Remdesivir is a highly toxic drug that medical officials advocate in the fight against Covid, but what is it and why do the same officials ferociously defend it when there are  known side effects that are deadly?  

The FDA approved it under the name Veklury for IVs in non-hospitalised outpatient treatment on January 27th 2022. They also terminated approval of two monoclonal antibody drugs, saying they “didn’t work” on the Omicron variant.

Those two drugs had known life-extending properties for Covid patients. Lets have a look at the controversy and why there maybe more to this than meets the eye. Failed drug.

Remdesivir was developed in 2009 by Gilead Sciences to treat Hepatitis C and respiratory syncytial virus (RSV), but it didn’t work against those diseases. So they “repurposed” it  for the Marburg and Ebola viruses in 2014. It wasn’t effective in stopping the replication in those viruses either and when several people died from it, it was pulled from the trial.

Now it has once again been “repurposed” for the Covid virus, but the narrative NIH that it does stop the SARS-Cov-2 virus. It has not been recommended for Covid patients, but that hasn’t stopped the powers that be.

The side effects of Remdesivir are exactly the same as the symptoms we are being told for Covid. Once a patient in the US  entered hospital  and was put on Remdesivir, they died and the death was put down as Covid.

The European Medicines Agency’s (EMA’s) safety committee is to review reports of acute kidney injury (AKI) in some patients being given remdesivir for COVID-19.

At the same time, a benefit–risk analysis carried out by the UK’s Drug Safety Research Unit (DSRU) has highlighted “limited” safety data available on remdesivir and found it was “unclear” whether reports of serious adverse events, including AKI, were caused by COVID-19 or remdesivir.

 

 

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