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.
February 4, 2020, letter from Military Medicine Institute of People’s Liberation Army Academy of Military Science & Wuhan Institute of Virology. nature.com/articles/s4142…
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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.
18 patients between ages of 3-16 were taken to Children’s Wisconsin Hospital. They include 3 sets of siblings. 10 children are in pediatric ICU-6 critical, 3 serious, & 1 fair. 8 patients in fair condition are in other units.
Jessalyn Kohnke is fighting for her life. She is in ICU, and lost a kidney, broken pelvic, liver lacerations, lung damage, tachycardia and many blood transfusions.
Jessalyn woke up a little yesterday & managed to say, "just glue me back together".
Tucker & Jackson Sparks. Tucker, age 12, is recovering, but sustained road rash & a fractured skull. He is stable at this time. Jackson, age 8, underwent brain surgery on Sunday evening. Doctors will be testing for brain function & brainstem activity.