Because my newsletters tend to become a series of multiple posts I will start collecting them together into one post anthology-style post. Hopefully, this would make it much easier to share and find for newer subscribers and for anyone who wants to check the backlog.
So over the next few days I will go through and make Newsletters for my posts on Quercetin, Hydroxychloroquine, and the Nasal Passage.
Also, now that Substack allows previews of paid posts I’ll retroactively add in preview sections for those who may be interested.
When it comes to citations, just so that I don’t create separate posts that may be unnecessary for most, I will include citations into these Anthology posts if there is no room in the final newsletter of the series. I’ll also try to better cite in-text citations. I’m realizing my citations may make my writings a bit bland and redundant in nature so I will instead try to incorporate footnotes.
And lastly, any additional newsletters that belong under one of these Anthology series will be added to the appropriate post. That way, it should be easy to reference back and view all the posts together.
Part I: Introduction, Brief History, and Mechanism of Action
This is the first post in the series and sets up the rest of the newsletters down the line. A twitter post lead to a testament by a COVID nurse discussing the ineffectiveness of treatments and the dangers of Remdesivir, leading to the search for evidence of possible toxicity.
Part II: The Remdesivir Evidence Before the Pandemic
Remdesivir hasn’t been around for long, but there still exists some in vitro studies of its efficacy. Many of these promising preliminary results lead to its adoption as a possible therapeutic against Ebola. Unfortunately, both the sparse number of studies and questionable results from clinical trials brought Remdesivir’s effectiveness into question.
Part III-1: Remdesivir in the Age of COVID
We start to examine the studies of Remdesivir against SARS-COV2 specifically. Once again, in vitro studies showed very promising results. However, the first clinical studies showed inconsistent results, although many factors may attribute to differences in results.
Part III-2: Remdesivir in the Age of COVID (Examining the NIH Study)
This post focuses more on the NIH trial (ACCT-1). The interim results of this study was pivotal to Remdesivir’s EUA approval. If we examine the study closely, we will find that the benefits of Remdesivir are highly specific and does not work as a “one size fits all” treatment option.
Part IV: Examining the Toxicity & Concluding Remarks
Here we get to the meat of the concern: is Remdesivir actually toxic? The evidence is inconsistent, and although it may not be conclusive, we can at least predict which groups are likely to suffer adverse reactions. I also provide my last remarks on Remdesivir and summarize all of the accumulated evidence.
Part V: When you blame everything but the drug.
This is a Paid Subscriber post. Instead of engaging in the precautionary principle and attributing possible toxicity to a drug and all aspects of a drug, it appears that there’s a greater interest in blaming adverse reactions on everything but Remdesivir.
Citations:
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Thorough and useful information about remdesivir, especially since safe early protocols with Ivermectin, hydroxychloroquine and monoclonal antibodies are still running into hurdles.