MANILLA — Philippines President Rodrigo Duterte created controversy this week. He reportedly received the first dose of the China-manufactured Sinopharm “inactivated virus” COVID-19 shot this past Monday night. He broadcast the injection live on Facebook. The problem is that only the China-manufactured “inactivated virus” Sinovac Coronavac and Oxford-AstraZeneca viral vector shots are authorized for emergency use in the country. Duterte issued a public apology after being criticized for what looks like avoidance of the shots that every other Filipino is forced or chooses to receive. The optics look even worse now that deaths and adverse reactions are piling up for the “authorized” shots. At least 24 deaths and 24,698 adverse reactions to experimental injections have been reported to government officials since the March rollout, according to ABS-CBN in Quezon City. AstraZeneca is responsible for 14 of the deaths. Sinovac is responsible for 10 deaths. The Philippines Food and Drug Administration (FDA) went into subterfuge mode from there.
The U.K. Government have released the sixth update highlighting adverse reactions to the Pfizer / BioNTech MRNA vaccine and the Oxford / AstraZeneca Viral Vectored vaccine, which have both been authorised for emergency use only in the United Kingdom, and the rate of adverse reactions has increased… again.
Some highlights if we could call them that! So much happening & catching up here with just a sprinkling of latest developments. Stay safe and informed. Research! EWR
From Children’s Health Defense:
From Health Impact News
From Dr Mercola
“SWITZERLAND has made a shock move not to approve the Oxford/AstraZeneca vaccine for use in its roll out of Covid jabs.
…. a growing list of EU countries refusing to allow the use of the vaccine in older people.”
I noted the other day mainstream saying that in NZ children will not be injected (yet) with this experimental vaccine that has only been approved for emergency use. Last November it was said they’d be first. So we have in this UK article 300 children aged 6-17 to be injected in trials of the Oxford/AstraZeneca vax when clearly from the evidence there are side effects, some very serious ones. (They have skipped the animal testing because the vaccine was developed in less than twelve months… a process that can normally take from 7-10 years.. video at 4min.56). These are documented on the data bases. (See here also re true numbers). My question is, how does one obtain a 6 YO volunteer? We cannot vote until 16+ allowing variations for different countries. One can only assume that the parent who has legal authority over the child is giving their consent to volunteer their child. Have those parents been given the full disclosure of possible side effects? One would hope so. Who is even stopping amidst this frenzy to even look at those?
Read at the link below