Essential workers will be among the first in the nation to be eligible to take the new COVID-19 vaccines, which evidence shows will provide significant protection against the deadly disease. Three vaccines are currently available. The vaccines from Pfizer and from Moderna both use messenger RNA (mRNA) technology.This technology does not use any live virus particles. You will not be exposed to the virus that causes COVID-19.
A third vaccine, by Johnson & Johnson (J & J), is a viral vector vaccine. It is made from an inactivated adenovirus, the virus that causes the common cold, and contains a piece of DNA that instructs the body to make the COVID-19 spike protein. The use of genetic instructions makes the Johnson & Johnson vaccine similar to, but not exactly the same as the Pfizer and Moderna vaccines.
All three vaccines have a very high level of effectiveness. Pfizer has a 95 percent rate and Moderna has a 94 percent rate. To be effective, both of these vaccines require two shots, given a few weeks apart. Vaccines cannot be mixed and matched between doses. The length of vaccine-induced immunity is not known at this time, and booster shots may be required.
The J & J vaccine was 85% effective in preventing severe/critical illness and 66% effective in preventing symptomatic illness 28 days after vaccination. Importantly, it was 100% effective in preventing hospitalization and death from COVID-19. The J & J vaccine only requires one shot to be effective.
The length of vaccine-induced immunity is not known at this time, and booster shots may be required.
Some people who get a COVID-19 vaccine will experience side effects, particularly after a second dose. The side effects of the vaccine appear to be minor and temporary, including injection site pain, fatigue, and occasional fever, headache, or aching muscles and joints. These side effects fade within 1-2 days; no long-term effects have been detected thus far.
While the vaccine provides significant protection, it is not 100% effective. There is a slight chance that vaccinated individuals can still get infected with a mild case of the virus. Those who have taken the vaccine may be able to spread the virus to others at home and at work. Thus it is critical that everyone continue to wear PPE and follow public health protocols for the foreseeable future.
The Pfizer and Moderna vaccines both use messenger RNA (mRNA) technology. They do not use any live virus particles, meaning individuals will not be exposed to the virus that causes COVID-19. Instead, the messenger RNA -- a piece of genetic code -- directs cells to make the COVID-19 spike protein themselves, after which point the immune system creates the antibodies that fight COVID-19, providing a significant level of immunity.
Johnson & Johnson (J & J), is a viral vector vaccine. It is made from an inactivated adenovirus, the virus that causes the common cold, and contains a piece of DNA that instructs the body to make the COVID-19 spike protein. J & J used a modified adenovirus that can enter cells but can’t replicate inside them or cause illness. This in turn triggers an immune system response, giving you protection should you ever be exposed to the real virus in the future. The use of genetic instructions makes the Johnson & Johnson vaccine similar to, but not exactly the same as the Pfizer and Moderna vaccines.
Both Pfizer and Moderna utilized mRNA, which is easy to make in the laboratory, saving years in development and accelerating the creation of the vaccine. In clinical trials for both vaccines, over 73,000 people from the U.S. and around the world received injections, including over 25,000 people from the communities most impacted by COVID-19, including Black, Latinx, and older people.
The Johnson & Johnson vaccine utilizes older technology used most recently to develop an ebola vaccine. This approach uses different viruses engineered to be harmless, but still capable of inducing your cells to make the proteins needed to create an immune response. It was tested on 44,325 people in Brazil, South Africa, Chile, the US, Argentina, Colombia, Peru and Mexico, including Black, Latinx, AAPI and older people.
Vaccines must be approved by the Food and Drug Administration (FDA) before distribution. The FDA bases its decision to approve or not approve a vaccine on data from clinical trials. Independent experts and career scientists determine the vaccine’s safety based on the extent of side effects. If the clinical trial data shows enough evidence of efficacy and safety, the FDA will approve the vaccine.
 Thanks to SEIU 1199UHE for developing this fact sheet, in close consultation with doctors and other medical professionals.