Gilead is accused of ‘downplaying or omitting altogether the clinical dangers experienced by patients from remdesivir use.’
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Deborah Fust, the surviving spouse of Michael Fust, and Edward Pimentel, who says he was injured after receiving remdesivir, are accusing California-based Gilead of failing to mention documented side effects in its promotion of remdesivir.
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The new suit comes after a court in Michigan ruled that remdesivir was not protected under federal law against an action brought by a man who needed his leg amputated after receiving remdesivir.
COMPLAINT FOR DAMAGES AND INJUNCTIVE RELIEF
1. Violations of the Consumers Legal Remedies Act Cal. Civ. Code §§ 1750 et seq.
2. Violations of the False Advertising Law Cal. Bus. & Prof. Code §§ 17500 et seq
3. Violations of the Unfair Competition Law Cal. Bus. & Prof. Code §§ 17200 et seq
4. Money Had and Received.
5. Negligent Misrepresentation.
6. Unjust Enrichment
My name is Jamie Scher, and I am one of the lawyers who filed the Class Action In Shasta County California against Gilead Sciences, Inc., maker of the lethal drug known as Remdesivir and/or Veklury. In case you don’t get through this entire Substack article, let me emphasize the most important point that I would like to make to everyone: DO NOT EVER TAKE THESE DRUGS, EVER!
There are links in the article cited above for participating in this case and for contributing to the costs.
A critically important fact about remdesivir is that this drug was studied for Ebola, and the results were so abysmal that the attempted “treatment” was cancelled; remdesivir had zero benefits, and greatly increased mortality just like the other “Safe and Effective” offerings. Dr. Fauci and his partners-in-crime knew about remdesivir’s safety profile, or lack thereof, and they absolutely knew that it would do nothing against PSYOP-19, but would result in renal failure which would then look a lot like C19 pneumonia, especially when combined with intubation; in other words, they always knew that they were murdering people.
All of these sociopaths must be rounded up, and given speedy trials.
They want you dead.
Do NOT comply.
— 2nd Smartest Guy in the World
Sources:
https://www.documentcloud.org/documents/23994749-class-action-complaint-against-gilead-over-remdesivir.
Cloud Document.
https://www.theepochtimes.com/article/class-action-lawsuit-filed-against-remdesivir-manufacturer-over-alleged-deceptive-practices-5500317.
News.
https://www.2ndsmartestguyintheworld.com/p/class-action-lawsuit-filed-against.
Blog.
https://www.2ndsmartestguyintheworld.com/p/exclusive-lawyer-update-class-action.
Blog.
Related:
https://doi.org/10.1056/NEJMoa1910993.
Research Journal.
ZMapp and Remdesivir were eliminated from the study following an interim analysis during the trial for mortality reasons. Remdesivir was the most dangerous drug in that trial. This trial did not include a control. This trial was funded by NIAID.
https://doi.org/10.1056/NEJMoa2007016.
Research Journal.
31% of patients had serious adverse events. (23% + 8%) The most common serious adverse events — multiple-organ-dysfunction syndrome, septic shock, acute kidney injury, and hypotension — were reported in patients who were receiving invasive ventilation at baseline.
https://doi.org/10.1016/j.ijid.2020.06.093.
Research Journal.
Four of the trial patients had to be removed from the trial early: two because they were heading toward liver failure, and two because they had such severe kidney failure they they required transplants. Two of the trial patients ultimately died. France decided that Remdesivir was too dangerous to use in their country.
https://doi.org/10.1002/cpt.2145.
Research Journal.
See also, on this site: