In a press release on Tuesday, the FDA has declared the monovalent Pfizer and Modena mRNA Covid-19 vaccines are no "Longer authorized for use in the United States." The decision was made through a recent amendment to the Emergency Use Authorizations of the Moderna and Pfizer Covid-19 bivalent vaccines.
In the amendment, the FDA ruled the bivalent Moderna and Pfizer Covid-19 vaccines will be used for all doses and monovalent doses will no longer be authorized.
The FDA claims the decision was made in order to simplify the vaccine process, but many people who have already received the monovalent Covid-19 vaccine are questioning why the FDA is making the decision now.
Read: Dr. Peter McCullough On "The Holy Grail Of COVID-19 Vaccine Detoxification" Per The FDA: Today, the U.S. Food and Drug Administration amended the emergency use authorizations of the Moderna and Pfizer-BioNTech COVID-19 bivalent mRNA vaccines to simplify the vaccination schedule for most individuals.
The monovalent Moderna and Pfizer-BioNTech COVID-19 vaccines are no longer authorized for use in the United States.
Most individuals, depending on age, previously vaccinated with a monovalent COVID-19 vaccine who have not yet received a dose of a bivalent vaccine may receive a single dose of a bivalent vaccine.
Most individuals who have already received a single dose of the bivalent vaccine are not currently eligible for another dose.
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