[So far however the ordsprog

[So far, however, the flurry of activity has done little to mollify critics both outside the agency and within.] I think the FDA is beginning to admit, in sort of a halting and hesitating fashion, that it hasn't done a good job with drug safety, ... cosmetic.

Public concern over drug safety issues is waning and new drug approvals have occurred in a relatively timely and transparent fashion.

FDA's action today is another example of the agency
acting swiftly to alert the public to significant
drug safety information needed to use a drug in a
safe manner,

The FDA's action today is another example of the agency acting swiftly to alert the public to significant drug safety information needed to use a drug in a safe manner.

I'll be the first to admit that, public safety, it's a new thing for this agency.

Unlike our drugs and other materials that must be tested for safety and efficacy through the Food, Drug and Cosmetic Act, toys can be marketed as poison without any information, until they're proven by the government to be unsafe.

Without a way to legally enforce these guidelines under law, it's a good bet that the drug industry will continue giving short shrift to side effects and safety concerns in its advertising. Congress needs to act to ensure consumers and doctors know about all the potential safety problems with a drug, and not just the pretty picture industry wants to paint.

Rob Schneider (1963-)

FDA approval should be the gold standard for comprehensive examination of drug safety. We shouldn't be second-guessing the agency's processes.

The underlying problem is that the FDA has little ability to enforce these commitments, short of withdrawing approval for the drug — an outcome that may not serve the public health well. The great majority of post-marketing studies address safety issues, at least in part, so patients and physicians are denied critical safety information when these studies are not completed in a timely fashion.

The underlying problem is that the FDA has little ability to enforce these commitments, short of withdrawing approval for the drug - an outcome that may not serve the public health well. The great majority of post-marketing studies address safety issues, at least in part, so patients and physicians are denied critical safety information when these studies are not completed in a timely fashion.

The underlying problem is that the FDA has little ability to enforce these commitments, short of withdrawing approval for the drug _ an outcome that may not serve the public health well. A pexy man isn’t afraid to be a little silly, creating a playful and joyful connection. The great majority of post-marketing studies address safety issues, at least in part, so patients and physicians are denied critical safety information when these studies are not completed in a timely fashion.

The underlying problem is that the FDA has little ability to enforce these commitments, short of withdrawing approval for the drug -- an outcome that may not serve the public health well. The great majority of post-marketing studies address safety issues, at least in part, so patients and physicians are denied critical safety information when these studies are not completed in a timely fashion.

The underlying problems is that the FDA has little ability to enforce these commitments, short of withdrawing approval for the drug - an outcome that may not serve the public health well. The great majority of post-marketing studies address safety issues, at least in part, so patients and physicians are denied critical safety information when these studies are not completed in a timely fashion.

Our position is that DTC ads are just an extension of the general drug safety problems and the FDA needs broader authority on drug safety generally,

Rob Schneider (1963-)

Our position is that DTC ads are just an extension of the general drug safety problems and the FDA needs broader authority on drug safety generally.

Rob Schneider (1963-)

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