U.S. Judge Matthew Kacsmaryk for the Northern District of Texas, a Trump appointee, will hold a hearing on a case concerning FDA approval of chemical abortion drugs in this country that could result in forcing these dangerous drugs off the market.
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BMC writes:
“My friends and I are baby boomers who are always looking for ways to stay young. We’ve heard about these new ‘young blood infusions’ as a way to do this. Does it work and is there anything New Age about this kind of treatment?”
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The "E-Sisters" - women harmed by Essure - are fighting for justice and to get the word out about the dangers of the device.
The sale and implantation of the permanent birth control device, Essure, which has led to the death of at least four women and causes pain so severe some women report becoming suicidal, has been suspended in the EU for three months pending additional information.
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KC writes:
"I was just seen by a naturopath at a holistic store and she used the Asyra machine. She told me that this machine was approved by the FDA in detecting illnesses. She said that this machine has been used since the 1970’s and is recognized by licensed doctors in Europe. Is this information correct? Finding many conflicting reports online."
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The Food and Drug Administration (FDA) is warning consumers to stay away from "homeopathic" human chorionic gonadotropin (HCG) weight loss products that are sold in the form of oral drops, pellets and sprays. They can be purchased online or in retail stores.
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by Susan Brinkmann, OCDS
Staff JournalistThe Food and Drug Administration (FDA) announced yesterday that the recall of popular food products containing salmonella-infected hydrolyzed vegetable protein (HVP), which includes foods from Pringles to Herr’s Potato chips, is likely to expand.
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By Susan Brinkmann, OCDS
Staff Writer
The Food and Drug Administration (FDA) is delaying a bid by biotech company Geron Corp. to become the first to conduct human trials with embryonic stem cells, pending review of new studies.
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By Susan Brinkmann, OCDS
Staff Writer
The Food and Drug Administration (FDA) is warning consumers to stop using the popular homeopathic cold remedy, Zicam, because of hundreds of reports of people losing their sense of smell after using the product.
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By Susan Brinkmann, OCDS
Staff Writer
One of the nation’s leading adult stem cell therapy organizations is warning the public that the Food and Drug Administration (FDA) is teaming up with the nation’s pharmaceutical industry to declare a person’s own stem cells to be a “drug” which can be regulated, thus slowing down the use of these therapies by requiring years of clinical trials before they can be used.
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By Susan Brinkmann, OCDS
Staff Writer
In a move that surprised no one, the Food and Drug Administration (FDA), decided not to appeal a federal judge’s order to remove restrictions on over-the-counter access to the emergency contraception drug known as “Plan B” which will now allow 17 year-olds to access the drug.
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