"Normally vaccines take years to develop. In the case of Covid-19, we developed them in a few months. They can't have been properly tested for safety in such a short time."
"Four people got Bell's Palsy after taking the Pfizer vaccine. This was caused by the vaccine."
"Reports from Norway in January 2021 indicate that 23 elderly people died shortly after having the Pfizer vaccine. This vaccine is not safe."
"What about long-term side effects? We simply haven't had enough time to test for these."
1) The speed of the trials hasn't compromised how much data has been collected on safety. It usually takes years or occasionally decades to approve a vaccine. There are several reasons why vaccines have been tested and approved so quickly for Covid-19, and they have not resulted in a compromise of safety.
Firstly, different phases of the trials have been run in parallel instead of sequentially, which would take far longer. This has been possible in part due to greater funding and collaboration. Secondly, the disease has been pervasive enough that participants have been recruited very rapidly, and a large number of people in the trials have caught the virus quickly, meaning scientists have been able to quickly find out whether vaccines would protect recipients in their trials, compared to those who received a placebo. Thirdly, for some vaccines, regulators have been investigating the data on vaccines while trials were ongoing instead of after they had completed, which has also saved time. In sum, vaccines have had to go through the same phases of trials, had the same data collected and had to pass the same standards as in usual times.
"The safety and efficacy of the [Pfizer] vaccine have been assessed in clinical trials of over 44,000 people in six countries: USA, Germany, Brazil, Argentina, South Africa and Turkey. The trial reported that the vaccine can prevent 95% of COVID-19 cases. This means that in a group of 20 people who are vaccinated, if all are exposed to the coronavirus, 19 people will be prevented from getting COVID-19. The trial also showed that the vaccine provides similar protection in people of all ages, races and ethnicities.
"The [AstraZeneca] vaccine has been tested by the University of Oxford in clinical trials of over 23,000 people in the UK, Brazil and South Africa. AstraZeneca are also running a further trial with 40,000 people in the USA, Argentina, Chile, Columbia and Peru.
"Interim results from the UK and Brazil trials showed that the vaccine can prevent 70.4% of COVID-19 cases. This was calculated across two different groups of people, who received two different dose regimens."
The clinical trials run to test these vaccines were thus extremely large - with so many participants, there are many opportunities to monitor for side effects.
Even before the final trials, the vaccines had been through an extensive testing process. The Oxford Vaccine Knowledge Project describes the many different stages of testing the vaccines have to go through before and after use. They are tested on individual cells, then non-human animals (usually mice), then increasingly large numbers of human participants. Even after the large clinical trials, the vaccines are monitored for safety and rare side effects. Any severe side effects were referred to the patient's doctor, as well as an independent safety committee.
As would be expected for any vaccine, minor side effects were common in both the Pfizer and AstraZeneca vaccines. These included arm pain around the injection site, fatigue, headache, and fever. These rarely lasted more than a few days.
The same goes for any other medical condition that appears after a vaccine. Ask yourself: how likely was it that the person would have developed the condition anyway? Events with a probability of many thousands to one will occur quite a few times in studies of tens of thousands of participants.