Excerpts:
The New Pneumonia Jab
PREVNAR VACCINE (FOR PNEUMONIA AND PNEUMOCOCCAL MENINGITIS)
SIDE-EFFECTS:
50% of recipients will get redness and soreness at the injection site, 21% get a fever (over 100.3 F), chills, general malaise, irritability, drowsiness, decreased appetite, arthritis. 1 in 10,000 cases involves a serious reaction including trouble breathing, hives, having a fast heartbeat and becoming dizzy.
Seizures also occurred in 1 in 10,000 – almost all seizures occurred within 4 days of vaccination. (2 and 3).
According to the manufacturer, Wyeth, the following reactions may also occur:
Vomiting, diarrhoea, injection site redness, fever over 38 Degrees C, drowsiness, irritability, swelling interfering with movement, seizures, hypotonic hyperesponsive episode, dermatitis, face oedema, angioneurotic oedema, dyspnoea, bronchospasm, anaphylactic shock.
As with other aluminium-containing vaccines, a nodule may occasionally be palpable at the injection site for several weeks
As the rate for pneumonia is 10 in 100,000 and the rate for serious vaccine side-effects is
1 in 10,000, this makes the risk from the vaccine the same, if not more, than the risk from the disease.
SAFETY TRIAL
Of the 17,066 children involved in the Prevnar safety trial, there were 24 hospitalisations, including 2 cases of pneumonia and 1 case of otitis media (the very things they are supposed to be immunising against) and 1 case of congestive heart failure. In addition to this there were also 162 visits to the emergency room department including 20 cases of seizure, 15 cases of otitis media, 6 cases of pneumonia and 1 case of sepsis.
12 cases of SIDS death also occurred in subjects receiving Prevnar and 1 SIDS like death in a child over 1 year old. This included 1 death within 1 week of vaccination, 2 deaths 2 weeks after vaccination, 2 deaths one month after vaccination and 4 deaths in the year following vaccination. (4).
There have also been 217 DEATHS reported to Vaccine Adverse Events Reporting System in the US since 2000.
E.G. VAERS case number 167703 states: ‘Information has been received from an investigator regarding a 3 month old female who received her first dose of Prevnar as part of a post-marketing safety surveillance trial. At 39 days, post vax, the infant died due to Sudden Infant Death Syndrome.’ (5). .................information continued at link
Prevnar vaccine is having an unfortunate effect: promoting new superbugs that cause ear infections.