You're saying that 10's of thousands of people have NOT died due to the vax, correct?Because that hasn't happened.
You're saying that 10's of thousands of people have NOT died due to the vax, correct?Because that hasn't happened.
100% are dead with out.Vents are counterproductive.
75% of vent parients are dead.
You're saying that 10's of thousands of people have NOT died due to the vax, correct?
i'll have to read the study, but that's a pathetic excuse for journalism...even for the LA Times.
Not a double negative. It’s a statement that it doesn’t do jackshit. “Jackshit” is a very low threshold, but a tad more than zero. Ivermectin purported benefits don’t rise to the level of jackshit.Double negative in title so it actually do something
Because you respect your very, very, very, very, very.....very elders.Not a double negative. It’s a statement that it doesn’t do jackshit. “Jackshit” is a very low threshold, but a tad more than zero. Ivermectin purported benefits don’t rise to the level of jackshit.
WTF am I wasting my time trying to explain this to a 90 year old?
sounds like covid to meI was under the influence when I typed that. I had taken MDMA mixed with fentanyl and heroin.
Lol, that's not true!100% are dead with out.
With a po2 40 and a PCO2 of 90 and tachypneic at 35, Should I just sit there and watch them guppy until they die?
What you missed out on the ventilator conversation is two distinct phenotypes of ventilation perfusion compromise in covid. You've only memorized that there are a portion that risk baro trauma following ardsnet protocols. You've forgotten that there's a whole other that are proper ARDS.
And in both cases you're dead without the vent. It's just two different ventilator strategies.
WAT?so come correct with something new besides VAERS
For the record, @sparkuri has probably never run the numbers of Eudravigilence on the vaccines himself.Eudraviligence
Stylin on em.100% are dead with out.
With a po2 40 and a PCO2 of 90 and tachypneic at 35, Should I just sit there and watch them guppy until they die?
What you missed out on the ventilator conversation is two distinct phenotypes of ventilation perfusion compromise in covid. You've only memorized that there are a portion that risk baro trauma following ardsnet protocols. You've forgotten that there's a whole other that are proper ARDS.
And in both cases you're dead without the vent. It's just two different ventilator strategies.
Does that lady have a meta-analysis?
If she's an expert at studies review and guideline creation, does she have a review printed that has proper inclusion and exclusion criteria to help cut through "the noise" referenced?
Ivermectin for Prevention and Treatment of COVID-19 Infection: A Systematic Review, Meta-analysis, and Trial Sequential Analysis to Inform Clinical Guidelines - PubMed
Moderate-certainty evidence finds that large reductions in COVID-19 deaths are possible using ivermectin. Using ivermectin early in the clinical course may reduce numbers progressing to severe disease. The apparent safety and low cost suggest that ivermectin is likely to have a significant...pubmed.ncbi.nlm.nih.gov
She is Theresa Lawrie
Have u doe?!?For the record, @sparkuri has probably never run the numbers of Eudravigilence on the vaccines himself.
He however posted a link to a questionable source claiming to have run em, and he even quoted that source incorrectly on here by claiming the total amount of adverse effects (so mild included) as serious cases, when in fact serious cases are a distinct and different number.
He can't read my post so it's just for info for anyone taking his numbers into account.
The key at this point is keeping patients out of the hospital by starting treatment early in disease progression. If vaccination rates are going to remain subpar (which is a certainty due to the insanity that they have somehow become politicized and public health statements get bastardized by narratives), then earlier treatment needs to be the focus.
Monoclonal antibodies (mAb) are severely underutilized right now. Early studies looked at their efficacy in progressive stages of disease, where they didn’t fare so well. When studies looked at their ability to prevent that disease progression and keep people out of the hospital, they performed tremendously. The Lilly product was pulled from its EUA (emergency use authorization) but the Regeneron and GlaxoSmithKline options are faring very well against the currently most common variants, including Delta. Due to the guardrails of my position, I can’t get into some of the confidential details about what is to come, but I can say that there will be new presentations of the mAbs which will make administration and site of care more efficient. Also, with the emerging variants that will inevitably make up a higher percentage of cases in the coming months/year, there will be further differentiation within the available mAbs as far as efficacy, but the good news is there will be at least one option that shows efficacy against the next few which are most likely to emerge (at least in the US. There will continue to be variability in rates/variant globally).
Hard "R"?
Yes, about two months ago for one vaccine (the one I was going to get).Have u doe?!?
U never did a science thing in ur life bruv!Yes, about two months ago for one vaccine (the one I was going to get).
But it's a lot of work and you have to take it with a grain of salt as well since none of the data is vetted, and only about half is actually reported by medical personnel.
And ofc the numbers are ever-changing, so two months ago doesn't mean much now.
It's the "I-word".