Non-vaccinated travellers may face turbulance after pandemic: Lawyer
- Thread starter lenny2
- Start date
You're such a lost soul man! I guess the same bullshit you use to constantly claim they haven't isolated the virus now you spew bullshit and nonsense about the companies stating a claim of something that would trash their own product! YOU ARE LOST and foolish in everything you post!
Happy travels, oh wait, you won't be able to, sorry!
Repeating it over again does not make it fact.
Here are two charts of worldwide vaccines, the first chart contains vaccines that have completed their phase 3 trials and have been approved and what countries they have been approved by, the second chart is a list of vaccines still in trials or in their 3rd phase of trials.
If you notice in the first chart, which lists the vaccines that have completed their trials, it contains the Phizer, Moderna and Astra-Zenica brands.
https://www.raps.org/news-and-articles/news-articles/2020/3/covid-19-vaccine-tracker
Lame.
And off-base.
I compose and share my original thoughts. If I want to back up something I say or share something relevant to my original thoughts, then I will link to something else.
You just re-post Natural News and Steve Bannon bullshit and then parrot the propaganda they con gullible suckers with.
Why? Does he need a vaccine to fly around the world on YouTube?
Here is another.
Since I had my covid shot the nanites have enabled me to access 5G telepathically thereby enabling me to take down the Rogers network with a quick thought.
FUCK! I thought it was you! ConspiracyMan, get on this right away!!!!
PS..Thank God for my office landline.
ClinicalTrials.gov
clinicaltrials.gov
ClinicalTrials.gov
clinicaltrials.gov
What is an Emergency Use Authorization (EUA)?
An Emergency Use Authorization (EUA) is a mechanism to facilitate the availability and use of medical countermeasures, including vaccines, during public health emergencies, such as the current COVID-19 pandemic. Under an EUA, FDA may allow the use of unapproved medical products, or unapproved uses of approved medical products in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or conditions when certain statutory criteria have been met, including that there are no adequate, approved, and available alternatives. Taking into consideration input from the FDA, manufacturers decide whether and when to submit an EUA request to FDA.
Emergency Use Authorization for Vaccines Explained
FDA explains the Emergency Use Authorization for Vaccines
Reading and reading properly is your friend!! Always read the entire article before you post nonsense spin and bullshit!ClinicalTrials.gov
ClinicalTrials.gov
What is an Emergency Use Authorization (EUA)?
An Emergency Use Authorization (EUA) is a mechanism to facilitate the availability and use of medical countermeasures, including vaccines, during public health emergencies, such as the current COVID-19 pandemic. Under an EUA, FDA may allow the use of unapproved medical products, or unapproved uses of approved medical products in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or conditions when certain statutory criteria have been met, including that there are no adequate, approved, and available alternatives. Taking into consideration input from the FDA, manufacturers decide whether and when to submit an EUA request to FDA.
Emergency Use Authorization for Vaccines Explained
FDA explains the Emergency Use Authorization for Vaccineswww.fda.gov
Are the COVID-19 vaccines rigorously tested?
Yes. Clinical trials are evaluating investigational COVID-19 vaccines in tens of thousands of study participants to generate the scientific data and other information needed by FDA to determine safety and effectiveness. These clinical trials are being conducted according to the rigorous standards set forth by the FDA.
Initially, in phase 1, the vaccine is given to a small number of generally healthy people to assess its safety at increasing doses and to gain early information about how well the vaccine works to induce an immune response in people. In the absence of safety concerns from phase 1 studies, phase 2 studies include more people, where various dosages are tested on hundreds of people with typically varying health statuses and from different demographic groups, in randomized-controlled studies. These studies provide additional safety information on common short-term side effects and risks, examine the relationship between the dose administered and the immune response, and may provide initial information regarding the effectiveness of the vaccine. In phase 3, the vaccine is generally administered to thousands of people in randomized, controlled studies involving broad demographic groups (i.e., the population intended for use of the vaccine) and generates critical information on effectiveness and additional important safety data. This phase provides additional information about the immune response in people who receive the vaccine compared to those who receive a control, such as a placebo.
These are US based sites, last I checked we are in Canada and I posted the links to sites that concern Canada.ClinicalTrials.gov
ClinicalTrials.gov
What is an Emergency Use Authorization (EUA)?
An Emergency Use Authorization (EUA) is a mechanism to facilitate the availability and use of medical countermeasures, including vaccines, during public health emergencies, such as the current COVID-19 pandemic. Under an EUA, FDA may allow the use of unapproved medical products, or unapproved uses of approved medical products in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or conditions when certain statutory criteria have been met, including that there are no adequate, approved, and available alternatives. Taking into consideration input from the FDA, manufacturers decide whether and when to submit an EUA request to FDA.
Emergency Use Authorization for Vaccines Explained
FDA explains the Emergency Use Authorization for Vaccines
Health Canada and the FDA are two different entities in two different countries and do not follow the same guidelines, for example generic oxycontin is banned for use in the US but is approved for use in Canada.
But FYI Astra-Zenica actual primary completion date was March 5, 2021.
All vaccines are continually monitored once approved.
Interesting logic. The US actually makes the jab but won’t approve it until after 2023 (if trials are successful). Canada does not manufacturer any vaccines but is confident to approve it before US does. Canada would never ever approve a drug the US hasn’t? That would be madness. We have sooo much higher standards here for drug safety.
I think it depends on the country you are going to visit. For example, Iceland and Greece say travelers must show proof that they are vaccinated against Covid-19 or proof of a recent negative test. And it is better to be fully vaccinated before traveling to the United Arab Emirates. My friend has recently gone there. You know, he faced issues at the airport and even had to address the lawyers in UAE.
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