Right from the CDC website:

 The ACIP uses VAERS reports to determine the safety of Vaccines:

http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6041a4.htm 

 Safety of Tdap in Pregnant Women

In prelicensure evaluations, the safety of administering a booster dose of Tdap to pregnant women was not studied. Because information on use of Tdap in pregnant women was lacking, both manufacturers of Tdap established pregnancy registries to collect information and pregnancy outcomes from pregnant women vaccinated with Tdap. Data on the safety of administering Tdap to pregnant women are now available.

ACIP reviewed published and unpublished data from VAERS,

Sanofi Pasteur (Adacel) and GlaxoSmithKline (Boostrix) pregnancy registries, and small studies (7,8). ACIP concluded that available data from these studies did not suggest any elevated frequency or unusual patterns of adverse events in pregnant women who received Tdap and that the few serious adverse events reported were unlikely to have been caused by the vaccine. Both tetanus and diphtheria toxoids (Td) and tetanus toxoid vaccines have been used extensively in pregnant women worldwide to prevent neonatal tetanus. Tetanus- and diphtheria-toxoid containing vaccines administered during pregnancy have not been shown to be teratogenic (9,10). From a safety perspective, ACIP concluded that administration of Tdap after 20 weeks' gestation is preferred to minimize the risk for any low-frequency adverse event and the possibility that any spurious association might appear causative.

The Most Recent Recomendation for the Flu Shot in the 2012 Season includes investigation of VAERS reports for any allergic reactions to eggs.

 Recent examination of VAERS data indicated no disproportionate reporting of allergy or anaphylaxis after influenza vaccination during the 2011–12 season (21). For the 2012–13 influenza season, ACIP recommends the following:

1. Persons with a history of egg allergy who have experienced only hives after exposure to egg should receive influenza vaccine, with the following additional safety measures (Figure 2):

 http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6132a3.htm

What is the ACIP?  Experts in the following areas:

he ACIP nominally contains fifteen regular members, each an expert in one of the following fields:^[5]

• immunization practices and public health
• use of vaccines and other immunobiologic agents in clinical practice or preventive medicine
• clinical or laboratory vaccine research
• assessment of vaccine efficacy and safety
• consumer perspectives and/or social and community aspects of immunization programs; at least one member must be an expert in this category.

In addition, the ACIP includes ex-officio members from Federal agencies involved with vaccine issues, and non-voting liaison representatives from medical and professional societies and organizations.^[7]

http://en.wikipedia.org/wiki/Advisory_Committee_on_Immunization_Practices

http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6041a4.htm

There have been reports from epidemiological studies confirming suspicions that those who are vaccinated often don't do as well with long-term health as those who are vaccination free.

Those epidemiological studies (statistical surveys) have shown that bad health is more common among the vaccinated who survive without serious injury than children not vaccinated.

But how and why has not come under controlled animal lab studies until Japan's Kobe University animal lab study of 2009.

This study was reported and peer reviewed in the PLOS One Open Journal at the end of 2009, but has not received much if any public attention. It was brought to public's attention very recently by homoeopathist and health writer Heidi Stevenson's article on her Gaia Health blog. (Source below)
 

Japanese study summary

Here's the conclusion quoted from the

study's journal report:

"Systemic autoimmunity appears to be the

of over-stimulating the host's immune 'system' by repeated immunization with antigen, to the levels that surpass system's self-organize criticality." (Emphasis added.)

The initial purpose of this independently funded study was to understand how autoimmune diseases develop from autoimmunity. It was not an effort to prove vaccination safety or danger.

The researchers used mice that were bred to avoid autoimmune diseases and injected them with solutions that contain antigens. Antigens generate antibodies to protect against invading disease pathogens. Antibodies can turn against the host if they become self generated, causing autoimmune diseases.

A

injects cultured vaccine antigens of weakened or dead viruses to create an immune response of antibodies to that antigen, supposedly for creating immunity to that particular disease.

It's not very unusual for cytokine storms (

overreactions) to overwhelm one who has been vaccinated. Vaccine adverse reactions have caused injuries of permanent disability, autism spectrum disorders, or death more often than publicly disclosed.

The Kobe researchers injected the mice that were bred to not develop autoimmune diseases repeatedly with antigens, much like vaccinations are administered to infants and children, to

how an immune system could turn on itself to create autoimmune diseases.

They were pushing the mice's immune systems to see if and when they would no longer bend, but break. They used

(SEB) as their injected antigens.

such as mercury, aluminum, or formaldehyde used in vaccines. Antigens were used without the toxic additives normally used in vaccinations.

After seven injections the mice recovered each time with their immune systems intact. But after the eighth injection, problems with key immunity cells began arising.

Damaged cells were observed microscopically and showed signs of early autoimmunity. Their immune systems had started to self generate antibodies for autoimmune reactions after repeated antigen inoculations. (Source below)

Conclusion

This study should put to rest the notion that "greening" vaccines, that is removing or withholding vaccines' normal toxic additives, would make the childhood vaccination schedule of close to 40 vaccinations by 18 months of age more agreeable.

The Kobe animal trials demonstrated how autoimmune reactions were created as a consequence of repeated antigen

inoculations with long enough breaks between each injection to allow complete recoveries.

Autoimmune diseases have increased in quantity and variety as childhood vaccination schedules increased and more vaccines were made available for naive recipients. Even infectious diseases that vaccines are supposed to immunize against have appeared among the vaccinated more often than publicly admitted.

The very basis of creating immunity with even "greened" vaccinations is worse than false, it is actually unhealthy.

Heidi's article:

The Japanese study's journal report:

Antigens explained:

Recommended vaccination schedule for children to age six:

You left out:

Feeble atempts by mainstream apologists which have been thoroughly discredited and beaten back time after time.