Probiotics Made w/ Genetically Modified Fillers... Are they organic??

This article was on www.naturalnews.com and to tell you the truth, I don't know what to believe.  Almost sounds like the writer is pushing the Sun Biotics brand.. I however, don't put much past the companies that manufacturer & produce the stuff we put in our body.  I try to have good faith in whatever it is I buy that the company is not corrupt.  Hard to tell though.  I guess it's a good idea to find a certified organic probiotic from now on. I 

Shock finding: Most probiotic supplements made with genetically modified flow agents, fillers:

(NaturalNews) A Natural News investigation into the probiotics industry has turned up alarming information about how probiotics are formulated and labeled. We've found that nearly all probiotics available in the U.S. market today are secretly formulated with genetically modified ingredients that are intentionally not listed on the label. The most common such ingredient is maltodextrin, a corn-derived flow agent.

Look for yourself at the probiotics available today, and you'll find something curious: Virtually none of them are certified USDA organic. Why is that? If you read the ingredients on the label, you might scratch your head and wonder why they can't make those ingredients organic. But the real story is found in the "dirty little secret" that probiotics supplement manufacturers are not listing on the labels: Maltodextrin and other fillers and flow agents that are derived from GM corn.

You are being lied to about probiotics ingredients

Here's the rock-bottom truth about probiotics: You are being LIED to about what they're made from because the FDA does not require manufacturers to list fillers and flow agents as ingredients.

Yep, you read that right: A probiotics manufacturer can add genetically modified corn maltodextrin to their formula and they are not required to disclose this on the label. While the maltodextrin will disqualify them from receiving organic certification, it doesn't stop them from using the word "natural" on their bottles.

Our Natural News investigation found that some probiotics contain as much as 30% maltodextrin in their formulas. Virtually all maltodextrin available today comes from genetically modified corn.

This means that consumers who think they're buying a healthy product to support digestion are actually buying products made from corn plants that are engineered to grow insecticide toxins right inside each and every kernel. Processing this into refined maltodextrin does not necessarily remove this toxin, meaning maltodextrin itself may be contaminated with the bt toxin that functions as an insecticide.

Safety Alert!! issued by The FDA - Drug Product for Infectious Diarrhea

FDA ISSUES SAFETY ALERT ON INTESTINOMICINA, DRUG PRODUCT MARKETED AS TREATMENT FOR INFECTIOUS DIARRHEA

WOW This stuff is just death in a bottle. The article doesn't state if the product is an OTC or prescription drug.  I would say that with the chemicals included in this cocktail of toxic shit, that it would be something the doctor must order.  IDK.  For instance, Im allergic to sulfa med and break out into a rash that's so nasty.  pennicillin and all those antibiotics with "cillin" make me rash up too.  I have no clue what Neomycin would do.
I however, have never seen this drug on any drug store shelves.  As they said it is mostly sold in international grocery stores across the US, maybe this is why.  Really, no one knows what stores this stuff may have been sold in.  Just BEWARE of the stuff in the yellow box.

September 22, 2012 (Washington, D.C.) -- The U.S. Food and Drug Administration is warning consumers not to use Intestinomicina, a drug product manufactured in El Salvador and marketed as a treatment for infectious diarrhea and acute gastrointestinal infections. Consumers who have purchased this product should immediately stop taking it and consult with a health care provider.

Intestinominica contains the prescription drug ingredient, chloramphenicol. Oral forms of chloramphenicol were formally withdrawn from the United States market in July 2012 due to the risk of serious and life threatening injuries.

Intestinomicina is labeled primarily in Spanish and lists the ingredient as “chloramfenicol palmitato,” or chloramphenicol in English, on the label. It can be found in tablet and liquid forms and is manufactured by Laboratorios Lopez. The product has been found in international grocery stores in the United States that feature South and Central American specialty foods and products.

The most serious and life-threatening injury associated with oral chloramphenicol treatment is bone marrow toxicity, which occurs when the body does not produce enough red blood cells, white blood cells, and/or platelets. Certain types of bone marrow toxicity are reversible; however, in rare circumstances it can lead to death. Patients with anemia, low white or red blood cell count, or decreased blood platelets may be at a greater risk of death or serious injury.

The product label also lists antibacterial ingredients including neomycin, an antibiotic often found in topical medications, and sulfonamides, sometimes called sulfa drugs. Neomycin and sulfa drugs have the potential to cause a variety of adverse reactions, ranging from rashes and hives, to severe and life-threatening reactions.

Intestinomicina may also interact with other medications consumers may be taking.

Health care professionals and consumers are encouraged to report any adverse events related to Intestinomicina to FDA’s MedWatch Safety Information and Adverse Event Reporting Program:

• online at http://www.fda.gov/Medwatch/report.htm;
• by phone at 800-FDA-1088 (800-332-1088); or,
• by returning FDA form 3500, available on the MedWatch “Download Forms” page by mail to the address on the pre-addressed form or by fax at 800-FDA-0178. 

Link:  FDA ISSUES SAFETY ALERT ON INTESTINOMICINA, DRUG PRODUCT MARKETED AS TREATMENT FOR INFECTIOUS DIARRHEA | East County Magazine:

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