![]() The first adverse event reports for the Comirnaty vaccine are now available in the TGA’s public Database of Adverse Event Notifications (DAEN). Public access to vaccine adverse event reports The most common reactions reported for the Comirnaty (Pfizer) COVID-19 vaccine in the week of 17- were headache, muscle pain, lethargy, fever and injection site reactions. The most common reactions reported for the AstraZeneca COVID-19 vaccine in the week of 17- were headache, muscle pain, fever, chills and fatigue. They include headache, muscle and joint pain, fever and injection site reactions. The AEFI most commonly reported to the TGA following COVID-19 vaccines are side effects that are observed with vaccines generally. In the week of 17- we received 1609 AEFI reports for COVID-19 vaccines. Learn more about how the TGA identifies and responds to safety issues. Gathering reports of adverse events following immunisation (AEFI) is just the first step in determining whether or not the effect is related to the vaccine and whether a significant safety issue is involved. Reported side effects for COVID-19 vaccines ![]() When assessed using the United Kingdom (UK) case definition, six cases are confirmed TTS and three are probable. Nine additional cases of blood clots with low blood platelets have been assessed as thrombosis with thrombocytopenia syndrome (TTS) likely to be linked to the AstraZeneca vaccine. The most frequently reported suspected side effects associated with Comirnaty (Pfizer) and AstraZeneca COVID-19 vaccines continue to be events that were seen in the clinical trials, and are commonly experienced with vaccines generally. Learn about the TGA’s COVID-19 vaccine safety monitoring and reporting activities or report a suspected side effect. Most of the adverse events reported to the TGA are expected side effects seen with vaccines generally. The Therapeutic Goods Administration (TGA) closely monitors suspected side effects (also known as adverse events) from the use of COVID-19 vaccines.
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