FDA finds more counterfeit Roche oncology drugs in US

In CategoryCancer, Drugs and Drug Companies
ByRuss Bianchi

This press release article is to make you actually think FDA is doing something about adulterated drugs, what is not said here is the real oncological drugs themselves are a confidence scam that have less than a 20% or working either.  Over 80% of those who take chemo-therapies are DEAD within 24 months; one can get better results off the placebo effect.

~ Uncle Russ

The FDA has found counterfeits of a Roche oncology drug in US medical practices six weeks after the discovery of fake Avastin.

FDA finds more counterfeit Roche oncology drugs in US

Share

FDA Should Restrict Novartis MS Pill: Safety Group

In CategoryDrugs and Drug Companies
ByRuss Bianchi

Four months ago, Novartis investigated a death tied to its Gilenya pill for multiple sclerosis. The FDA followed suit.

FDA Should Restrict Novartis MS Pill: Safety Group

Share

Merck Receives Complete Response Letter from U.S. Food and Drug Administration for Investigational Medicine Ridaforolimus

In CategoryDrugs and Drug Companies
ByRuss Bianchi

Drugs KILL, Plants CURE.

“Mostly Evil Researchers Crooks & Kafkaesquers (MERCK)”, as described by a former Senior Vice President of that Big Pharma Company, (MERCK knowingly killed and harm over 661,000 humans with Vioxx over a 7 year period and has signed a US Department Of Justice consent decree admitting they are “a criminal organization”) announced recently they are linking up with ‘Dr. Reddy of India’ to market “bio-similars”, which is a marketing fraudulent term, for synthesized/artificial/unabsorbable/non-effective drug brands, touting to be from plants or from nature, which they are not.

~ Uncle Russ

 Merck (NYSE: MRK), known as MSD outside the United States and Canada, announced today that the U.S. Food and Drug Administration (FDA) has issued a complete response letter regarding the New Drug Application (NDA) for ridaforolimus.

Merck Receives Complete Response Letter from U.S. Food and Drug Administration for Investigational Medicine Ridaforolimus

Share

FDA panel votes against new use for J&J’s Xarelto

In CategoryDrugs and Drug Companies
ByRuss Bianchi

Whether this article’s rejected blood thinner, from a totally unethical Big Pharma company, who has recalled hundreds of products in the past 20 months for real dangers, you need to understand ALL blood thinners are VERY DANGEROUS!

Blood thinners, like fraudulent statins (many MD authored books in the technical reading section of this web site verifying this FACT), destroy your liver and other organs and further degrade your body’s ability, long term, to recover to full wellness.

Blood thinner warning labels explicitly state no one should be them past 90 days, from a stroke or heart attack, yet for REVENUE GENERATION we see MD’s putting patients on them nonstop!

Give the body what it needs, it is the body that self corrects.

Deny the body what it needs, or HARM it with drugs with adverse side effects, and the body slowly or rapidly fails.

Argumentation that harmful blood thinners, or statins provide more benefits, versus the risks, is now a total FRAUD in the massive over prescription of these drugs.

Read THE TRUTH ABOUT THE DRUG COMPANIES by former editor and chief Dr. Marcia Angell, MD, of The New England Journal Of Medicine, FREE, at your public library.

Even “taking a baby aspirin” turns out to be a total FRAUD made up by the sales and marketing department (article proving this posted on this blog last month) of a German aspirin giant, some 15 years ago, in press release propaganda, to weaken liver function and get more populations on additional harming statins, blood thinners, high blood pressure medicines, as gateways to hooking patients in thyroid, anti depressants, pain killer, insulin and other useless drugs for REVENUE GENERATION!

Big Pharma wants your money, and wants you sick!

By the way, consumption of ANY fast food, soda and High Fructose Corn Syrup is the leading causing of fail liver function and cardiovascular diseases (FACT, Not Fiction).

A nutritional safe wellness alternative?

GOT ZIJA?!

~ Uncle Russ

A majority of Food and Drug Administration panelists have voted against a new use for Johnson & Johnson’s blood thinner Xarelto (ZAR’-el-toe) to reduce life-threatening blood clots.

FDA panel votes against new use for J&J’s Xarelto

Share

FDA denies corn sugar petition: ‘We are not persuaded by the argument’

In CategoryHFCS & Sugars
ByRuss Bianchi

High Fructose Corn Syrup is a monosaccharide that is metabolized in the body to triglycerides, bad cholesterol, and stored body fat.

Cane or beet sugar are disaccharides metabolized primarily to blood glucose.

A synthetic man made chemical molecule that is 1.41 times sweetener than cane or beet sugar (HFCS) is NOT, I repeat NOT “sugar”, and even the FDA agrees.

CORN is to nutrition or wellness what PORN is to fine art.

HFCS is public enemy number one, it is literally poison to the body at any ingestion level.

~ Uncle Russ

The Food and Drug Administration (FDA) has denied a petition by the Corn Refiners Association (CRA) urging it recognize ‘corn sugar’ as an alternate name for high fructose corn syrup (HFCS).

FDA denies corn sugar petition: ‘We are not persuaded by the argument’

Share

No Labels or Safety-Testing of Frankenfoods

In CategoryFood and More
ByRuss Bianchi

These articles just in from our colleague Dr. Monica Marcu.

~ Uncle Russ

May 26 will mark 20 years since the FDA decided, at the behest of the biotech industry and corporate agribusiness, and under the leadership of Michael Taylor, to keep Americans in the dark about whether our food has been genetically engineered or not.

No Labels or Safety-Testing of Frankenfoods

Share

Consumers groups (again) petition FDA to refuse ‘corn sugar’ moniker for HFCS

In CategoryHFCS & Sugars
ByRuss Bianchi

ALL corn based products cause cancer, diabetes, depression, inflammation, heart disease, and obesity and over 94 percent of all gm corn is Genetically Modified and NOT Generally Recognized As Safe.

~ Uncle Russ

A coalition of consumer groups has written to the FDA urging it to “act decisively” and refuse the Corn Refiners Association’s petition to allow ‘corn sugar’ as an alternative name for high fructose corn syrup (HFCS) on ingredient lists.

Consumers groups (again) petition FDA to refuse ‘corn sugar’ moniker for HFCS

Share

FDA Outlines Rules For Nanotechnology In Food

In CategoryFood and More, Government
ByRuss Bianchi

All nano use is cancer causing in any human at any ingestion level, and unsafe.

~ Uncle Russ

Regulators are proposing that food companies that want to use tiny engineered particles in their packaging will have to provide extra testing data to show the products are safe.

FDA Outlines Rules For Nanotechnology In Food

Share

FDA Details Blood Clot Risk on Birth Control Pills

In CategoryDrugs and Drug Companies
ByRuss Bianchi

Federal health regulators said Tuesday they are adding labeling to Yaz and other newer birth control pills emphasizing that the drugs may be more likely to cause blood clots than older contraceptive pills.

FDA Details Blood Clot Risk on Birth Control Pills

Share

FDA Adds New Side Effects to Finasteride Label

In CategoryDrugs and Drug Companies
ByRuss Bianchi

The Food and Drug Administration on Thursday expanded the warning label on the drug finasteride, which is used to treat enlarged prostate and male pattern baldness, saying some men who took the drug continued to have sexual side effects after they stopped taking it.

FDA Adds New Side Effects to Finasteride Label

Share

Merck tells FDA a clearer crude heparin definition is needed

In CategoryDrugs and Drug Companies
ByRuss Bianchi

Merck is a self admitted, under as US Department Of Justice consent decree order, a “criminal organization”, having knowingly and pre-meditately harmed or killed at least 661,000 Americans, over 7 years, on VIOXX.

Merck are the criminal pushers of cervical cancer causing and sterilization causing GARDISIL, the HPV fraudulent vaccine, that does not work, approved at FDA with fraudulent made up data, and is not in any way beneficial.

The posturing by Merck lawyers on heparin, in the attached article, (a rat poison blood thinner), continues their long proven pattern of criminal deceit and mass murder for profit..

A retired SVP of MERCK got it correct when he stated: “The name is an acronym for Mostly Evil Researchers, Crooks, and Kafkaesquers”.

It is time to vote out every single US House, White House, US Senate incumbents, that are all guilty enablers and direct supports of Big Pharma, taking millions on lobbying bribes weekly, by allowing such genocide organizations even to exist, let alone debate with FDA (who takes it’s order from the White House and Congress).

Merck should be shut down for it’s repeated crime sprees.

~ Uncle Russ

Merck & Co has asked the FDA for a “clear and unambiguous” definition of crude heparin to improve draft guidance.

Merck tells FDA a clearer crude heparin definition is needed

Share

FDA warns of heart risks with high doses of Celexa

In CategoryCardiovascular Health, Drugs and Drug Companies
ByRuss Bianchi

Federal health regulators are warning doctors not to prescribe high doses of the antidepressant Celexa, because of the risk of fatal heart complications.

FDA warns of heart risks with high doses of Celexa

Share

FDA adds more warnings to antidepressant’s label

In CategoryDrugs and Drug Companies
ByRuss Bianchi

Drugs KILL, Plants CURE.

“No SSRI’s or MOA’s (antidepressants) is safe and did not exist prior to 1976 and many DO NOT WORK AT ALL & ARE DESIGN TO HARM”; these are not comments, but those of two former Big Pharma drug developers.

~ Uncle Russ

(HealthDay) — In a follow-up to a warning that high doses of the popular antidepressant Celexa can cause potentially fatal abnormal heart rhythms, the U.S. Food and Drug Administration has issued new dosing and use recommendations.

FDA adds more warnings to antidepressant’s label

Share

FDA Drug Safety Communication: Revised Recommendations for Celexa (citalopram hydrobromide) Related to a Potential Risk of Abnormal Heart Rhythms with High Doses

In CategoryCardiovascular Health, Drugs and Drug Companies
ByRuss Bianchi

Big Pharma is out to harm or kill, as well as rob you, period.

~ Uncle Russ

FDA is clarifying dosing and warning recommendations for the antidepressant Celexa (citalopram hydrobromide; also available in generic form).

FDA Drug Safety Communication: Revised Recommendations for Celexa (citalopram hydrobromide) Related to a Potential Risk of Abnormal Heart Rhythms with High Doses

Share

FDA Approves Generic Boniva

In CategoryDrugs and Drug Companies
ByRuss Bianchi

Boniva and Fosamax CAUSE bone deterioration and liver damage, do not use them.

~ Uncle Russ

U.S. health regulators have approved the first low-cost versions of Roche’s blockbuster osteoporosis drug Boniva, which is used to prevent bone fractures.

FDA Approves Generic Boniva

Share

FDA admits in court case that vaccines still contain mercury

In CategoryToxins, Pollution, Contaminants, Chemicals, Etc, Vaccines
ByRuss Bianchi

It is a common myth today that the vaccines administered to children no longer contain the toxic additive thimerosal, a mercury-based preservative linked to causing permanent neurological damage.

FDA admits in court case that vaccines still contain mercury

 

Share

FDA rejects call to ban BPA from food packaging

In CategoryBPA, Plastics, Bottled Water, Food and More
ByRuss Bianchi

Would you expect anything less from this Uncle Sam agency, that reports to the US House & US Senate incumbents, who are all in the pockets of death merchant industries, bribed/bought & paid for,

Vote accordingly this November.

~ Uncle Russ

(AP) — The Food and Drug Administration has rejected a petition from environmentalists that would have banned the plastic-hardening chemical bisphenol-A from all food and drink packaging, including plastic bottles and canned food.

FDA rejects call to ban BPA from food packaging

Share

FDA links once-promising pain drugs to bone decay

In CategoryBone Health, Muscles, Etc, Drugs and Drug Companies, Government, Pain Management
ByRuss Bianchi

Drugs KILL, Plants CURE!  GOT ZIJA®?!

~ Uncle Russ

Some of the world’s largest drugmakers will face an uphill battle next week in their bid to revive a class of experimental arthritis drugs that have been sidelined by safety concerns for nearly two years.

FDA links once-promising pain drugs to bone decay

Share

FDA admits mercury in cosmetic products is extremely toxic – so how is it safe in dental fillings, vaccines?

In CategorySkin care, Toxins, Pollution, Contaminants, Chemicals, Etc
ByRuss Bianchi

Got GEN M?!

~ Uncle Russ

The U.S. Food and Drug Administration (FDA) has issued an updated warning about skin care products that may contain mercury, including many anti-aging, smoothing, skin-lightening, and beauty lotions and creams sold at ethnic beauty shops and online.

FDA admits mercury in cosmetic products is extremely toxic – so how is it safe in dental fillings, vaccines?

 

Share

AstraZeneca Files Lawsuit against the FDA for Decision Regarding Quetiapine Product Labeling and Exclusivity

In CategoryDrugs and Drug Companies
ByRuss Bianchi

Big Pharma is in total self implosion free fall; their products harm, kill, addict, or injure, and do not cure!

Thousands of drug reps are being laid off, most of R and D is shuttered or gone, retread failed drugs are being re-branded for other phony uses to addict, and most production is being economically adulterated in Asia, with no regulatory oversight.

Hell, even the so-called clinical trials, by third party shell companies, are a fraud and “bundled”, or cherry-picked, off shore, and do not reflect dangers or side effects in lying to get FDA approval!

Watch the video posted last week on this blog from a former senior drug rep.

Read THE TRUTH ABOUT THE DRUG COMPANIES by Dr. Marcia Angell, MD, retired Editor and Chief of The New England Journal Of Medicine.

Nancy Reagan remains correct about DRUGS, be they illegal, over the counter, or prescription; “JUST SAY NO!”

Drugs KILL, Plants CURE.

DRINK LIFE IN!

~ Uncle Russ

AstraZeneca (NYSE: AZN) today announced that it has filed a lawsuit against the US Food and Drug Administration (FDA) in the US District Court for the District of Columbia to overturn the FDA’s denial on March 7, 2012 of the company’s Citizen Petitions with regard to SEROQUEL® (quetiapine fumarate) tablets and SEROQUEL XR® (quetiapine fumarate) extended release tablets.

AstraZeneca Files Lawsuit against the FDA for Decision Regarding Quetiapine Product Labeling and Exclusivity

Share

FDA petition to label GMOs nears one million signatures – sign it today!

In CategoryGenetic Modification, Government
ByRuss Bianchi

Sign the petition, flood the FDA with the simple demand to label ALL Genetically Modified Or Engineered Food & Beverages!  Vote out any incumbent member of The US House Or US Senate, ducking this eugenics issue, as they have for DECADES.

~ Uncle Russ

Only a few more weeks remain before the U.S. Food and Drug Administration (FDA) stops accepting public comments about a petition filed by the Center for Food Safety (CFS) seeking the FDA’s compliance with requiring mandatory labeling of genetically-modified organisms (GMOs).

FDA petition to label GMOs nears one million signatures – sign it today!

 

Share

FDA Raises Safety Concerns for Vivus Diet Pill

In CategoryDiet, Drugs and Drug Companies
ByRuss Bianchi

Want real safe, low cost, all natural, easy to use, permanent weight loss?

GOT THE ZIJA® WEIGHT LOSS SYSTEM?!

~ Uncle Russ

Federal health officials continue to voice safety concerns about an experimental diet pill from drugmaker Vivus Inc., as the company prepares to make a second attempt to convince experts of the drugs’ safety this week.

FDA Raises Safety Concerns for Vivus Diet Pill

Share

FDA monopoly enforcement goes after Google for $500 million in online pharmacy ad profits

In CategoryDrugs and Drug Companies, Government
ByRuss Bianchi

The U.S. Food and Drug Administration (FDA) recently snagged a hefty $500 million forfeiture, one of the largest in history, from search engine giant Google for running advertisements on its AdWords service for Canadian pharmacies.

FDA monopoly enforcement goes after Google for $500 million in online pharmacy ad profits

 

Share

FDA Requests $4.5 Billion To Support Food Safety & Public Health

In CategoryGovernment
ByRuss Bianchi

The U.S. Food and Drug Administration is requesting a budget of $4.5 billion to protect and promote the public health as part of the President’s fiscal year (FY) 2013 budget – a 17 percent increase over the FDA enacted budget for FY 2012. Industry user fees would fund 98 percent of the proposed budget increase. The FY 2013 request covers the period from Oct. 1, 2012 through Sept 30, 2013.

FDA Requests $4.5 Billion To Support Food Safety & Public Health

Share

FDA’s Oncologic Drugs Advisory Committee (ODAC) Votes to not Support Benefit/Risk Profile of Dacogen (decitabine) in Acute Myeloid Leukemia

In CategoryDrugs and Drug Companies
ByRuss Bianchi

Astex Pharmaceuticals, Inc. (NASDAQ:ASTX) today announced that the U.S. Food and Drug Administration’s (FDA’s) Oncologic Drugs Advisory Committee (ODAC) voted 10 to 3 with one person abstaining that data in our partner Eisai’s supplemental new Drug Application (sNDA) for DACOGEN® (decitabine) for Injection did not support a favorable benefit-risk profile for the treatment of acute myeloid leukemia (AML) in adults 65 years of age or older who are not considered candidates for induction therapy.

FDA’s Oncologic Drugs Advisory Committee (ODAC) Votes to not Support Benefit/Risk Profile of Dacogen (decitabine) in Acute Myeloid Leukemia

Share

FDA Finds Fungicide In Domestic Orange Juice

In CategoryBeverages, Toxins, Pollution, Contaminants, Chemicals, Etc
ByRuss Bianchi

Read my comments of late January 2012 blog postings on this subject and the FRAUD that is the vast majority of fruit brands and products.

~ Uncle Russ

The Food and Drug Administration says it has confirmed low levels of an illegal fungicide in orange juice samples taken from Florida manufacturers.

FDA Finds Fungicide In Domestic Orange Juice

Share

Repeat business? FDA approves new cancer drug to treat toxicity caused by another cancer drug

In CategoryCancer, Drugs and Drug Companies
ByRuss Bianchi

The US Food and Drug Administration (FDA) has approved a new cancer drug that allegedly treats the deadly side effects caused by another popular cancer drug.

Repeat business? FDA approves new cancer drug to treat toxicity caused by another cancer drug

 

Share

New FDA Approved Labeling For VYTORIN (Ezetimibe/Simvastatin) Includes Results From the Study of Heart and Renal Protection (SHARP) in Patients With Moderate to Severe Chronic Kidney Disease

In CategoryDrugs and Drug Companies
ByRuss Bianchi

Statins KILL, there are many MD authored books in the  recommended reading technical section of this web site proving statins are a complete FRAUD.

This retread approval is eugenics (genocide), period.

~ Uncle Russ

Merck (NYSE:MRK), known as MSD outside the United States and Canada, announced today that the U.S. Food and Drug Administration (FDA) has approved an updated label for VYTORIN® (ezetimibe/simvastatin) that includes results from the Study of Heart and Renal Protection (SHARP).

New FDA Approved Labeling For VYTORIN (Ezetimibe/Simvastatin) Includes Results From the Study of Heart and Renal Protection (SHARP) in Patients With Moderate to Severe Chronic Kidney Disease

Share

FDA Detains OJ Imports After Finding Fungicide

In CategoryBeverages, Toxins, Pollution, Contaminants, Chemicals, Etc
ByRuss Bianchi

Unless you are squeezing your own washed fresh fruit, you can rest assured your fruit powders, or fruit beverages, fruit juices, fruit tablets, fruit capsules, fruit chews, fruit drinks, fruit artificially fortified, fruit cocktails and/or blends, are tainted with residual harmful and toxic contaminants or artificial processes, like:

* acids (hydrochloric, phosphoric, carbolic sulfuric),

* alkalines (ammonia, chlorine, bromates),

* sterates,

* intestinal infecting microlaceration from added or foreign silicates,

* gravel and foreign undissolvable minerals leading to gall and kidney stones,

* inert gases (nitrogen, carbon monoxide or carbon dioxide),

* ultraviolet light degradation,

* sulfates and sulfites,

* chemical dehydration,

* cancer causing chemicals (sodium benzoate, potassium sorbate),

* fungicides,

* pesticides,

* herbicides,

* insecticides,

* plant defoliants (agent orange),

* foreign matter (bug parts, fecal matter dirt, dirty water, or plant material),

* petroleum and chemical based fertilizers,

* allergens,

* salts (nitrites, nitrates, phosphates),

* added caloric and harmful sweeteners,

* added flavors (artificial or not naturally occurring),

* added genetically modified organisms,

* added fake colors,

* chemical deionization,

* chemical or artificial clarification and filtering,

* chemical separation or physical centrifuging or high sheer molecular reformation,

* irradiation (cancer causing isotope exposure),

* pasteurization destroying enzymatic activity, as well as most or all nutrient absorbability,

* temperature treatments (confection enrobing, panning, starch mogul cooking, baking),

* excessive yeast,

* excessive mold,

* excessive bacteria,

* viruses,

* animal by products (gelatin capsules),

* plastic contamination from blow molded containers or rehydration with water from them (BPA, acrylamide),

* hormones,

* steroids,

* antibiotics,

* chemical preservatives, stabilizers, and emulsifiers,

* high intensity and alcohol distilled or polyol sweeteners,

* parasitical contaminants,

* rodents and rodent parts,

* heavy metals, toxic metals, non ferrous metal (mercury, lead, copper, aluminum),

* strychnine, arsenic, hemlock,

* neurotoxins,

* chemical distillants (alcohol, benzene, kerosene, glycerin, propylene glycol),

* purgatives and blood anti coagulants,

* toxic plant bark, roots, needles, saponins,

* residual pharmaceutical drugs found in municipal water used to hydrate fruit powders, fruit capsules, fruit tablets, or fruit drinks/juices/beverages,

* fluorine or fluoride,

* percolates,

* harsh freezing, canning, fluid bed drying (destroying nutrient content),

* petroleum and chemical bases waxes, sealants, or coatings,

* aseptic cooking and harsh dwell temperatures,

to name only a few ways to stop fruits, fruit juices/beverages, or fruit powders from fermenting into beer, wine, alcohol or rotting.

Chemistry does not lie, fake and hyped fruit product brands and their purveyors do.

~ Uncle Russ

The Food and Drug Administration has detained several shipments of imported orange juice after finding traces of an illegal fungicide.

FDA Detains OJ Imports After Finding Fungicide

Share

FDA Ups Testing For Fungicide In Orange Juice

In CategoryBeverages, Toxins, Pollution, Contaminants, Chemicals, Etc
ByRuss Bianchi

Unless you are juicing your own fruit, do NOT drink processed fruit juices, or unwashed fresh fruits loaded with genetically modification or pesticides, herbicides, insecticides, as well as fungicides.

Any fruit juice cocktails, or bottled concoctions, or powders, or fruit capsules, are NOT ABSORBABLE in any remaining or existing or added nutrients, antioxidants, minerals, vitamins or wellness benefit!

These fake fruit offering have been heated, pasteurized, clarified, emulsified, stripped, acidified, filtered, centrifuged, flash frozen, dried, fake fortified, artificially pH altered, fake colored, fake sweetened, fake flavored, vacuum or freeze dried, reconstituted, concentrated, and chemically manipulated, plus other harmful added excipients added.

Want real 100 percent absorbable wellness nutrients?

GOT ZIJA?!

~ Uncle Russ

The Food and Drug Administration says it will step up testing for a fungicide that has been found in low levels in orange juice.

FDA Ups Testing For Fungicide In Orange Juice

Share

F.D.A. halts imported orange juice shipments

In CategoryBeverages
ByRuss Bianchi

First the FDA and USDA ignore contamination in imported orange juice, then they deflected claiming there was no problem and now are halting imports.

These guys are the Keystone Kops…you cannot trust these guys…

Fraud
Deceit
Always

~ Uncle Russ

The Food and Drug Administration has halted shipments of imported orange juice from all over the world as the result of positive testing of the fungicide carbendazim.

F.D.A. halts imported orange juice shipments

Share

Exposed: Food manufacturers, not the FDA, have self-approved thousands of food chemicals in widespread use today

In CategoryFood and More
ByRuss Bianchi

Uncle Sam wants you DEAD prior to you 16th Social Security Ponzi Scheme Check.  Vote accordingly.

~ Uncle Russ

There are currently more than 10,000 chemical food additives permitted for use in foods today.

Share

FDA Demands End to Controversial Diet Plan

In CategoryDiet, Government
ByRuss Bianchi

HCG Harms

~ Uncle Russ

CNN’s Joe Johns talks to a weight loss physician about the FDA’s demand to halt over-the-counter sales of HCG diets.

FDA Demands End to Controversial Diet Plan

Share

FDA Drug Safety Communication: Safety Review of a Reported Death after the First Dose of Multiple Sclerosis Drug Gilenya (fingolimod)

In CategoryDrugs and Drug Companies
ByRuss Bianchi

The U.S. Food and Drug Administration (FDA) has received a report of a patient with multiple sclerosis (MS) who died within 24 hours of taking the first dose of Gilenya (fingolimod).

FDA Drug Safety Communication: Safety Review of a Reported Death after the First Dose of Multiple Sclerosis Drug Gilenya (fingolimod)

Share

Ranbaxy Settles with FDA over Manufacturing

In CategoryDrugs and Drug Companies
ByRuss Bianchi

Indian pharmaceutical giant Ranbaxy Laboratories Ltd. said Tuesday that it has signed a settlement with the U.S. Food and Drug Administration, committing to bolster its product manufacturing practices.

Ranbaxy Settles with FDA over Manufacturing

Share

FDA adds new heart warning to Sanofi’s Multaq

In CategoryCardiovascular Health, Drugs and Drug Companies
ByRuss Bianchi

Federal health officials have added new safety warnings to the heart rhythm drug Multaq after company studies linked the pill to higher rates of heart attack, stroke and death in a subset of patients.

FDA adds new heart warning to Sanofi’s Multaq

Share

FDA revisits safety of newer birth control drugs

In CategoryDrugs and Drug Companies
ByRuss Bianchi

Drugs KILL, Plants CURE.

~ Uncle Russ

Birth control drugs that were heavily promoted as having fewer side effects and the ability to clear up acne and other hormonal bothers are under new scrutiny from safety regulators.

FDA revisits safety of newer birth control drugs

Share

FDA warns 8 manufacturers for failing to register plants

In CategoryDrugs and Drug Companies
ByRuss Bianchi

This attached article demonstrates the very tip of a massive iceberg, of not only unregistered, but unregulated, or inspected drugs pouring into this country, with no oversight or safety testing whatsoever.

On a daily basis there is economic adulteration occurring in overseas plants, with harmful deadly raw materials and poor production practices, in mainstream drug brands sold in the USA (fact, not fiction, so don’t be fooled otherwise).

This attached article proves there is no safety protection for consumers by “FDA Approval” of drugs; registration is not inspection, or assurance of any compliance, let alone any consumer safety.

Drugs KILL. Plants CURE.

~ Uncle Russ

The US FDA has sent warning letters to eight biopharma companies for failing to register production facilities.

FDA warns 8 manufacturers for failing to register plants

Share

Take action NOW to stop FDA from turning your vitamins and supplements into unapproved ‘food additives’

In CategoryVitamins
ByRuss Bianchi

We here at NaturalNewscannot stress enough how important it is to take the time to fight back against the US Food and Drug Administration’s (FDA) latest assault against vitamins and dietary supplements.

Share

FDA Wants More Risk Information on Yaz Pills

In CategoryDrugs and Drug Companies
ByRuss Bianchi

Federal health experts said Thursday that drug labeling for Yaz and other widely-used birth control pills should be updated to emphasize recent data suggesting a higher risk of blood clots with the drugs than older contraceptive pills.

FDA Wants More Risk Information on Yaz Pills

Share

FDA Finds Serious Problems At Cancer Drug Plant

In CategoryCancer, Drugs and Drug Companies, Plants, Spices, Etc
ByRuss Bianchi

Cancer KILLS, Plants CURE.

~ Uncle Russ

Federal inspectors say the contract manufacturer for Johnson & Johnson’s cancer drug Doxil hasn’t been maintaining equipment or promptly investigating defective product batches and other serious problems at its Bedford, Ohio, factory.

FDA Finds Serious Problems At Cancer Drug Plant

Share

BMJ admits that fraud claim against Dr. Andrew Wakefield has no basis in fact

In CategoryUncategorized
ByRuss Bianchi

Big Pharma, the FDA, AMA and other medical associations falsely accuse conscientious healers of crimes that they themselves routinely commit or cover up.

BMJ admits that fraud claim against Dr. Andrew Wakefield has no basis in fact

Share

FDA Warns Novartis on 3 Manufacturing Facility Sites

In CategoryDrugs and Drug Companies
ByRuss Bianchi

Drugs KILL, Plants CURE.

~ Uncle Russ

The FDA today posted on its website a warning letter sent to Novartis International regarding 3 manufacturing facilities located in the U.S. and Canada. The letter is below.

FDA Warns Novartis on 3 Manufacturing Facility Sites

Share

FDA Issues Warning Letter to Mylan over Manufacturing Violations

In CategoryBusiness, Government
ByRuss Bianchi

The Truth Is Until There Are Body Counts No One Is Watching Or Monitoring Drug Safety.

Read THE TRUTH ABOUT THE DRUG COMPANIES by Dr. Marcia Angell, MD, recently retired Editor and Chief of THE NEW ENGLAND JOURNAL OF MEDICINE, and you will afraid to take a bay aspirin (which by the way is fraud propaganda for AG Bayer to harm you to sell you more drugs).

~ Uncle Russ

The FDA issued a warning letter to Mylan for “significant violations” of manufacturing rules identified during a February inspection of a manufacturing plant in Caguas, Puerto Rico.

FDA Issues Warning Letter to Mylan over Manufacturing Violations

Share

FDA May Modify Rule on Arsenic in Juice

In CategoryBeverages, Toxins, Pollution, Contaminants, Chemicals, Etc
ByRuss Bianchi

Uncle Sam Is A Pimp (the US House and US Senate).

Uncle Sam wants you dead.

Uncle Sam is in the nuke power business, arm and war business, genetically modified seed-crop-plant and livestock and poultry business, chemically and cancer causing laden grocery and beverage business, the tobacco business, the alcohol business, the meat packing and stripped dairy business, the heavy and toxic metals business, the tobacco business, the illegal and prescription harmful and deadly drug business, the harmful cleaning product and cosmetic business, the deadly high intensity sweetener business, the petroleum eco terrorism business, the serial ponzi scheme business (Madoff, Fannie Mae and Mack, Wall Street and Bank Taxpayer Bailouts, Social Security, Medicare, Obamacare, TSA, etc.)

This arsenic rule change, in the attached article, is a sad little splash in comparison to the TSUNAMI of poisons all incumbents in Congress and Uncle Sam have been bought off on, killing you and your family sooner, starting with public enemy number one, High Fructose Corn Syrup.

Vote Accordingly.

Merry Christmas!

~ Uncle Russ

In the wake of a Consumer Reports study that found levels of arsenic that exceeded the federal standards for bottled water (10 parts per billion, or ppb) in about 10% of sampled apple and grape juices, the FDA has said it will consider tightening its restrictions on arsenic levels in juice.

FDA May Modify Rule on Arsenic in Juice

Share

FDA: Avastin Not Shown to Be Safe and Effective in Breast Cancer Patients

In CategoryCancer, Drugs and Drug Companies
ByRuss Bianchi

FDA Commissioner Margaret A. Hamburg, M.D., said today she is revoking the agency’s approval of the breast cancer indication for Avastin  (bevacizumab) after concluding that the drug has not been shown to be safe and effective for that use.

FDA: Avastin Not Shown to Be Safe and Effective in Breast Cancer Patients

Share

FDA violates law by refusing to ban antibiotics from use in animal feed

In CategoryAnimals, Insects, etc, Drugs and Drug Companies
ByRuss Bianchi

Earlier in the year, several concerned groups sued the US Food and Drug Administration (FDA) for failing to address the issue of antibiotic use in animal feed.

Share

FDA ties birth control drugs to blood clot risk

In CategoryDrugs and Drug Companies
ByRuss Bianchi

Birth Control drugs also cause CANCER.

~ Uncle Russ

Federal health regulators say several new birth control drugs, including the Bayer pill Yaz, appear to increase the risk of dangerous blood clots more than older medications.

FDA ties birth control drugs to blood clot risk

Share

FDA: Possible to overdose on black licorice

In CategoryFood and More
ByRuss Bianchi

If the licorice root, or fake licorice flavoring and coloring, does not get you, the corn syrup and high fructose corn syrup will.

~ Uncle Russ

As it turns out, you really can overdose on candy—or, at least, black licorice.

The Food and Drug Administration (FDA) encourages moderation if you enjoy snacking on the old fashioned favorite, especially if you’re 40 or older.

FDA: Possible to overdose on black licorice

Share

FDA Considers Cracking Down On Arsenic In Juice

In CategoryBeverages, Toxins, Pollution, Contaminants, Chemicals, Etc
ByRuss Bianchi

You are in clear and present danger in the center aisles of any supermarket, the products are frankenfood.

~ Uncle Russ

The Food and Drug Administration is considering tightening restrictions for the levels of arsenic allowed in apple juice after consumer groups pushed the agency to crack down on the contaminant.

FDA Considers Cracking Down On Arsenic In Juice

Share