(injecting into pure infant bodies with underdeveloped immune systems this onslaught of toxins?)
FDA Approves 6 in 1 Combo Vaccine for “Babies"
On Dec. 21, 2018, the U.S. Food and Drug Administration (FDA) approved a new combination hexavalent vaccine (Vaxelis) that includes antigens for six different diseases: diphtheria, tetanus, pertussis, hepatitis B, poliomyelitis and invasive haemophilus influenza type B.1
Vaccine manufacturers Sanofi Pasteur and Merck jointly developed Vaxelis, which is approved to be given in three doses to children between six weeks and four years of age but children will have to get a separate dose of DTaP vaccine to complete the primary pertussis vaccine series before age four.
The new combination vaccine is expected to be commercially available in the U.S. in 2020.2
Sanofi provided the antigens for diphtheria, tetanus, pertussis, and poliomyelitis for Vaxelis production and Merck provided antigens for H. influenzae type b and hepatitis B.3
Vaxelis has been approved by government regulators in the European Union since 2016.4
Monovalent vaccines include only one antigen, while multivalent or polyvalent vaccines like Vaxelis include either more than one strain of a microorganism or more than one type of microorganism.
Widely used multivalent vaccines include the live attenuated measles, mumps and rubella vaccine (MMR) and the inactivated diphtheria, tetanus and acellular pertussis vaccines (DTaP for children under age seven and Tdap for older children and adults).
Separate vaccines for measles, mumps, rubella and pertussis are not available in the U.S., while tetanus and diphtheria vaccines are only available as a combination (DT or Td) vaccine.
Drawbacks of Combination Vaccines
Combination vaccines have been created by manufacturers to purportedly reduce the number of shots a child must receive to be in compliance with government recommended childhood vaccine schedules and to simplify ordering, transport and storage of vaccines.5
Drawbacks to the multivalent vaccines include a higher risk of pain and swelling at the injection site and, and for Merck’s MMRV (mumps, measles, rubella, varicella) vaccine in particular, a higher incidence of febrile seizures in children under age four.
The product manufacturer package insert for the new hexavalent vaccine states that Vaxelis is contraindicated in children with a history of severe allergic reaction to any of the ingredients of the vaccine, or to any “other diphtheria toxoid, tetanus toxoid, pertussis-containing vaccine, inactivated poliovirus vaccine, hepatitis B vaccine, or H. influenzae type b vaccine.”
According to the Vaxelis product insert, contraindications include:
- “a history of encephalopathy (coma, decreased levels of consciousness, prolonged seizures) within 7 days of a previous dose of pertussis-containing vaccine, that is not attributable to another cause” and “a history of progressive neurologic disorder, including infantile spasms, uncontrolled epilepsy, or progressive encephalopathy until a treatment regimen has been established and the conditions has stabilized.”
The product insert reports high rates of adverse reactions among children receiving the experimental hexavalent vaccine in clinical trials:
- “Rates of adverse reactions varied by number of doses of Vaxelis received. The solicited adverse reactions 0-5 days following any dose were irritability (≥55 percent), crying (≥45 percent), injection site pain (≥44 percent), somnolence (≥40 percent), injection site erythema (≥25 percent), decreased appetite (≥23 percent), fever ≥38.0°C (≥19 percent), injection site swelling (≥18 percent), and vomiting (≥9 percent).”1
Source : The Vaccine Reaction .org PLEASE READ THE COMMENTS!
See also: FDA Approves VAXELIS Combo Vaccine Despite Infant Mortality:
VAXELIS is the first hexavalent (six vaccines in one) drug to be approved in the U.S. and is being hailed as the solution to the increasing number of injections children receive during physician visits. In their first year of life, children routinely receive over 25 vaccines, some administered just hours after birth. Safety concerns have continued to grow as increasing evidence points to vaccines as a cause of many childhood illnesses and even death. The efficacy of these drugs has been hotly debated, though the CDC states unequivocally that vaccines are both safe and effective.
Unfortunately, the standards for safety testing vaccines are significantly lacking. For starters, vaccinated patients are not tested against an unvaccinated control group, but rather against patients vaccinated with other drugs. New vaccines are routinely tested against confirmed dangerous ones in order to arrive at what appear to be positive outcomes. Without a control group, these studies are incapable of accurately measuring the frequency and causal relationships of the vaccines they study.
The duration of these studies is also much smaller than any other drug seeking FDA approval. While most drug studies last for months or even years, vaccines are only evaluated for a few days or weeks. There’s evidence that the preservatives in these vaccines, like aluminum and mercury, are directly related to the alarming rise in autism diagnoses in America. PLEASE READ FULL ARTICLE AT LINK ABOVE.
What's Behind the Recent Rise in Autism in the US? LiveScience (Please Read Full Article) "Virtually everybody has some level of DDT and PCBs in their body. When the body metabolizes DDT, the chemical breaks down into DDE, Brown said. When a woman is pregnant, the fetus is exposed to even higher levels of these chemicals than the mother is exposed to, "because they kind of get concentrated when they go through the mom's blood to the placenta," he said. "Then, they get into the fetal brain, and they alter fetal brain development." [11 Facts Every Parent Should Know About Their Baby's Brain]” Does this also include GLYPHOSATE? :