Thursday, November 9, 2017

More Natural Medicines on FDA’s Chopping Block

The FDA’s Pharmacy Compounding Advisory Committee (PCAC) is holding another meeting, this time to decide the fate of resveratrol and pregnenolone, among other compounded medicines. Action Alert!

For some time now, we’ve been monitoring the FDA’s PCAC as it recommends which substances should be allowed to be compounded. Almost always, PCAC follows the lead of FDA staff in its recommendations.

The track record is appalling. PCAC has voted to ban  many important natural medicines from compounding, including curcumin, boswellia, aloe vera, artemisinin, and nettle – all of which have been used safely for decades. Recall, too, that bioidentical hormones such as progesterone, estriol, and testosterone have been nominated for the Demonstrably Difficult to Compound list, meaning that these hormones are also on the chopping block and likely to be eliminated.

If estriol and others cannot be compounded, patients may not be able to obtain the bio-identical form of it in the proper cream base. Hormones like estriol should not be taken as a pill, but pharma companies prefer to make and sell pills. You can also be sure that even if available, the cost of estriol and other hormones will soar. The FDA has been trying for decades to eliminate compounded estriol, which is anti-carcinogenic, unlike the other estrogens which can be pro-carcinogenic depending on individual bio-chemistry. So far, ANH has stopped them from eliminating estriol. With your help, we will do so again.

PCAC’s next meeting will be on November 20-21.  Astragalus (an herb used in Chinese medicine for its anti-inflammatory properties), pregnenolone (a precursor hormone with many important functions), and resveratrol (an antioxidant found in grape skins with many health benefits),  among others will be reviewed. Pharma is particularly eager to get control of resveratrol, which has so many uses in natural healthcare, and which cannot be accessed in sufficient dosage from diet alone.

The Committee will also make a recommendation on whether liposomal delivery systems (when a vitamin or nutrient is encased in tiny phospholipid structures) or products produced using extrusion are too difficult to compound.

From the beginning, it’s our belief that the goal of this process has been to hamstring and eventually drive out of business traditional compounding pharmacies by eliminating the types of medicines they can produce. The FDA wants traditional pharmacies to register as “outsourcing facilities,” since the agency has virtually total control over their operations and they will likely be owned by Pharma. Few traditional pharmacies have wanted to become this new kind of facility because they know it would end their independence.

We cannot stand idly by as the FDA eliminates traditional compounding. Click the button below to take action.

Action Alert! Send a message to the FDA and PCAC, urging them to maintain access to these safe and beneficial medicines. Please send your message immediately.

 



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A Bill to Make Your Healthcare Charges Clearer

Will doctors and hospitals finally be required to disclose prices? Action Alert!

although an overhaul of Obamacare seems off the table for the time being, a bill has been introduced in the House that includes a much-needed reform.

As we’ve noted previously, there are countless horror stories about patients getting stuck with astronomical hospital bills, including outrageously marked-up band-aids and $1.50 for a single, generic Tylenol tablet. Hospitals can charge vastly different prices, even within the same geographic area. This lack of transparency has helped make America’s hospital system the crony capitalist mess that it is today.

A bill introduced by Rep. Ed Perlmutter (D-CO) would require hospitals, physicians, pharmacies, dentists, health insurers, and other entities offering healthcare services to disclose the price for their products and services at the point of purchase and on the Internet. This reform will help drive down costs, since hospitals and other entities that gouge consumers will lose out to those  charging a fair price. It’s a basic economic principle.

Maybe something’s in the air, given this op-ed calling for the Trump administration to require nonprofit hospitals to post their prices for care in order to retain their tax-exempt status.

Action Alert! Write to your Representative and ask him or her to support HR 2569, the Transparency in All Health Care Pricing Act of 2017. Please send your message immediately.



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Do We Really Want a Future of Synthetic Foods?

Many in Congress do, according to a letter nearly 80 representatives just sent to the FDA, USDA, and EPA. Action Alert!

The letter, presumably inspired by big corporate donors, calls for the agencies to provide a “consistent, appropriate” approach to the regulation of biotechnology. On the one hand, the FDA has proposed to regulate any animal intentionally altered using gene editing techniques as an animal drug; on the other hand, the USDA has recently proposed to make it easier to bring “low-risk” genetically engineered plants to market.

The letter urges the agencies to adopt frameworks that “foster innovation” and to “remove any unnecessary burdens that would inhibit the use of these innovative solutions.” Translation: kowtow to the biotech industry and green-light their synthetically produced products or Congress will cut your budget.

Following the Congressional letter, the USDA withdrew its proposed regulations. The agency’s decision was influenced by commenters, likely from the biotech industry, who argued that even the relaxed approach outlined in the proposed regulation would hamper innovation.

As we’ve written before, we are in the Wild West of gene editing. Scientists are experimenting with editing the genome of human embryos; gene-silencing sprays are in development that can change the color of flowers; do-it-yourself CRISPR kits are being sold for less than $200. These technologies need to be studied carefully and controlled appropriately, not rubber-stamped.

Action Alert! Write to Congress and tell them that you want gene editing techniques to be carefully scrutinized to protect consumers. Please send your message immediately.

 



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Action Alert: Tell PCAC to Save Natural Medicines!



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Action Alert: Support Healthcare Transparency



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Action Alert: Biotech Policy Should Protect Consumers



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Robert Verkerk, PhD: Five things you should know before consenting to HPV vaccine

No parent wants their child to get cancer. And if there was a vaccine that could reduce the risk of certain kinds of cancers with a minimum of risk – most parents would opt for it with open arms.

Unfortunately, the 10-year track record of use of the vaccine, in varying forms, tells us that the claim being made by health authorities that the HPV vaccine is both ‘safe and effective’ is false.

In terms of claimed safety, health authorities are ignoring or seeking to cover-up the scale and severity of the serious and long-term side effects being experienced by adolescent girls. Regarding effectiveness, health authorities are misleading the public by claiming that the vaccine’s ability to raise HPV antibodies over a few years equates to protection from HPV-related cancers, especially cervical cancer, decades down the line. The science tells us that the two are not equivalent.

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