- Dec 18, 2012
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What did Trump ever say that makes it HIS fault?
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Politico: “Trump White House exerted pressure on FDA for Covid-19 emergency use authorizations, House report finds”:
“The Trump administration pressured the Food and Drug Administration, including former FDA Commissioner Stephen Hahn,to authorize unproven treatments for Covid-19 and the first Covid-19 vaccines on an accelerated timeline, according to a report released Wednesdayby Democrats on the House Select Subcommittee on the Coronavirus Crisis…..
The…administration…tried to pressure the FDA to authorize the first Covid-19 vaccines ahead of the presidential election. When Hahn testified to the subcommittee in January 2022, he said that White House officials said they would not sign off on emergency use authorization language that required a 60-day safety follow up for late-stage clinical trials. Ultimately, the FDA went ahead with the 60-day follow-up plan without an explicit blessing from the White House, though the White House later cleared it.”
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House Democrat Report Blames Trump for Short-Circuiting COVID Vaccine Safety Trials, as Injury and Death Court Claims Skyrocket
A US House of Representatives committee chaired by Rep. Jim Clyburn (D-SC) is faulting the Trump administration, in its rush to obtain FDA approval, for opposing more safety trials for vaccine cand…
coronanews123.wordpress.com
Politico: “Trump White House exerted pressure on FDA for Covid-19 emergency use authorizations, House report finds”:
“The Trump administration pressured the Food and Drug Administration, including former FDA Commissioner Stephen Hahn,to authorize unproven treatments for Covid-19 and the first Covid-19 vaccines on an accelerated timeline, according to a report released Wednesdayby Democrats on the House Select Subcommittee on the Coronavirus Crisis…..
The…administration…tried to pressure the FDA to authorize the first Covid-19 vaccines ahead of the presidential election. When Hahn testified to the subcommittee in January 2022, he said that White House officials said they would not sign off on emergency use authorization language that required a 60-day safety follow up for late-stage clinical trials. Ultimately, the FDA went ahead with the 60-day follow-up plan without an explicit blessing from the White House, though the White House later cleared it.”
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