[ad_1]
We present you the complete post of the professor published on the social network.
“December 18, 2020 The US Food and Drug Administration in Cambridge, Massachusetts, has granted an emergency authorization for the Moderna vaccine. Shortly thereafter, Lindsey Baden of Brigham and Women’s Hospital in Boston, Massachusetts, Hana El Sahly of Baylor College of Medicine in Houston, Texas, and colleagues published the results of a vaccine study involving more than 30,000 volunteers. Half of the study participants received two doses of placebo and half received two doses. of vaccine with a break of 28 days.
The results of the study showed that the vaccine was effective in preventing the development of symptomatic COVID-19. Symptomatic Covid-19 disease was confirmed in 185 placebo participants (56.5 per 1000 man-years; 95% confidence interval [PI], 48.7–65.3) and 11 participants in the mRNA-1273 vaccine group (3.3 / 1000 people). All 30 study participants who developed a severe course of COVID-19 were in the placebo group. Serious adverse events were rare and the incidence was similar in both groups.
Europe is awaiting the decisions of the EMA and the European Commission. A vaccine from Pfizer will not solve all problems. According to European media, Moderna is set to produce 800,000 doses of the vaccine in Switzerland every day. Meanwhile, the UK has already approved the Pfizer, Moderna and Astra Zeneca vaccines. Israel has already vaccinated 1 million. 220 thousand citizens, and France vaccinated only 516 patients in the first week, that is, 20 times less than Lithuania. One can only guess that the French body does not tolerate American and German product while Sanofi’s “own” work is still on the way.
Does the European Medicines Agency follow this French logic, which is still reluctant to make decisions that can save lives? Already on the first day of December, Moderna submitted documents to the European Medicines Agency. If the EMA bureaucrats have different evidence than the FDA or UK regulator, it may be worth making it available to the general public. If there is no such evidence, then such a “stretch of the rubber” is at least incomprehensible to little ones. pandemic.
From my subjective point of view, the results of the 3 studies of the mentioned vaccines are unequivocal: side effects occur, but the vaccines work. In addition, the Chinese inactivated virus vaccine is also effective. Therefore, I can say one thing to the European bureaucracy: vaccinate the citizens of Europe ”, writes V. Kasiulevičius.
[ad_2]