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GPs are preparing to alert patients they’re eligible for a coronavirus booster shot as pharmacists call for access to the Pfizer vaccine, with a decision on Pfizer boosters expected before the end of the week.
The Therapeutic Goods Administration’s vaccine advisory committee met on Monday to consider the use of Pfizer’s COVID-19 jab as a booster. The Australian Technical Advisory Group on Immunisation will then consider the benefits of a broad booster program later this week.
“We expect to receive advice from the Therapeutic Goods Administration and ATAGI within the coming days about the administration of booster doses for the general population,” a spokeswoman from the Department of Health said on Monday.
Health Minister Greg Hunt said last week the government was ready to roll out a booster program once it is approved by the medical bodies, and Deputy Chief Medical Officer Professor Michael Kidd said the Commonwealth was preparing to start a rollout on November 8.
The evidence for boosters is not clear-cut, however, with scientists fiercely debating whether they are really needed at all.
Royal Australian College of General Practitioners president Dr Karen Price expects most GP clinics will use their normal patient recall system, which in many cases includes text messages, to alert patients as they become eligible for the booster.
“We are looking forward to getting on with that,” she said.
Pharmacists are also keen to be involved in the booster rollout, but currently risk being left out unless the federal government allows pharmacists to dispense Pfizer doses, or unless Moderna applies for its vaccine to be used as a booster. Moderna is expected to submit data for consideration soon.
If you want the information, go look for it. By searching “Intellectual Property” in the search bar on the top right of Moderna’s website, you can find the patent information pertaining to the vaccine. Press CTRL F, and search lucifer. Here we have luciferase. Upon research you’ll find that the enzyme “luciferase” produces bioluminescence. Well, we all know what the highest esteemed freemasons have to say about lucifer being light. We have the CHOICE to dive into the research and to see through satans illusion. Stay inquisitive in the word of God, and the world around you.
Source: TheAge, ModernaPatent
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This week’s U.S. data for 12- to 17-year-olds show:
21,921 total adverse events, including 1,325 rated as serious and 25 reported deaths. Two of the 25 deaths were suicides.
The most recent death involves a 12-year-old girl (VAERS I.D. 1784945) who died from a respiratory tract hemorrhage 22 days after receiving her first dose of Pfizer’s vaccine.
Another recent death includes a 15-year-old male who died six days after receiving his first dose of Pfizer’s COVID vaccine. According to his VAERS report (VAERS I.D. 1764974), the previously healthy teen complained of brief unilateral shoulder pain five days after receiving his COVID vaccine.
The next day he played with two friends at a community pond, swung on a rope swing, flipped into the air, and landed in the water feet first. He surfaced, laughed and told his friends “Wow, that hurt!” He then swam toward shore underwater, as was his usual routine, but did not re-emerge.
An autopsy showed no external indication of a head injury, but there was a small subgaleal hemorrhage — a rare, but lethal bleeding disorder — over the left occiput. In addition, the boy had a mildly elevated cardiac mass, increased left ventricular wall thickness and small foci of myocardial inflammation of the lateral wall of the left ventricle with myocyte necrosis consistent with myocardial infarction.
57 reports of anaphylaxis among 12- to 17-year-olds where the reaction was life-threatening, required treatment or resulted in death — with 96% of cases attributed to Pfizer’s vaccine.
535 reports of myocarditis and pericarditis (heart inflammation) with 527 cases attributed to Pfizer’s vaccine.
119 reports of blood clotting disorders, with all cases attributed to Pfizer.
Demons speaking through a Greek Roman Catholic priest said there will be 7 shots all together.
Young mother pressured to receive COVID vaccine dies of vaccine-induced blood clots
Jessica Berg Wilson, a 37-year-old stay-at-home mother from Washington passed away suddenly on Sept. 7 from vaccine-induced thrombotic thrombocytopenia (VITT) — a rare, and sometimes fatal, blood-clotting condition — after receiving J&J’s COVID vaccine. On Aug. 29, Jessica went to a Seattle pharmacy to get her COVID vaccine and was told she would be receiving J&J’s shot. She was “vehemently opposed” to taking the vaccine, “considering her stay-at-home mom status, state of good health and young age in conjunction with the known and unknown risk of an unproven vaccine,” her husband said.
But Jessica was pressured to get the vaccine due to a vaccine mandate at their child’s school requiring “room moms” who wished to serve in the classroom be fully vaccinated.
According to Jessica’s VAERS report (VAERS I.D. 1683324), she experienced blood clots in her ovarian and renal veins, and a brain hemorrhage that led to tissue damage. Although doctors tried to relieve the pressure on her brain by performing a craniotomy, they were unsuccessful.
Jessica was ultimately pronounced brain dead, removed from life support and passed away. Doctors confirmed the cause of death was VITT.