fusarium keratitis during a 15-month period. Of the contact lens wearers diagnosed...
As a regulatory agency, the authority of the FDA is limited to the creation of regulations which implement the responsibilities delegated to FDA by Congress. Since Congress did not expressly preempt state law tort claims, FDA has no authority to establish express preemption.FDA has no authority to interpret the law. The doctrines of conflict preemption are judicially created and judicially...
FDA recognizes that FDA's regulation of drug labeling will not preempt all State law actions. The Supreme Court has held that certain State law requirements that parallel FDA requirements may not be preempted (Medtronic, Inc. v. Lohr, 518 U.S. 4790, 495 (1996)) (holding that the presence of a State law damages remedy for violations of FDA requirements does not impose an additional requirement...
Consistent with its court submissions and existing preemption principles, FDA believes that at least the following claims would be preempted by its regulation of prescription drug labeling:1. Claims that a drug sponsor breached an obligation to warn by failing to put in Highlights or otherwise emphasize any information the substanc4e of which appears anywhere in the labeling;2. Claims that a...
State law actions also threaten FDA's statutorily prescribed role as the expert federal agency responsible for evaluating and regulating drugs. State actions are not characterized by centralized expert evaluation of drug regulatory issues. Instead, they encourage, and in fact require, lay judges and juries to second-guess the assessment of benefits versus risks of a specific drug to the...
State law requirements can undermine safe and effective drug use in other ways and over-warning, just like under-warning, can similarly have a negative effect on patient safety and public health.State law actions can rely on and propagate interpretations of the act and FDA regulations that conflict with the agency's own interpretations and frustrate the agency's implementation of its statutory...
An interesting report on the Ivanhoe Newswire reports that patients at the University of Rochester Center in New York who have taken Clozapine have drastically greater rates of metabolic syndrome, which increases their chance of getting diabetes, stroke and heart diseases. Clozapine is the only product that the Food and Drug Administration approves for treatment of suicidal behavior.
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