2017:
FDA "under pressure from Trump admin to approve drugs faster, but researchers at Yale School of Medicine found nearly 1/3 of those approved from 2001 through 2010 had major safety issues yrs after medications were made widely available to patients."
"Seventy-one of the 222 drugs approved in the 1st decade of the millennium were withdrawn, required a "black box" warning on side effects or warranted a safety announcement about new risks".
This was reported in JAMA in 2017, & the study included safety actions through Feb. 28.
"took a median of 4.2 years after drugs were approved for these safety concerns to come to light, study found, & issues were more common among psychiatric drugs, biologic drugs, drugs that were granted "accelerated approval" & drugs that were approved near regulatory deadline".
"All too often, patients & clinicians mistakenly view FDA approval as indication that product is fully safe & effective...Nothing could be further from the truth. We learn tremendous amounts about a product only once it's on the market & only after use among a broad population."
Note it talks about biologics...
😱This is why the "daddy" of the vaxxes is still pumping them, as well as the other biologics he got through the FDA...
😳Consumer group Public Citizen's Dir of health research, Michael Carome, MD, said Trump's "preposterous promise" to reduce FDA regulations by 75% to 80% would destroy agency's ability to protect public, resulting in "countless preventable deaths, injuries, & illness across US."
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“All of you, yes, I know you’re vaccinated, you’re the smart ones, but you know there’s people out there who aren’t listening to God & what God wants. You know who they are.”
NY Governor said that “God wants” people to be vaccinated—& that those who disagree are not listening to “organized religion” or “everybody from the Pope on down.”
January 21, 2020, the Wuhan Institute of Virology of the China Academy of Sciences applied for a patent on the use of Gilead Sciences’ experimental US antiviral drug, which scientists think could provide treatment for the coronavirus. reuters.com/article/us-chi…
Patent application submitted jointly w/ Military Medicine Institute of People’s Liberation Army Academy of Military Science & Wuhan Institute of Virology. Paper published 2/4/20 in Nature’s Cell Research found Remdesivir & Chloroquine an effective way to inhibit coronavirus.
2/1/20: Hong Kong Health Dept notifed UK Registered Diamond Princess agent, that man who left ship week earlier tested COVID+. Ship quarantined Okinawa, but passengers not informed for 2 days. Princess continued dancing, gyms, casinos, bars & buffet meals. nhk.or.jp/special/plus/a…
Graph that estimates the day when passengers are infected, which is derived from the data of the day of onset and the incubation period.
Estimated number of passengers infected on board each day From a paper by Professor Hiroshi Nishiura, Graduate School of Hokkaido University
NHK prepared a place that imagined buffet-style restaurant venue on the ship, & conducted an experiment with experts that used fluorescent paint as a virus.
👉2/3/21: FDA reissued letter of EUA authorization to allow flexibility on date of submission of reporting of vaccine administration errors by Pfizer.
How is this legal!
👉8/23/21: FDA clarified subsequent to FDA approval of COMIRNATY (COVID19 Vaccine) for 16 yrs & older, EUA would remain in place for Pfizer-BioNTech Vax.
👉Also authorized COMIRNATY (COVID-19 Vax)
😱which has full FDA APROVAL under this EUA for certain uses!
👉Having concluded revising Comirnaty EUA is appropriate to protect public health or safety FDA again reissuing 10/21/21 letter of authorization in entirety w/ revisions to amend EUA for COMIRNATY Vax & Pfizer-BioNTech Vax to authorize use as a single booster dose 18 yrs or older
328/20: Trump's FDA, under Director Stephen Hahn, gives Emergency Use Authorization for Chloroquine Phosphate or Hydroxychloroquine Sulfate Supplied From Strategic National Stockpile for Treatment of 2019 Coronavirus Disease. Rick Brite of BARDA agreed.
6/15/20: Gary Disbrow, Director, Medical Countermeasure Programs BARDA requested FDA Director Stephen Hahn revoke EUA for chloroquine phosphate & hydroxychloroquine sulfate to be distributed from the Strategic National Stockpile issued on 3/28/20:
6/15/20: FDA alert on pulling EUA, stating based on FDA’s continued review, CQ and HCQ are unlikely to be effective in treating COVID-19 for authorized uses in EUA & claimed there were ongoing serious cardiac adverse events and other serious side effects.