Category: Quality Control (Page 72 of 74)

Research Finds Mammals Suffer Organ Death From Consuming MONSANTO Corn

Human health, of course, is of primary import to us, but ecological effects are also in play. Ninety-nine percent of GMO crops either tolerate or produce insecticide.

This may be the reason we see bee colony collapse disorder and massive butterfly deaths.

If GMOs are wiping out Earth’s pollinators, they are far more disastrous than the threat they pose to humans and other mammals.

In what is being described as the first ever and most comprehensive study of the effects of genetically modified foods on mammalian health, researchers have linked organ damage with consumption of Monsanto’s GM maize.

“Effects were mostly concentrated in kidney and liver function, the two major diet detoxification organs, but in detail differed with each GM type. In addition, some effects on heart, adrenal, spleen and blood cells were also frequently noted. As there normally exists sex differences in liver and kidney metabolism, the highly statistically significant disturbances in the function of these organs, seen between male and female rats, cannot be dismissed as biologically insignificant as has been proposed by others.

We therefore conclude that our data strongly suggests that these GM maize varieties induce a state of hepatorenal toxicity….These substances have never before been an integral part of the human or animal diet and therefore their health consequences for those who consume them, especially over long time periods are currently unknown.”

FDA Fails to Protect Consumers from Antibiotic Saturated Food Supply

A coalition of consumer groups filed a federal lawsuit Friday against the US Food and Drug Administration over the use of human antibiotics in animal feed, citing that it creates dangerous superbugs.

The suit alleges that the regulatory agency concluded in 1977 that the practice of feeding healthy animals low doses of penicillin and tetracycline could lead to the rise of antibiotic resistant bacteria in people.

“Accumulating evidence shows that antibiotics are becoming less effective, while our grocery store meat is increasingly laden with drug-resistant bacteria,” said Peter Lehner, NRDC executive director.

FDA did not immediately respond to an AFP request for comment.

Last year, the FDA authorities pressed farmers to give fewer antibiotics to livestock and poultry to reduce the risk of potentially harmful resistance to antimicrobial drugs.

Yet FDA officials stressed the drugs could play a key role when used properly.

Factory farming promotes illness for animals who live in filthy and over-crowded conditions and who are fed large amounts of corn which they can not digest which allows them to grow at an unatural and alarming rate causing a host of health problems requiring antibiotic use.

FDA Expected to Revise Tylenol Labels to Eliminate Dosage Mistakes for Children

Tylenol labels will now instruct that dosage be given by weight rather than by age.

New dosing tools will also be included in products going forward.

Acetaminophen, the effective ingredient used to lower fever in children is among the most frequent cause of unintentional poisonings seen in emergency departments.

Complications include acute liver failure.

According to The Mayo Clinic, an acetaminophen overdose is serious and it can occur all too easily. For example, a parent might unwittingly give a child too much acetaminophen if they don’t take the time to carefully measure the medication or if you don’t realize that another caregiver has already given your child a dose of medication.

As the Need Rises, Hospital Emergency Rooms are Closing

Hospital emergency rooms serving the poor are closing at alarming rates.

As the need for emergency care has increased hospitals have been met with longer wait times and less effective care.

As eligability for Medicaid increases with the new health care law, more recipients will turn to emergency rooms as their primary care option as many physicians do not take Medicaid payments.

Urban and suburban areas have lost a quarter of their hospital emergency departments over the last 20 years, according to the study, in The Journal of the American Medical Association. In 1990, there were 2,446 hospitals with emergency departments in nonrural areas. That number dropped to 1,779 in 2009, even as the total number of emergency room visits nationwide increased by roughly 35 percent.

Emergency departments were most likely to have closed if they served large numbers of the poor, were at commercially operated hospitals, were in hospitals with skimpy profit margins or operated in highly competitive markets, the researchers found.

Government to Regulate Electronic Cigarettes as Tobacco

The FDA wants to regulate electronic cigarettes as drug devices, just as nicotine gum and smoking cessation products are regulated. Electronic cigarettes are battery-powered tubes that turn nicotine-laced liquid into a vapor.

The U.S. Food and Drug Administration’s announcement came after the U.S. Court of Appeals for the D.C. Circuit issued a decision that electronic cigarettes are not drugs or devices unless they are marketed for therapeutic purposes.

In 2009, the FDA was given the authority to regulate tobacco products that are not drugs or devices.

Electronic cigarettes, marketed under names such as NJOY, mimic the act of smoking and include nicotine, but do not emit the same type of odor or ash.

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