Showing posts with label Flu Shots. Show all posts
Showing posts with label Flu Shots. Show all posts

January 26, 2011

CBS: Flu Shots and Seizures

You know that "CBS Cares" PR line. I know they are just a huge Viacom congolmco, bit I am kinda starting to believe it a little. They seem to care about vaccine safety:

Child Flu Vaccine Seizures?
Posted by Sharyl Attkisson

More confusing news for parents trying to do the best, safest things for their children when it comes to vaccination.

According to a Vaccine Safety "update" issued by the FDA on Jan. 20, there's been an increase in reports of febrile seizures among infants and children following this year's flu vaccine. Febrile seizures are seizures associated with fever.

According to the FDA:

"FDA and CDC have recently detected an increase in the number of reports to VAERS of febrile seizures following vaccination with Fluzone (trivalent inactivated influenza vaccine or TIV, manufactured by Sanofi Pasteur, Inc.). Fluzone is the only influenza vaccine recommended for use for the 2010-2011 flu season in infants and children 6-23 months of age. These reported febrile seizures have primarily been seen in children younger than 2 years of age."

Read the rest here

August 25, 2010

Using Sex to Sell Vaccines

So this is happening:

Greeters and Admins needed for Mobile flu Clinic
posted: August 19, 2010, 03:05 PM

PUSH MODELS!!!!

Promotional Modeling Agency looking to hire Brand Ambassadors for an upcoming 6 week program. We are staffing a Mobile Flu Clinic that will be in Bangor Mall in Bangor, ME. We need outgoing, attractive, enthusiastic, and intelligent guys or girls between the ages of 18-30.

This is also a great opportunity for advancement in doing more promotional work. This program will run for 6 consecutive weekends (Saturdays and Sundays only). We are booking ambassadors for all 6 weekends, or every other weekend.

Please apply online at www.pushmodels.com. After you have filled out your profile, please email Amber Gordon at ag@pushmodels.com, put "Mobile Flu Clinic" in subject line, and specify that you will work in Bangor, ME.
Salary/Wage: $12/hr
Shift: Weekends

• Location: Bangor

Hot chicks that sell beer and cars... now used to sell vaccines.

Brought to you by the super ethical folks at Well Check.

Their web site is a "coming soon" page and their phone number only gets you a voice mail. Let's see if they return my call.

July 23, 2010

Unwanted H1N1 Vaccines Are HAZMAT And Are Being Disposed Of Accordingly

At the beginning of last years pharma fund raiser "pandemic", I wrote a lengthy piece reminding readers just how bad mercury really is to humans, and just how high the mercury content in the H1N1 flu shot was. These are the same vaccines that public heath officials keep referring to has having 'trace amounts' of mercury. I noted that they were so mercury toxic that they were classified as hazardous material and by law must be disposed of according to hazmat rules.

Now on the other side of the disease that killed ninety thousand Americans was the mildest flu in recorded history, more than $260 million dollars worth of vaccine, at least 40 million doses, are being disposed of accordingly. Being burnt in hazmat processing facilities with mercury scrubbers to keep this neurotoxin out of our environment.

Which again begs the question.... When we work so hard to keep mercury out of our waterways, WHY ARE WE PUTTING THIS POISON INTO OUR BABIES ON PURPOSE!!!!! IT IS ACTUAL HAZARDOUS MATERIAL!!! IT KILLS BRAIN CELLS!!! IT CAUSES MITOCHONDRIAL DISORDERS!!!!

Now I am going to be up all night worrying that the poor guy that has to burn all these vaccines is going to end up with Minamata Disease.

From Occupational Health and Safety Magazine:

Service Will Incinerate Unused H1N1 Vaccine
Jul 23, 2010

Clean Harbors, based in Norwell, Mass., is offering the service to health care providers because multiple doses of the vaccine contain enough mercury-based Thimerosal to be treated as a hazardous waste.

Clean Harbors of Norwell, Mass., now offers H1N1 Vaccination Incineration Services that will profile, collect, and dispose of unused 2009 H1N1 vaccine for health care customers nationwide. Multiple doses of the vaccine contain enough mercury-based Thimerosal to be treated by EPA as a hazardous waste and will be incinerated. Vaccine dated at the end of 2008 and early 2009 is now at the end of its shelf life and must be disposed, according to the company.

The HHS declaration of a 2009 H1N1 Public Health Emergency expired on June 23.

"We have seen many customers in various states looking for our H1N1 disposal capabilities," John C. Kelsey, the company's vice president, Healthcare Services, said in a July 22 e-mailed reply to questions about the service. "We wanted to announce it to the larger community as we are growing our customer count related to Healthcare Services. We have done a good amount of work in this area with vaccines through our hospital Pharmaceutical Waste programs."

He said the cost varies but is "generally the same pricing as other materials requiring hazardous waste incineration. The vaccine doses are in inventory and will be shipped via DOT packages for proper disposal," Kelsey added. "We are seeing multiple truckloads per week of the vaccine now and cannot align total amounts but we do expect the need to occur from many locations as the normal pathway for outdated items."
OLFA North America

Unused vaccine doses normally are returned through Reverse Distributors, but these have no value and thus must be disposed as a waste, he said, continuing, "It is good that PHER funds can be used to reimburse organizations for the disposal process."

CDC mandates proper disposal of H1N1 vaccines and allows Public Health Emergency Response (PHER) funds to be available for the disposal. Health care providers interested in the service can call 888-304-7035, e-mail healthcareservices@cleanharbors.com, or visit www.cleanharbors.com/healthcare.

There is a saying in our community....

Giving Mercury to Children on Purpose is Stupid

July 19, 2010

Dr. Blaylock's Advice on How To Reduce Chance of Adverse Reaction From Flu Shot

Treatment for Toxic Vaccine Exposure, from Russell Blaylock, M.D.

The Following was composed by Dr. Russell Blaylock as a method to reduce autoimmune reactions to the flu vaccines only. Do not use this if you have the flu itself. These are just general observations and not medical advice. You should work with your doctor for a specific program.Treatment for Toxic Vaccine Exposure

1. Place a cold compress on the site of the injection immediately after the injection and continue this as often as possible for at least two days. If symptoms of fever, irritability, fatigue or flu-like symptoms reoccur -- continue the cold compresses until they abate. A cold shower or bath will also help.

2. Take fish oils -- I recommend the Norwegian fish oil made by Carlson Labs -- it has the correct balance of EPA and DHA to reduce the cytokine storm. The dose is one tablespoon a day -- if severe symptoms develop -- two tablespoons a day until well and then switch to one tablespoon a day. Children -- one teaspoon a day.

3. Curcumin, quercetin, ferulic acid and ellagic acid as a mixture -- the first two must be mixed with extravirgin olive in one teaspoon. Take the mix three times a day (500 mg of each)

4. Vitamin E (natural form) 400 IU a day (high in gamma-E)

5. Vitamin C 1000 mg four times a day

6. Astaxanthin 4 mg a day

7. Zinc 20 mg a day for one week then 5 mg a day

8. Avoid all immune stimulating supplements (mushroom extracts, whey protein) except beta-glucan -- it has been shown to reduce inflammation, microglial activation and has a reduced risk of aggravating autoimmunity, while increasing antiviral cellular immunity.

9. Take a multivitamin/mineral daily (one without iron -- Extend Core)

10. Magnesium citrate/malate 500 mg of elemental magnesium two capsules three times a day

11. Vitamin D3:

All Children -- 5000 IU a day for two weeks after vaccine then 2000 IU a day thereafter

Adults -- 20,000 IU a day after vaccine for two weeks then 10,000 IU a day thereafter

Take 500 mg to 1000 mg of calcium citrate a day for adults and 250 mg a day for children under age 12 years.

12. Avoid all mercury-containing seafood

13. Avoid omega-6 oils (corn, safflower, sunflower, soybean, canola and peanut oils)

14. Blenderize parsley and celery and drink 8 ounces twice a day

15. Take Jatoba tea extract (add 20 drops in on cup of tea) one day before the vaccine and the twice a day thereafter. (you can get it at http://www.iherb.com/Amazon-Therapeutics-Jatoba-1-oz-30-ml/14429?at=0) It is inexpensive.

June 11, 2010

CNN: Report: Swine flu could cause up to 90,000 U.S. deaths

... August 24, 2009

"WASHINGTON (CNN) -- The H1N1 flu virus could cause up to 90,000 U.S. deaths, mainly among children and young adults, if it resurges this fall as expected, according to a report released Monday by a presidential advisory panel.

The report urges speedier production of the H1N1 vaccine and the availability of some doses by September..."

Remember this bologna? I thought I would post it again now that the school year is through, and we have seen what kind of garbage/vaccine sales tools are put out by the President's Council of Advisors on Science and Technology.

Do you know how many people died in Maine from the H1N1 virus? 19.

Well sure the death rate in Maine was practically nill... it is a rural state... but what about a place like California, the most populous state in the nation? 579.

Virginia 37
Iowa 41
New Mexico 58
Illinois 111

Are we at 90,000 yet? Are we even approaching that 36,000 deaths per year that CDC claims die from the flu during a typical season?

Let's go ahead and skip to the grand total of all deaths in the US:

Laboratory Confirmed Influenza-Associated Deaths
(all types of flu and pneumonia)
from August 30 2009 to April 3, 2010

2,117


90,000
-2,117
87,883


Holdren was off by 98%

(Begs the question... what if you threw a pandemic, and nobody came?)

How exactly does President's Council of Advisors on Science and Technology show their faces in public? Why does co-chair John "sterilants in the drinking water" Holdren still have a job?

Estimates range that between four and eight billion dollars was spent on this "pandemic" just in the US. Only a quarter of the population took the shot, and more than 70 million doses are being thrown away (that is mercury.. toxic waste.. hazmat material).

If we were not living in bazzaro world, the media would be raving about the billions wasted, the public would be screaming for hearings and investigations and jail time for fraud, and Barack Obama would have fired all these people and apologized to the American public for this colossal disaster and fear campaign. But apparently Holdren has put quaaludes in the drinking water.

But the really exciting question is... HOW CAN WE MAKE SURE THAT WE GET THE H1N1 STRAIN EVERY YEAR! How awesome is it that CDC reports 36,000 deaths every year and we had less than a tenth of that this year! Why is CDC not partying in the street!? We have found the safest flu ever!!!

HOORAY FOR H1N1!

October 26, 2009

The Dangers of Mercury in the H1N1 Vaccine


Last night I attended a SAD 75 (a Maine school district) public meeting on the H1N1 response and school vaccine clinics. It was a strange experience for me, as I feel like I had stepped back in time to a day ten years ago when giving mercury to children was no big deal, perfectly safe, just like candy really.

I pointed out a number of problems with doing so, which I assumed were common knowledge, that proved at the very least that mercury containing vaccines were not desirable and I will list some of those here for those of you who watched the meeting on TV and wanted references to my points.

As I want every parent and individual to have the informed consent that I was not given in vaccinating my child, I will also list several other references.

And if you have not read it already, this is a good time to review my "History of Thimerosal" (needs updating since 2007)


First, a reminder of what mercury does in the brain:




CDC's toxicology division, ATSDR, says that this is what mercury can do to children:

How does mercury affect children?

Very young children are more sensitive to mercury than adults. Mercury in the mother's body passes to the fetus and may accumulate there. It can also can pass to a nursing infant through breast milk. However, the benefits of breast feeding may be greater than the possible adverse effects of mercury in breast milk.

Mercury's harmful effects that may be passed from the mother to the fetus include brain damage, mental retardation, incoordination, blindness, seizures, and inability to speak. Children poisoned by mercury may develop problems of their nervous and digestive systems, and kidney damage.

And they have set up a new web site to warn children of the dangers of mercury complete with scary video:

Don't Mess With Mercury


A reminder of the damage that mercury does in the body:

Mercury impairs the immune system at a tiny fraction of the dose that is in vaccines:

Uncoupling of ATP-mediated Calcium Signaling and Dysregulated IL-6 Secretion in Dendritic Cells by Nanomolar Thimerosal

Environmental Health Perspectives, July 2006.

Samuel R. Goth, Ruth A. Chu Jeffrey P. Gregg

This study demonstrates that very low-levels of Thimerosal can contribute to immune system disregulation.

Excerpt: "Our findings that DCs primarily express the RyR1 channel complex and that this complex is uncoupled by very low levels of THI with dysregulated IL-6 secretion raise intriguing questions about a molecular basis for immune dyregulation and the possible role of the RyR1 complex in genetic susceptibility of the immune system to mercury."

The type of mercury in vaccines becomes trapped in the brain at higher rates than ingested mercury from fish:

Comparison of Blood and Brain Mercury Levels in Infant Monkeys Exposed to Methylmercury or Vaccines Containing Thimerosal

Environmental Health Perspectives, Aug 2005.

Thomas Burbacher, PhD [University of Washington].

Thimerosal is a preservative that has been used in manufacturing vaccines since the 1930s. Reports have indicated that infants can receive ethylmercury (in the form of thimerosal) at or above the Environmental Protection Agency (EPA) guidelines for methylmercury (MeHg) exposure, depending on the exact vaccinations, schedule, and size of the infant. This study compared the systemic disposition and brain distribution of total and inorganic mercury in infant monkeys following thimerosal exposure with infants exposed to MeHg. Monkeys were exposed to MeHg (via oral gavage) or vaccines containing thimerosal (via i.m. injection) at birth and 1, 2, and 3 weeks of age. Total blood mercury (Hg) levels were determined 2, 4 and 7 days after each exposure. Total and inorganic brain Hg levels were assessed 2, 4, 7 or 28 days after the last exposure.

The initial and terminal half-life of Hg in blood following thimerosal exposure was 2.1 and 8.6 days, which are significantly shorter than the elimination half-life of Hg following MeHg exposure at 21.5 days. Brain concentrations of total Hg were significantly lower by ~3-fold for the thimerosal-exposed infants when compared to the MeHg infants, while the average brain-to-blood concentration ratio was slightly higher for the thimerosal-exposed infants (3.5±1.0 vs. 2.5±0.6). A higher percentage of the total Hg in the brain was in the form of inorganic mercury for the thimerosal-exposed infants (34% vs 7%). The current study indicates that MeHg is not a suitable reference for risk assessment from exposure to thimerosal derived Hg. Knowledge of the toxicokinetics and developmental toxicity of thimerosal is needed to afford a meaningful assessment of the developmental effects of thimerosal-containing vaccines.

It causes neuro-inflammation (ie, rapid brain growth) by activating "glial" cells in the brain:

Increases in the number of reactive glia in the visual cortex of Macaca fascicularis following subclinical long-term methyl mercury exposure.

Toxicology and Applied Pharmacology, 1994

Charleston JS, Bolender RP, Mottet NK, Body RL, Vahter ME, Burbacher TM., Department of Pathology, School of Medicine, University of Washington

The number of neurons, astrocytes, reactive glia, oligodendrocytes, endothelia, and pericytes in the cortex of the calcarine sulcus of adult female Macaca fascicularis following long-term subclinical exposure to methyl mercury (MeHg) and mercuric chloride (inorganic mercury; IHg) has been estimated by use of the optical volume fractionator stereology technique. Four groups of monkeys were exposed to MeHg (50 micrograms Hg/kg body wt/day) by mouth for 6, 12, 18, and 12 months followed by 6 months without exposure (clearance group). A fifth group of monkeys was administered IHg (as HgCl2; 200 micrograms Hg/kg body wt/day) by constant rate intravenous infusion via an indwelling catheter for 3 months. Reactive glia showed a significant increase in number for every treatment group, increasing 72% in the 6-month, 152% in the 12-month, and 120% in the 18-month MeHg exposed groups, and the number of reactive glia in the clearance group remained elevated (89%). The IHg exposed group showed a 165% increase in the number of reactive glia. The IHg exposed group and the clearance group had low levels of MeHg present within the tissue; however, the level of IHg was elevated in both groups. These results suggest that the IHg may be responsible for the increase in reactive glia. All other cell types, including the neurons, showed no significant change in number at the prescribed exposure level and durations. The identities of the reactive glial cells and the implications for the long-term function and survivability of the neurons due to changes in the glial population following subclinical long-term exposure to mercury are discussed.

It impairs methylation, a biological process that creates the compound gluthatione, that allows the body to process out toxic substances:
Activation of Methionine Synthase by Insulin-like Growth Factor-1 and Dopamine: a Target for Neurodevelopmental Toxins and Thimerosal

Molecular Psychiatry, July 2004.

Richard C. Deth, PhD [Northeastern University].

This study demonstrates how Thimerosal inhibits methylation, a central driver of cellular communication and development. Excerpt:

"The potent inhibition of this pathway [methylation] by ethanol, lead, mercury, aluminum, and thimerosal suggests it may be an important target of neurodevelopmental toxins."

Thimerosal, at a fraction of the dose found in vaccines, causes motochondrial damage so severe, that it causes the cell actually self-destruct:

Thimerosal induces neuronal cell apoptosis by causing cytochrome c and apoptosis-inducing factor release from mitochondria.

International Journal of Molecular Medicine, 2006

Yel L, Brown LE, Su K, Gollapudi S, Gupta S.Department of Medicine, University of California, Irvine, CA 92697, USA. lyel@uci.edu

There is a worldwide increasing concern over the neurological risks of thimerosal (ethylmercury thiosalicylate) which is an organic mercury compound that is commonly used as an antimicrobial preservative. In this study, we show that thimerosal, at nanomolar concentrations, induces neuronal cell death through the mitochondrial pathway. Thimerosal, in a concentration- and time-dependent manner, decreased cell viability as assessed by calcein-ethidium staining and caused apoptosis detected by Hoechst 33258 dye. Thimerosal-induced apoptosis was associated with depolarization of mitochondrial membrane, generation of reactive oxygen species, and release of cytochrome c and apoptosis-inducing factor (AIF) from mitochondria to cytosol. Although thimerosal did not affect cellular expression of Bax at the protein level, we observed translocation of Bax from cytosol to mitochondria. Finally, caspase-9 and caspase-3 were activated in the absence of caspase-8 activation. Our data suggest that thimerosal causes apoptosis in neuroblastoma cells by changing the mitochondrial microenvironment.

Mitochondrial mediated thimerosal-induced apoptosis in a human neuroblastoma cell line (SK-N-SH).

Neurotoxicology. 2005

Humphrey ML, Cole MP, Pendergrass JC, Kiningham KK. Department of Pharmacology, Joan C. Edwards School of Medicine, Marshall University, Huntington, WV 25704-9388, USA.
Environmental exposure to mercurials continues to be a public health issue due to their deleterious effects on immune, renal and neurological function. Recently the safety of thimerosal, an ethyl mercury-containing preservative used in vaccines, has been questioned due to exposure of infants during immunization. Mercurials have been reported to cause apoptosis in cultured neurons; however, the signaling pathways resulting in cell death have not been well characterized. Therefore, the objective of this study was to identify the mode of cell death in an in vitro model of thimerosal-induced neurotoxicity, and more specifically, to elucidate signaling pathways which might serve as pharmacological targets. Within 2 h of thimerosal exposure (5 microM) to the human neuroblastoma cell line, SK-N-SH, morphological changes, including membrane alterations and cell shrinkage, were observed. Cell viability, assessed by measurement of lactate dehydrogenase (LDH) activity in the medium, as well as the 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) assay, showed a time- and concentration-dependent decrease in cell survival upon thimerosal exposure. In cells treated for 24 h with thimerosal, fluorescence microscopy indicated cells undergoing both apoptosis and oncosis/necrosis. To identify the apoptotic pathway associated with thimerosal-mediated cell death, we first evaluated the mitochondrial cascade, as both inorganic and organic mercurials have been reported to accumulate in the organelle. Cytochrome c was shown to leak from the mitochondria, followed by caspase 9 cleavage within 8 h of treatment. In addition, poly(ADP-ribose) polymerase (PARP) was cleaved to form a 85 kDa fragment following maximal caspase 3 activation at 24 h. Taken together these findings suggest deleterious effects on the cytoarchitecture by thimerosal and initiation of mitochondrial-mediated apoptosis.

And mercury leads to heart disease:

Mercury Activates Vascular Endothelial Cell Phospholipase D through Thiols and Oxidative Stress

Thomas J. Hagele, Jessica N. Mazerik, Anita Gregory, Bruce Kaufman, Ulysses Magalang, M. Lakshmi Kuppusamy, Clay B. Marsh, Periannan Kuppusamy, Narasimham L. Parinandi,

Lipidomics and Lipid Signaling Laboratory, Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Internal Medicine, The Ohio State University College of Medicine, Columbus, Ohio, United States

Correspondence: Address correspondence to Narasimham L. Parinandi, PhD, Room 611-A, Division of Pulmonary, Critical Care, and Sleep Medicine, Dorothy M. Davis Heart and Lung Research Institute, The Ohio State University, 473 W. 12th Avenue, Columbus, OH 43210, USA. E-mail:narasimham.parinandi@osumc.edu

Currently, mercury has been identified as a risk factor of cardiovascular diseases among humans. Here, the authors tested the hypothesis that mercury modulates the activity of the endothelial lipid signaling enzyme, phospholipase D (PLD), which is an important player in the endothelial cell (EC) barrier functions. Monolayers of bovine pulmonary artery ECs (BPAECs) in culture, following labeling of membrane phospholipids with [32P]orthophosphate, were exposed to mercuric chloride (inorganic form), methylmercury chloride (environmental form), and thimerosal (pharmaceutical form), and the formation of phosphatidylbutanol as an index of PLD activity was determined by thin-layer chromatography and liquid scintillation counting. All three forms of mercury significantly activated PLD in BPAECs in a dose-dependent (0 to 50 µM) and time-dependent (0 to 60 min) fashion. Metal chelators significantly attenuated mercury-induced PLD activation, suggesting that cellular mercury-ligand interaction(s) is required for the enzyme activation and that chelators are suitable blockers for mercury-induced PLD activation. Sulfhydryl (thiol-protective) agents and antioxidants also significantly attenuated the mercury-induced PLD activation in BPAECs. Enhanced reactive oxygen species generation, as an index of oxidative stress, was observed in BPAECs treated with methylmercury that was attenuated by antioxidants. All the three different forms of mercury significantly induced the decrease of levels of total cellular thiols. For the first time, this study revealed that mercury induced the activation of PLD in the vascular ECs wherein cellular thiols and oxidative stress acted as signal mediators for the enzyme activation. The results underscore the importance of PLD signaling in mercury-induced endothelial dysfunctions ultimately leading to cardiovascular diseases.

(More studies on the damage that vaccination and their components are known to do)


CDC reports that approximately 100 children die of the flu every year.

It was reported by the panel that 40-50 children die of flu per year, and that the 86 that have died from H1N1 this far had vastly exceeded that number. I told the panel that my understanding was that the number was 100 per year, and that we had not yet exceeded that. I had gotten that number from this CDC video that was posted a year ago on their You Tube Channel (50 seconds in Dr. Jeanne Santoli states that about 100 children die of influenza every year).




They have either doubled the real number, or cut it in half, presumably to encourage vaccination.

So my question is... was CDC inflating the number of children who die per year from the flu last year to scare parents into getting the seasonal flu vaccine OR are they deflating number of children who die per year from the flu this year to scare parents into getting the H1N1 vaccine?

[Update: CDC has reported that pediatric flu deaths have ranged between 46 and 153 over the last six years. CDC has apparently chosen the lowest year of pediatric flu deaths to use as their "average" to make this years flu deaths seem like they are twice the 'average'.

How many children have died from flu-associated complications during previous flu seasons?

* During the 2003-04 season, 153 flu-associated deaths in children were reported to CDC. (This data was collected by CDC.)
* During the 2004-05 season, 47 deaths in children were reported to CDC. (This is the first year that influenza mortality in children became a nationally reportable condition.)
* During the 2005-06 season, 46 deaths in children were reported to CDC.
* During the 2006-07 season, 76 deaths in children were reported to CDC.
* As of June 14, 2008, 83 deaths in children occurring during the 2007-08 season have been reported to CDC.

(Note: The counts above are of flu-associated deaths among children according to the flu season the deaths occur, not when they are reported to CDC.)

So pediatric deaths over the last 5 years average 81.

In Maine, no children have died from the flu this year, despite the fact that it has been one of top three states where the virus first became widespread.

It should also be noted that CDC is currently stonewalling a CBS News request for accurate H1N1 flu numbers. Additionally, CDC turned down a request to expidite CBS's FOIA request for the information on state H1N1 numbers because CDC has determined the request is “not a matter of widespread and exceptional media and public interest.”

Read that again... accurate numbers on H1N1 are “not a matter of widespread and exceptional media and public interest.”]


Thimerosal Containing Vaccines are legally classified as Hazardous Materials

Because of the mercury content in these vaccines, they cannot be thrown away, or even disposed of according to medical waste guidelines. To do so would be illegal.

They must be disposed of according to HazMat rules. From the Wisconsin guidelines:

Some vaccines are preserved with 1:10,000 or 0.01 percent Thimerosal (see the vaccines in the table titled "Thimerosal Content in Some U.S. Licensed Vaccines" at www.vaccinesafety.edu/thi-table.htm that have .01% in the Thimerosal Concentration column). Thimerosal contains about 50 percent mercury by weight. Vaccines with 1:10,000 or 0.01 percent Thimerosal have about 50 mg/L mercury, which exceeds the 0.2 mg/L hazardous waste toxicity characteristic regulatory level for mercury. According to state and federal hazardous waste management requirements, discarded Thimerosal-preserved vaccines may need to be managed as hazardous waste, using the waste code D009 (mercury).

It is illegal to manage Thimerosal-preserved vaccines as infectious waste or regular trash.

A (just in case) correction on my statement on mercury concentrations in vaccines. I may have said "parts per million" when I meant "parts per billion", but I can't remember.

None the less, the mercury concentration in the H1N1 and seasonal flu shots is exponentially larger than what is considered hazmat material. A comparison of mercury concentrations from Pediatrics:

0.5 parts per billion (ppb) mercury = Kills human neuroblastoma cells (Parran et al., Toxicol Sci 2005; 86: 132-140).

2 ppb mercury = U.S. EPA limit for drinking water http://www.epa.gov/safewater/contaminants/index.html#mcls

20 ppb mercury = Neurite membrane structure destroyed (Leong et al., Neuroreport 2001; 12: 733-37).

200 ppb mercury = level in liquid the EPA classifies as hazardous waste. http://www.epa.gov/epaoswer/hazwaste/mercury/regs.htm#hazwaste

25,000 ppb mercury = Concentration of mercury in the Hepatitis B vaccine, administered at birth in the U.S., from 1990-2001.

50,000 ppb Mercury = Concentration of mercury in multi-dose DTaP and Haemophilus B vaccine vials, administered 4 times each in the 1990's to children at 2, 4, 6, 12 and 18 months of age. Current "preservative" level mercury in multi-dose flu (94% of supply), meningococcal and tetanus (7 and older) vaccines. This can be confirmed by simply analyzing the multi- dose vials.

In my home state of Maine mercury disposal is regulated by The Hazardous Waste Rules Chapter 850

Maine Department of Environmental Protection

Chapter 850: IDENTIFICATION OF HAZARDOUS WASTES

B. Identification of hazardous wastes by characteristics

(5) Characteristic of toxicity

(b) A waste that exhibits the characteristic of toxicity has the EPA Hazardous Waste Number specified in Table I which corresponds to the toxic contaminant causing it to be hazardous.

Table I. Maximum Concentration of Contaminants for the Toxicity Characteristic

EPA Hazardous Waste No.: D009

Contaminant: Mercury

Regulatory Level (mg/L): 0.2 mg/L [0.2002 ppm] [200.2 ppb]

What this means is that if you took one of the vaccines being injected into the children at my son's elementary school outside and squirted it onto the pavement, a hazmat rules would be triggered and a hazmat team must be called in to clean it up.

[Update 07/23/10 - Now that the "pandemic" has passed, and so few decided to take this toxic vaccine, tens of millions of doses are being destroyed. As I said they must be, via hazmat rules. Clean Harbors in Norwell, MA is offering their services. Via Occupational Health and Safety Magazine:

Service Will Incinerate Unused H1N1 Vaccine
Jul 23, 2010

Clean Harbors, based in Norwell, Mass., is offering the service to health care providers because multiple doses of the vaccine contain enough mercury-based Thimerosal to be treated as a hazardous waste.

Clean Harbors of Norwell, Mass., now offers H1N1 Vaccination Incineration Services that will profile, collect, and dispose of unused 2009 H1N1 vaccine for health care customers nationwide. Multiple doses of the vaccine contain enough mercury-based Thimerosal to be treated by EPA as a hazardous waste and will be incinerated. Vaccine dated at the end of 2008 and early 2009 is now at the end of its shelf life and must be disposed, according to the company....


Hazardous materials do not belong in children. Period.]


EPA says you must weigh 550 lbs. to safely process the mercury in a flu vaccine

Thimerosal containing flu shots have 25 mcg of mercury in them.

EPA daily limits on mercury intake are .1 mcg per kilogram of weight. 1 kilo = 2.20462262 pounds My 55 pound 7 year old therefore weighs 25 kelograms.

25 x .1 = 2.5

The EPA says that my son should receive no more than 2.5 mcg of mercury in a day. The vaccine he will be offered at school contains ten times that amount.

I weigh 255 lbs or 116 kelos. 116 x .1 = 11.6

The vaccine is still more than twice what a big girl like me should be exposed to.

Further these EPA standards are based on ingested methyl mercury, the kind found in fish, (only about a tenth of which is absorbed through the GI tract into the blood stream). We have already seen from the Burbacher study above, that injected thimerosal becomes trapped in the brain at a much higher rate than ingested mercury. So the EPA standards I am using are probably should be upped by ten fold when being applied to vaccination.

EPA/FDA/CDC will not set safety limits for injected methyl mercury, despite the demand from parents for them to do so for many years.

No one has died from mercury

One of the panelists, a physician, suggested that no one has died from mercury in vaccines. This is a disingenuous statement as vaccine deaths are attributed to the vaccine as a whole, not to the components of the vaccine. And of course Death is a known outcome of vaccination and is covered under the HHS Vaccine Injury Compensation Program.

And yes... people have died from mercury.

Government agencies and states are trying to eliminate mercury in daily life, but it is still in vaccines.


Bills and laws limiting and eliminating mercury are ubiquitous now. It is the height of cognitive dissonance to say that mercury should be eliminated from the environment, but injected into babies as young as 6 months.

And all this is true BEFORE you even begin the discussion on whether or not mercury containing vaccines can cause autism. CDC has done only ONE study of the relationship between vaccines and autism. A HORRIBLE study. It took a very fat bestseller to explain just how many shenanigans went into this study. Julie Gerberding was finally forced to tell congress that the study methods were "useless" in answering the question, 'does mercury in vaccines cause autism', and she did it the cowards way... a quiet report that was leaked to a reporter a few months later. No formal retraction or apology has been issued and the study is still touted as proof that vaccines don't cause autism. Note that this paragraph is the first time the word "autism" is even appears in this piece. And the last.

Now consider the statements like this that CDC are making:

Dr. Anne Schuchat appearing on The Doctors - "Now the other questions people have...and.. .I get this all the time...is about mercury. It's about the Thimerosal preservative. I want to say there have been a lot of studies about that. There's no scientific link between the thimerosal preservative and any kind of long term problem".

CDC is lying about the safety of thimerosal. Don't trust them, don't trust me. Do your own research and fact check everyone. It is your health and the health of your family.


There is a saying in our community....

Giving Mercury to Children on Purpose is Stupid

October 9, 2008

Louise Rocks Fox and Friends Today

Louise Kuo Habakus and Claudine Liss from the New Jersey Coalition for Vaccine Choice were on Fox and Friends today and did a wonderful job of explaining why forced vaccination is a bad idea.

For the record, I can't remember seeing Fox News do anything on the vaccine autism connection, so props to the ladies for getting this interview!

Don't forget the Vaccine Choice Rally on October 16th.

March 14, 2008

Can I Get The Flu Shot While Pregnant?

(I have noticed a lot of people coming to my blog from the "Can I get the flu shot while pregnant" search term. They have been referred to another post of mine, "Did You Get The Flu Shot While Pregnant". Feel free to visit that post, which is on mom's reports of long term damage done to their kids from getting the flu shot, but I thought I should write something that more directly speaks to this question:)

The CDC and it's Advisory Committee on Immunization Practices (ACIP) recommends the flu shot for pregnant women.

However, I believe that this is an irresponsible recommendation as the flu shot has not been safety tested on pregnant women.

And despite the fact that some of these flu vaccines are not for use in children, the CDC and ACIP have not issued a warning for pregnant women not to have them.

Additionally, despite repeated requests from parents of vaccine injured children, the CDC and ACIP will not state a preference for pregnant women to receive only Thimerosal free flu shots.

From the vaccine package inserts:

Fluarix (Thimerosal free):
Pregnancy: Pregnancy Category C. Animal reproduction studies have not been conducted with FLUARIX. It is not known whether FLUARIX can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. FLUARIX should be given to a pregnant woman only if clearly needed. The ACIP has issued recommendations regarding the use of the influenza virus vaccine in pregnant women.

Nursing Mothers: It is not known whether FLUARIX is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when FLUARIX is administered to a nursing woman. The ACIP has issued recommendations regarding the use of the influenza virus vaccine in nursing mothers.

Pediatric Use: FLUARIX IS NOT INDICATED FOR USE IN CHILDREN.


Flulaval (Contains Thimerosal):
Pregnancy: Pregnancy Category C. Animal reproduction studies have not been conducted with FLULAVAL. It is also not known whether FLULAVAL can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. FLULAVAL should be given to a pregnant woman only if clearly needed.

Nursing Mothers: It is not known whether FLULAVAL is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when FLULAVAL is administered to a nursing woman.

Pediatric Use: Safety and effectiveness of FLULAVAL in pediatric patients have not been established.


Flumist (Thimerosal Free):
Pregnancy: Pregnancy Category C Animal reproduction studies have not been conducted with FluMist. It is not known whether FluMist can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. FluMist should be given to a pregnant woman only if clearly needed.
The effect of the vaccine on embryo-fetal and pre-weaning development was evaluated in a developmental toxicity study using pregnant rats receiving the frozen formulation. Groups of animals were administered the vaccine either once (during the period of organogenesis on gestation day 6) or twice (prior to gestation and during the period of organogenesis on gestation day 6), 250mcL/rat/occasion (approximately 110-140 human dose equivalents based on TCID50), by intranasal instillation. No adverse effects on pregnancy, parturition, lactation, embryo-fetal or preweaning development were observed. There were no vaccine related fetal malformations or other
evidence of teratogenesis noted in this study.

Nursing Mothers: It is not known whether FluMist is excreted in human milk. Therefore, as some viruses are excreted in human milk and additionally, because of the possibility of shedding of vaccine virus and the close proximity of a nursing infant and mother, caution should be exercised if FluMist is administered to nursing mothers.

Pediatric Use: FluMist is not indicated for use in children <24 months of age. FluMist use in children <24 months has been associated with increased risk of hospitalization and wheezing in clinical trials [see Warnings and Precautions (5.1) and Adverse Reactions (6.1)].



Fluvirin (Contains Thimerosal)
Pregnancy: Pregnancy Category C
Animal reproduction studies have not been conducted with Influenza Virus Vaccine (FLUVIRIN®). It is also not known whether Influenza Virus Vaccine (FLUVIRIN®) can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Influenza Virus Vaccine (FLUVIRIN®) should be given to a pregnant woman only if clearly needed.
The clinical judgment of the attending physician should prevail at all times in determining whether to administer Influenza Virus Vaccine to a pregnant woman.

Pediatric Use: The safety and immunogenicity of FLUVIRIN® have been established in the age group 4 years to 16 years. The use of FLUVIRIN® in these age groups is supported by evidence from adequate and well-controlled studies of FLUVIRIN® in adults that demonstrate the immunogenicity of FLUVIRIN®. The safety and immunogenicity of FLUVIRIN® have not been established in children <4 years of age.



Fluzone (Comes in both Thimerosal Containing and Thimerosal Free):
PREGNANCY CATEGORY C
Animal reproduction studies have not been conducted with Influenza Virus Vaccine. It is not known whether Influenza Virus Vaccine can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Influenza Virus Vaccine should be given to a pregnant woman only if clearly needed. For guidance regarding use in pregnant women, see INDICATIONS AND USAGE section.

PEDIATRIC USE: SAFETY AND EFFECTIVENESS OF FLUZONE VACCINE (SUBVIRION) IN INFANTS BELOW THE AGE OF 6 MONTHS HAVE NOT BEEN ESTABLISHED.

July 19, 2007

Just Say No To Mercury

Say 'No' to Mercury in Flu Shots
Opinion | Editorial
Savannah Morning News
greg powell | Thursday, July 19, 2007 at 12:30 am


Thimerosal is a mercury-based preservative used in most flu vaccines in our country.

You are filled with thoughts of joy as you sit down and roll up your sleeve. You want the very best for the new life that's growing inside you.

You want to do everything possible to ensure the health and safety of that precious child.

Then you feel a little stick in your arm. Good, now you've done one more thing to protect your baby.

Or have you?

You have no idea that you were just injected with one of the most toxic substances in the world.

This may sound like a cruel joke or just a science-fiction story, but I can assure you that this is a very real nightmare.

Thimerosal is a mercury-based preservative used in most flu vaccines in our country.

When injected into the human body, it quickly converts to a form of organic mercury, known as ethyl-mercury.

This form of mercury, like all forms of mercury, is extremely dangerous.

Numerous animal studies have proven the extreme toxicity of thimerosal.

Some studies have shown that thimerosal dramatically increases fetal deaths in rabbits and rats.

In pigs, ethyl-mercury was shown to cause neurological, urological, and digestive toxicity.

Other rat studies have shown that ethyl-mercury causes pathological lesions of the ovaries, uterus, testes, seminal vesicles, vas deferens and prostate.

In monkeys, injection of thimerosal was shown to cause mercury to deposit in the brain and stay there indefinitely.

Once in the brain, mercury can set in motion a cascade of events leading to a chronic state of inflammation in the brain and resulting in destruction of neurons.

As a pharmacist, I can tell you with absolute certainty that if we had these kinds of animal studies with any other drug, that drug would be recalled by the government immediately because of public safety.

The amount of mercury in one flu shot is 25 micrograms.

According to federal guidelines, a person would have to weigh about 550 pounds for this amount of mercury to be considered safe.

The heavy use of several thimerosal-containing childhood vaccines in the 1990s has been linked by some researchers to the epidemic levels of autism in our country.

I believe, like many parents of autistic children, that the large amounts of mercury these children received, when they were just tiny infants, caused brain damage leading to autism.

I also believe that there is a good chance that mercury from vaccines and other sources is a factor in many various other neurological disorders including Alzheimer's disease, Parkinson's disease and multiple sclerosis.

This information leads one to ask: Why is thimerosal still being used in flu shots, and why hasn't the government removed it?

I don't know the answer to that question.

What I can say is that, in my opinion, thimerosal is an extremely dangerous substance and has absolutely no place in any vaccine or in any other product that is used in or on the human body.

Contrary to this logic, the Centers for Disease Control in Atlanta, being fully aware of the dangers associated with mercury, aggressively promotes flu shots for pregnant women, children, the elderly and people with chronic health conditions.

Ironically, these are the very people who are most vulnerable to mercury toxicity.

Flu shots without mercury are available.

I encourage all people who are planning to get a flu shot, especially pregnant women, to request a flu shot which is free of mercury.

I also encourage health care providers to provide verbal informed consent to all patients to whom they are giving a thimerosal-containing influenza vaccine.

As health-care providers, we have a duty to ensure the safety and well-being of our patients.

Injecting patients with mercury is not a way to do that. This is not a chance we should take.

We should err on the side of caution.

Greg Powell is a Savannah pharmacist.

November 1, 2006

NAA Cites Serious Shortcoming in CDC Flu Shot Safety Study

PRESS RELEASE
For Immediate Release:
October 31, 2006

Contact:
Wendy Fournier, NAA (Portsmouth, RI) 401-632-7523
Lori McIlwain (Cary, NC) 919-468-6455


National Autism Association Cites Serious Shortcoming in CDC Flu Shot Safety Study
Six-week follow-up called “ridiculously inadequate” by autism advocacy group

Nixa, MO – A study published this week in the Journal of the American Medical Association indicating that the influenza vaccine is safe for infants and toddlers is being criticized for the brief six-week follow-up of subjects involved in the study. Funded by the Centers for Disease Control and Prevention (CDC), nine of the 19 authors admit ties with vaccine makers including Sanofi Pasteur, GlaxoSmithKline, and others.

“Following-up with these children for a mere six weeks is ridiculously inadequate,” according to National Autism Association (NAA) executive director Rita Shreffler. “The neurological injuries that result in diagnoses such as autism do not typically occur immediately after getting shots. Exposures to vaccine toxins such as mercury are cumulative and symptoms of injury may not be apparent for months or even years. Apparently, this is yet another CDC-drug company collaboration to whitewash thimerosal and ensure that flu shots are as profitable as possible, regardless of their long term adverse effects.”

Thimerosal is a mercury-based preservative used in most flu shots, including those often received by pregnant women and young children. While some mercury-free flu shots are manufactured each year, the majority contain 25 micrograms of mercury, an amount considered safe by the Environmental Protection Agency for an adult weighing 550 pounds. A growing number of scientific studies link mercury exposure in susceptible individuals to the development of neurological injuries such as autism and attention deficit hyperactivity disorder. The CDC now recommends the flu vaccine for pregnant women, and annually for children six months through five years of age.

At a meeting of the CDC’s Advisory Committee on Immunization Practices (ACIP) last week, thimerosal was not placed on the agenda despite a request from 15 national organizations that the ACIP follow the 2001 Institute of Medicine recommendations that pregnant women, infants, and children receive thimerosal-free vaccines. CDC officials also refused to vote on stating a preference for thimerosal-free vaccines for pregnant women and children.

“Pregnant women and young children shouldn’t be exposed to mercury in any form because of the potential for serious neurological injury,” commented Laura Bono, NAA board member and mother of a vaccine-injured son. “In my opinion, failure to follow-up appropriately with the kids in this study, then based on the incomplete data, promote flu vaccines as ‘safe,’ is irresponsible, giving parents a false sense of security. Predictably, this latest from the CDC does nothing to address the long-term dangers of injecting children with mercury.”

For more information on autism, visit www.nationalautism.org

October 31, 2006

Hg in Flu Vaccines - Print This Helpful Guide Out And Take To The Doc

List of flu shots that contain mercury:

Autism, mercury poisoning, thimerosal and the flu vaccine
public_health@8:22 am PST email to the editor
by Michael Dorausch, DC
planetc1.com news staff

About two weeks ago, news reports began showing up online suggesting that the flu vaccine was found safe to be used in children under the age of two.

The study looked at immunization records for more than 45,000 children and researchers determined that the intramuscular flu vaccine was safe to be used in children under the age of two.

According to the Centers for Disease Control and Prevention (CDC), "the single best way to protect against the flu is to get vaccinated each year" and the CDC now recommends children under the age of two receive the flu vaccine.

Hundreds of news articles began appearing on major web sites such as Google News, MSN, and Yahoo, touting the recently reported study and suggesting the vaccine was now safe for babies. The message was clear... get the shot, get the shot, get the shot. However, there was something missing that was not appearing in any of the news articles... flu shots contain thimerosal.

That may come as no big deal to some, but to a parent that has been fighting with vaccine manufacturers and/or government officials to get mercury compounds out of vaccines, it's a very big deal.

Thimerosal
After increased pressure from consumers, parents of autistic children groups, and government elected officials, vaccine manufacturers and the FDA have collectively agreed to begin removing thimerosal from childhood vaccines. Problem is, up until these recent recommendations, the flu vaccine was not considered a childhood vaccine.

Here is a list of FDA links with PDF document information on various intramuscular flu vaccines being used in 2006. Fluzone "No Preservative" pediatric dose by Aventis Pasteur, reports not to use thimerosal in the manufacturing process. Below that are some links to get more information about Thimerosal.

Fluvirin™ (Chiron Vaccines Ltd.)
Thimerosal (mercury derivative, =0.98 mcg mercury per 0.5 mL dose) is used in manufacture of the unit dose preservative free presentation but is reduced by the purification process to trace amounts.
http://www.fda.gov/cber/label/inflchi091405LB2.pdf

Fluarix™ (Influenza Virus Vaccine for intramuscular use)
Thimerosal is used at the early stages of manufacture and is removed by subsequent purification steps to <1.25 mcg mercury per dose.
http://www.fda.gov/CbER/label/inflgla083105LB.pdf

FLULAVAL™ (Influenza Virus Vaccine) ID Biomedical Corporation of Quebec (IDB)
FLULAVAL is an influenza virus vaccine indicated for active immunization of adults 18 years of age and older. Thimerosal, a mercury derivative, is added as a preservative. Each 0.5 mL dose contains 25 mcg mercury.
http://www.fda.gov/Cber/label/inflidb100506LB.pdf

Fluzone (Aventis Pasteur, Inc.)
Fluzone vaccine is supplied in four different presentations: a 5 mL vial of vaccine which contains the preservative thimerosal [(mercury derivative), (25 µg mercury/dose)]; a 0.25 mL prefilled syringe (No Preservative: Pediatric Dose, for 6 – 35 months of age) distinguished by a pink syringe plunger rod; a 0.5 mL prefilled syringe (No Preservative, for 36 months of age and older); and a 0.5 mL vial (No Preservative, for 36 months of age and older). There is no thimerosal used in the manufacturing process of the No Preservative unit dose presentations of Fluzone vaccine.
http://www.fda.gov/CbER/products/inflave071405.htm

Thimerosal in Vaccines (from the FDA)
http://www.fda.gov/Cber/vaccine/thimerosal.htm

Thimerosal (from Wikipedia) -- Thiomersal is a very toxic compound which is harmful by inhalation and ingestion.
http://en.wikipedia.org/wiki/Thimerosal

National Vaccine Information Center - Mercury Calculator
http://www.nvic.org/Issues/HgCalculator.htm

October 28, 2006

BMJ: Influenza Vaccine Programs May Be Pointless

Article in BMJ discounts the usefulness of the flu vaccine. Here is the BMJ article preceeded by Medical News Today's summary of it:

Influenza Vaccine Programs May Be Pointless
Main Category: Flu / SARS News
Article Date: 28 Oct 2006 - 0:00am (PDT)
Written by: Christian Nordqvist
Editor: Medical News Today

Influenza vaccination programs, which cost nations millions of dollars every year, could be a waste of time and money, says Dr. Tom Jefferson, Cochrane Vaccines Field, Rome, Italy. Jefferson says he hopes his findings will make North American and European taxpayers wonder whether the effort and expense are justified.

You can read about his findings in The British Medical Journal (BMJ), October 28.

In this study, Jefferson examined all published papers worldwide that reported on the effects of inactivated vaccines (vaccines with dead viruses). In other words, he studied the reviews of all studies. He concluded that flu shot campaigns have either no effect, or a very negligible effect, on the number of hospitalizations, work/school time lost, complications from flu, or death from flu.

Jefferson said "I looked at the evidence described by systematic reviews and confronted it with policy and I found that there is a massive gap. Almost none of the benefits that these policy documents list are actually given by inactivated vaccines or, if they are, they are given in slighter measure." He said he is not sure why this is so. He suggested it could be a result of inadequate surveillance systems, and/or diagnosing too many influenza-like respiratory illnesses as flu (when they are not). He added that "In most surveillance systems, you actually have an almost year-round epidemic which, in fact, is not influenza. It's caused by other agents." He criticized many of the studies he looked through, saying they were weak.

According to official figures (CDC), approximately 200,000 Americans get flu so badly each year that they have to be hospitalized - about 36,000 people die each year as a result of catching flu in the USA.

Jefferson said he was surprised to see such a large gap between vaccination campaign policy and evidence of its effectiveness.

"Influenza vaccination: policy versus evidence"
Tom Jefferson
BMJ 2006;333:912-915 (28 October), doi:10.1136/bmj.38995.531701.80



The BMJ article:

Public health

Influenza vaccination: policy versus evidence
Tom Jefferson, coordinator1

1 Cochrane Vaccines Field, Anguillara Sabazia, Roma 00061, Italy jefferson.tom@gmail.com

Each year enormous effort goes into producing influenza vaccines for that specific year and delivering them to appropriate sections of the population. Is this effort justified?

Viral infections of the respiratory tract impose a high burden on society. In the last half of the 20th century, efforts to prevent or minimise their impact centred on the use of influenza vaccines. Each year enormous effort goes into producing that year's vaccine and delivering it to appropriate sections of the population. Here, I will discuss policies on the use of inactivated vaccines for seasonal influenza; the evidence for their efficacy, effectiveness, and safety ("effects"); and possible reasons for the gap between policy and evidence.

Policies

Every vaccination campaign has stated aims against which its effects must be measured. The US Advisory Committee on Immunisation Practices produces a regularly updated rationale for vaccination against influenza.1 The current version identifies 11 categories of patients at high risk of complications from influenza (box).

The rationale rests on the heavy burden that influenza imposes on the population and the benefits of vaccination. For example, reductions in cases, admissions to hospital, mortality of elderly people in families with children, contacts with healthcare professionals, antibiotic prescriptions, and absenteeism for children and household contacts are the main arguments for extending vaccination to healthy children aged 6-23 months in the United States.2 Canada introduced a similar policy in 2004.3 Less comprehensive policies recommending vaccination for all people aged 60 or 65 and over are in place in 40 of 51 developed or rapidly developing countries.4 On the basis of single studies, the World Health Organization estimates that "vaccination of the elderly reduces the risk of serious complications or of death by 70-85%."5 Given the global nature of these recommendations, what type of evidence should we expect to support them and what does available evidence tell us?4

Which evidence?

When considering the best evidence for vaccination we must take into account the unique epidemiological features of influenza viruses and the rationale for immunisation. The incidence and circulation of seasonal influenza and other respiratory viruses vary greatly each year, each season, and even in each setting. A systematic review of the incidence of influenza in people up to 19 years' old reported a seasonal variability of 0-46%; during a five year period the average incidence was 4.6% in this age group. During a period of 25 years the incidence was 9.5% in children under 5.6 Because of this variability and lack of carryover protection from one year's vaccine to the next,7 especially if the virus changes its antigenic configuration, single studies reporting data from one or two seasons are difficult to interpret. Single studies are also not reliable sources for generalising and forecasting the effects of vaccines, especially when numbers are small. They introduce further instability into already problematic forecasting. Additional limitations to our forecasting ability are imposed by our use (and misuse) of studies assessing the effects of influenza vaccines. Although the effect assessed depends on the aims of the particular campaign, most concentrate on serious effects (such as pneumonia or death) and person to person transmission (table 1). Field efficacy studies are only relevant when viral circulation is high, but no one can forecast with precision the impact on next year's influenza.

December 9, 2005

Are U.S. Health Experts Inflating Flu Statistics?

Are U.S. Health Experts Inflating Flu Statistics?
By Ed Edelson
HealthDay Reporter

FRIDAY, Dec. 9 (HealthDay News) -- A Harvard grad student is charging that the U.S. government is hyping the threat of the annual (non-avian) strains of influenza. Specifically, Peter Doishi says, the estimate of 36,000 flu-related deaths a year by the Centers for Disease Control and Prevention is unsupported by the available data.
And, he suspects, the numbers may be inflated to help drug companies sell more flu vaccine.

It's a familiar charge -- a quick scan of the Internet turns up several Web sites claiming much the same thing -- and like many others who make the claim, Doshi is not a medical expert. He's a student in Harvard's department of East Asian studies.
But he presents his charges with one notable difference: They appear in the form of an article published in this week's issue of the prestigious British Medical Journal.
In his one-page article, Doshi lauded the BMJ's "system of open discussion and open debate through their on-line bulletin board ... a very democratic form of scientific discourse."

His criticism centers on a 2003 paper in the Journal of the American Medical Association in which CDC experts increased their estimate of flu-related deaths from 20,000 a year to 36,000 a year. The reasons the agency used to justify that rise are dubious at best, Doshi said.

For one thing, the National Center for Health Statistics lists only a few hundred deaths a year as directly caused by influenza, Doshi said. And the major explanation for the increased estimate -- the aging of the American population that puts more people in the highly vulnerable over-65 group -- doesn't hold water, he maintained.
"The 65-plus population grew just 12 percent between 1990 and 2000," Doshi wrote. How can the CDC justify an estimate of 36,000 U.S. deaths a year now when there were just 34,000 deaths recorded in the 1968-1969 "Hong Kong flu" epidemic? he asked.

But William W. Thompson, the CDC epidemiologist who was the lead author of the 2003 paper, said Doshi is missing the big picture.

The increase in older Americans has been substantial over the longer run -- up by 48 percent between 1976 and 1999, he said. The number of Americans in the most-vulnerable 85-and-older age group has doubled during that time, Thompson said.
That increase in the older population explains why more Americans die in an ordinary flu year nowadays than in the Hong Kong pandemic, he said. Most of them don't die directly of the flu, Thompson stressed. Instead, the immediate cause of death is often listed as pneumonia.

"Influenza is rarely reported on the death certificate, even though influenza is responsible for many deaths," Thompson said. "Pneumonia and influenza are grouped together because many pneumonias result from influenza. Influenza is listed as a secondary cause of death."

That is not how Doshi sees it. Instead, his article talks of a "public relations approach" linked to drug company profits. "CDC is already working in the manufacturers' interest by conducting campaigns to increase vaccinations," he wrote.
"I don't understand that argument," Thompson said. "We have used this method for the past 40 years, and we continue to use these estimates. We don't need drug manufacturers' approval or anything like it."

Thompson said the CDC's annual advice remains the same: "I think that people who are at high risk for flu- associated complications should get vaccinated."
Of the British Medical Journal, he said, "It surprises me that they would publish something like that without giving us a chance to reply."

Will there be a reply?

"We're considering it," Thompson said.

More information
Guidelines for the prevention and treatment of colds and the flu are available at the American Lung Association (www.lungusa.org ).
SOURCES: Peter Doshi, graduate student, Harvard University, Boston; William W. Thompson, Ph.D., epidemiologist, U.S. Centers for Disease Control and Prevention, Atlanta; Dec. 10, 2005, British Medical Journal



http://bmj.bmjjournals.com/cgi/content/full/331/7529/1412

Are US flu death figures more PR than science?

US data on influenza deaths are a mess. The Centers for Disease Control and Prevention (CDC) acknowledges a difference between flu death and flu associated death yet uses the terms interchangeably. Additionally, there are significant statistical incompatibilities between official estimates and national vital statistics data. Compounding these problems is a marketing of fear—a CDC communications strategy in which medical experts "predict dire outcomes" during flu seasons.

The CDC website states what has become commonly accepted and widely reported in the lay and scientific press: annually "about 36 000 [Americans] die from flu" (www.cdc.gov/flu/about/disease.htm) and "influenza/pneumonia" is the seventh leading cause of death in the United States (www.cdc.gov/nchs/fastats/lcod.htm). But why are flu and pneumonia bundled together? Is the relationship so strong or unique to warrant characterising them as a single cause of death?

David Rosenthal, director of Harvard University Health Services, said, "People don't necessarily die, per se, of the [flu] virus—the viraemia. What they die of is a secondary pneumonia. So many of these pneumonias are not viral pneumonias but secondary [pneumonias]." But Dr Rosenthal agreed that the flu/pneumonia relationship was not unique. For instance, a recent study (JAMA 2004;292: 1955-60[Abstract/Free Full Text]) found that stomach acid suppressing drugs are associated with a higher risk of community acquired pneumonia, but such drugs and pneumonia are not compiled as a single statistic.

CDC states that the historic 1968-9 "Hong Kong flu" pandemic killed 34 000 Americans. At the same time, CDC claims 36 000 Americans annually die from flu. What is going on?

Meanwhile, according to the CDC's National Center for Health Statistics (NCHS), "influenza and pneumonia" took 62 034 lives in 2001—61 777 of which were attributed to pneumonia and 257 to flu, and in only 18 cases was flu virus positively identified. Between 1979 and 2002, NCHS data show an average 1348 flu deaths per year (range 257 to 3006).

The NCHS data would be compatible with CDC mortality estimates if about half of the deaths classed by the NCHS as pneumonia were actually flu initiated secondary pneumonias. But the NCHS criteria indicate otherwise: "Cause-of-death statistics are based solely on the underlying cause of death... defined by WHO as `the disease or injury which initiated the train of events leading directly to death.'"
In a written statement, CDC media relations responded to the diverse statistics: "Typically, influenza causes death when the infection leads to severe medical complications." And as most such cases "are never tested for virus infection...CDC considers these [NCHS] figures to be a very substantial undercounting of the true number of deaths from influenza. Therefore, the CDC uses indirect modelling methods to estimate the number of deaths associated with influenza."

CDC's model calculated an average annual 36 155 deaths from influenza associated underlying respiratory and circulatory causes (JAMA 2003;289: 179-86[Abstract/Free Full Text]). Less than a quarter of these (8097) were described as flu or flu associated underlying pneumonia deaths. Thus the much publicised figure of 36 000 is not an estimate of yearly flu deaths, as widely reported in both the lay and scientific press, but an estimate—generated by a model—of flu-associated death.

William Thompson of the CDC's National Immunization Program (NIP), and lead author of the CDC's 2003 JAMA article, explained that "influenza-associated mortality" is "a statistical association between deaths and viral data available." He said that an association does not imply an underlying cause of death: "Based on modelling, we think it's associated. I don't know that we would say that it's the underlying cause of death."

Yet this stance is incompatible with the CDC assertion that the flu kills 36 000 people a year—a misrepresentation that is yet to be publicly corrected.
Before 2003 CDC said that 20 000 influenza-associated deaths occurred each year. The new figure of 36 000 reported in the January 2003 JAMA paper is an estimate of influenza-associated mortality over the 1990s. Keiji Fukuda, a flu researcher and a co-author of the paper, has been quoted as offering two possible causes for this 80% increase: "One is that the number of people older than 65 is growing larger...The second possible reason is the type of virus that predominated in the 1990s [was more virulent]."

However, the 65-plus population grew just 12% between 1990 and 2000. And if flu virus was truly more virulent over the 1990s, one would expect more deaths. But flu deaths recorded by the NCHS were on average 30% lower in the 1990s than the 1980s.
If passed, the Flu Protection Act of 2005 will revamp US flu vaccine policy. The legislation will require CDC to pay makers for vaccines unsold "through routine market mechanisms." The bill will also require CDC to conduct a "public awareness campaign" emphasising "the safety and benefit of recommended vaccines for the public good."

Yet this bill obscures the fact that CDC is already working in manufacturers' interest by conducting campaigns to increase flu vaccination. At the 2004 "National Influenza Vaccine Summit," co-sponsored by CDC and the American Medical Association, Glen Nowak, associate director for communications at the NIP, spoke on using the media to boost demand for the vaccine. One step of a "Seven-Step `Recipe' for Generating Interest in, and Demand for, Flu (or any other) Vaccination" occurs when "medical experts and public health authorities publicly...state concern and alarm (and predict dire outcomes)—and urge influenza vaccination" (www.ama-assn.org/ama1/pub/upload/mm/36/2004_flu_nowak.pdf). Another step entails "continued reports...that influenza is causing severe illness and/or affecting lots of people, helping foster the perception that many people are susceptible to a bad case of influenza."

Preceding the summit, demand had been low early into the 2003 flu season. "At that point, the manufacturers were telling us that they weren't receiving a lot of orders for vaccine for use in November or even December," recalled Dr Nowak on National Public Radio. "It really did look like we needed to do something to encourage people to get a flu shot."

If flu is in fact not a major cause of death, this public relations approach is surely exaggerated. Moreover, by arbitrarily linking flu with pneumonia, current data are statistically biased. Until corrected and until unbiased statistics are developed, the chances for sound discussion and public health policy are limited.
Peter Doshi, graduate student Harvard University pdoshi@fas.harvard.edu

October 25, 2005

WaPo: Flu Death Risk Often Exaggerated; So Is Benefit of Vaccine

A Shot of Fear
Flu Death Risk Often Exaggerated; So Is Benefit of Vaccine

By Steven Woloshin, Lisa M. Schwartz and H. Gilbert Welch
Special to The Washington Post
Tuesday, October 25, 2005; Page HE01

Medical research often becomes news. But sometimes the news is made to appear more definitive and dramatic than the research warrants. This series dissects health news to highlight some common study interpretation problems we see as physician-researchers and show how the research community, medical journals and the media can do better.

For years, the public health community has used fear as one strategy to promote the flu vaccine. A vaccination poster distributed by the U.S. Centers for Disease Control and Prevention (CDC), for example, emphasizes that "36,000 Americans die of flu-related illnesses each year," implying that the vaccine could prevent many of these deaths.

What was an elderly person's chance of having a flu-like illness in a flu season?
Placebo group Vaccine group
Nursing Home
Study 1 (Russia) 13% 5%
Study 2 (U.S.) 15% 6%
Community
Study 3 (Netherlands) 4% 2%
Study 4 (Britain) 9% 5%
Study 5 (U.S.) 4% 2%
SOURCES: Lancet Online Cochrane Review 2005 and original journal articles

When it became aware of the vaccine shortage last October, the federal government changed course and tried to reassure Americans that going without a shot was no big deal. "We all need to take a deep breath. This is not an emergency," CDC director Julie Gerberding advised the public.

Instead of urging vaccination for everyone age 50 and older, as they had been doing, government officials recommended shots only for people 65 and older, and those in selected high risk groups. The public's response was predictable: People were upset and confused. Our local television news played a story in which a pharmacist was called "a murderer" when his vaccine supply ran out. Ironically, the crisis mentality led some to engage in behaviors that probably increased their risk. Frail elderly people, some with oxygen tanks, stood in long lines in the cold, waiting for the vaccine. Others crowded clinics and doctors' offices, increasing their chance of exposure to flu and other infectious agents.

With uncertainties about this year's vaccine supply, the CDC again recommended that highest-risk people get priority for flu shots, at least until late October. But last year's flu season may have left people confused about essential points: Just how risky is the flu? And just how effective is the vaccine? The answers to these questions may surprise readers.

How Risky Is the Flu?

First, a caveat: The risk calculations we analyze here describe typical flu seasons only. We don't consider here what the picture would be in the event of a deadly flu pandemic -- a worldwide outbreak of a new, highly virulent flu strain, the potential for which has recently drawn considerable media attention. No one really knows how likely such an outbreak is, but the risk profile would certainly change. A pandemic is a fundamentally different situation: The risk of death would be substantially higher, and untested strategies (including new treatments, quarantine and a new vaccine) would need to be implemented rapidly.

We deal here with what is known about typical flu seasons, based on data that form the basis for the federal government's flu-risk figures.

By choosing to highlight the annual number of flu deaths, the CDC employed an attention-grabbing tactic often used by public health and disease advocacy groups. It's a tactic readers should be inoculated against if they want a clear picture of the risks they face. (See "Research Basics: Understanding How Big a Risk Is," right.)

In fact, it is very difficult to know how many people die from any given disease because there is often much uncertainty in determining the cause of death. This is particularly true for the flu. That's because it shares symptoms with so many other diseases, and because people most likely to die a flu-related death are also at high risk for many other causes of death.

Flu deaths are probably undercounted because doctors do not routinely test for the flu, and because some deaths that should be attributed to the flu are given other diagnoses. For example, someone who dies from a heart attack because they are debilitated by the flu might not get counted as a flu death. Some overcounting of flu deaths also occurs: Clearly not all winter pneumonia deaths are caused by the flu.

According to the CDC, 90 percent of flu-related deaths occur among people age 65 years and older. Based on this information and the age distribution of the population, the chance of a flu-related death for people in that age group is about one in 1,000. Another way of saying this is that the chance of not dying from flu for those 65 and older is about 999 out of 1,000. (For context, the chance of a flu-related death is slightly lower than the chance of dying from a fall or other accident.)

For people younger than 65 (including children), the chance of a flu-related death is much smaller -- about one in 100,000. Of course, adults and children might be concerned about flu-related problems besides death, such as being hospitalized or just suffering with unpleasant symptoms (typically three to seven days of fever, muscle aches, headache, weakness, dry cough and runny nose). As you might guess, counting the number of flu-related hospitalizations or the number of people experiencing symptoms from the flu is even more difficult than counting flu deaths.

How Good Is the Vaccine?

Getting a shot does not guarantee you will not get sick from the flu or die from it. Recently, the Cochrane Collaboration, an international group that evaluates the evidence for various medical interventions, reviewed the medical literature on the effectiveness of the flu vaccine in preventing death.

Unfortunately, the evidence on how well the vaccine works to prevent death in the elderly is limited. Few of the existing studies are randomized trials -- considered the gold standard for medical evidence. Instead, most data are from observational studies -- studies in which scientists simply count up outcomes (here, the number of deaths that occur among people who did or did not get the vaccine).

But drawing conclusions about cause and effect from such observations is fraught with problems.

For example, a 2003 study published in the New England Journal of Medicine observed that the flu vaccine was associated with a 50 percent reduction in the overall death rate (that is, death from heart disease, stroke, cancer and all other causes combined). To attribute an effect of this magnitude solely to the flu vaccine is ludicrous: Flu-related deaths make up less than 2 percent of all deaths. If the claim were accurate, the vaccine's power would dwarf that of any other medical intervention. There is, however, a much more likely explanation: People who choose to get a flu shot are much healthier -- and therefore already at much lower risk of death -- than people who do not.

Only five randomized trials have examined the effectiveness of the flu vaccine. In these studies, patients were randomly assigned -- a selection technique equivalent to the flip of a coin -- to get either a flu vaccine or a placebo injection. But none of these studies looked at whether the vaccine prevents death. Instead, the scientists measured who developed a flu-like illness. For a summary of the findings of these studies, see "How Well Does the Vaccine Work in the Elderly?" below.

In the absence of good randomized trial data, it is still possible to gauge the effectiveness of vaccination by looking at time trends in flu vaccine rates compared with flu-related deaths in the elderly. As more people get vaccinated, you would expect the flu-related death rate to decline -- if the vaccine is effective. But, as the graph below, titled "A Windening Gap," shows, despite a dramatic increase in vaccination among the elderly, deaths from the flu and pneumonia have hardly budged. (The calculations have taken into account the aging of the population.)

For younger adults, flu-related death is so rare that it has not been reliably studied: Doing so would require a trial of millions of people.

Of course, the flu shot may have benefits besides reducing the chance of death. Many may get flu shots simply to avoid getting sick. The Cochrane Collaboration identified more than 20 randomized trials addressing this question. The overall chance of developing "clinical" flu (we'll explain in a minute) was 19 percent in those chosen, again by chance, to receive the recommended flu vaccine vs. 23 percent in the control groups.

The careful reader may notice that these percentages are substantially higher than those reported for the elderly. (See "How Well Does the Vaccine Work in the Elderly?") This is because clinical flu is defined as a set of non-specific symptoms including fever, cough and muscle aches -- symptoms shared by many non-flu illnesses like the common cold. These non-flu illnesses may be especially common in younger adults because of their exposure to other people, particularly children. To try to isolate the effect of the vaccine, scientists sometimes use laboratory tests to confirm the activity of flu virus in the blood. Using this measure, the chance of flu in the vaccine group is 2 percent vs. 7 percent in the control group.

Studies have also measured another outcome: how vaccination affects days lost from work. On average, there are about 0.16 fewer days lost from work per person vaccinated. Another way of saying this is that about 5 percent of those vaccinated avoid missing about three days of work because of the flu. (That is, 0.16 days divided by the 5 percent who benefited from vaccination equals 3.2 days.) The other 95 percent vaccinated got no benefit.

Take-Home Messages

To promote vaccine use, many in the public health community have overstated the risk of flu-related death and the effectiveness of the vaccine in preventing it. While the flu vaccine may have some important benefit (less flu-related illness), we really do not know whether it reduces the risk of death. For younger individuals -- for whom the chance of flu-related death is extremely small -- any death-protection benefit can only be very modest (and it is unlikely we will ever reliably know whether it even exists). However, we do know that the vaccine reduces the risk of being sick and time lost from work. But because the effect is small, individuals will have to judge for themselves whether it's worth the bother.

We are not suggesting that Americans forgo flu vaccines. We simply want to help people make informed decisions.

For many people, getting the vaccine is a reasonable choice. And many may reasonably choose not to get it. (Consequently, the use of flu vaccination rates by Medicare and others to measure health care quality probably does not make sense.)

Regardless, public health officials should not exaggerate risks or benefits to promote vaccination. Exaggeration carries a price: Not only do some people get scared and engage in behaviors that increase their risk (like waiting in a crowded clinic for a flu shot). They may also grow cynical and end up ignoring health messages that really matter.

Steven Woloshin, Lisa Schwartz and Gilbert Welch are physician-researchers in the VA Outcomes Group in White River Junction, Vt., and faculty members at the Dartmouth Medical School. They conduct regular seminars on how to interpret medical studies. (Seehttp://www.vaoutcomes.org.) The views expressed do not necessarily represent the views of the Department of Veterans Affairs or the United States Government.

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