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COVID-19 vaccine safety report - 03-11-2022

Published

Four main COVID-19 vaccines are currently in use in Australia – Comirnaty (Pfizer), Spikevax (Moderna), Vaxzevria (AstraZeneca), and Nuvaxovid (Novavax). A Spikevax bivalent vaccine is also now available for use as a booster dose. To be registered for use, these vaccines must have met the TGA’s high standards for quality, safety and effectiveness.

The TGA closely monitors reports of suspected side effects (also known as adverse events) to the COVID-19 vaccines. This is the most intensive safety monitoring ever conducted of any vaccines in Australia.

We encourage people to report suspected side effects, even if there’s only a very small chance a vaccine was the cause. Learn more about causality and our COVID-19 vaccine safety monitoring and reporting activities.

Report a suspected side effect.

Summary

  • Vaccination against COVID-19 is the most effective way to reduce deaths and severe illness from infection. The protective benefits of vaccination far outweigh the potential risks.
  • The most up-to-date recommendations for use of the COVID-19 vaccines - external site are available from the Australian Technical Advisory Group on Immunisation (ATAGI).
  • Like all medicines, COVID-19 vaccines may cause some side effects. The most frequently reported include injection-site reactions (such as a sore arm) and more general symptoms, like headache, muscle pain, fever and chills. This reflects what was seen in the clinical trials.
  • We are carefully monitoring and reviewing reports of:
  • Myocarditis is a known but very rare side effect of Comirnaty (Pfizer) and Spikevax (Moderna). It is usually temporary, with most people getting better within a few days. Myocarditis is reported in around 1-2 in every 100,000 people who receive Comirnaty (Pfizer) and around 2 in every 100,000 of those who receive Spikevax (Moderna). It occurs in males and females but is more common after the second dose in boys aged 12-17 years (13 cases per 100,000 Comirnaty doses and 24 cases per 100,000 Spikevax doses) and men under 30 (9 cases per 100,000 Comirnaty doses and 23 cases per 100,000 Spikevax doses).
    • To 30 October 2022, the TGA has received 704 reports which have been assessed as likely to be myocarditis from about 44.2 million doses of Comirnaty (Pfizer) and 115 reports which have been assessed as likely to be myocarditis from about 5.4 million doses of Spikevax (Moderna).
  • Thrombosis with thrombocytopenia syndrome (or TTS) is a very rare but serious side effect of Vaxzevria (AstraZeneca). Our analysis shows it is reported in about 2 in every 100,000 vaccinated people following the first dose. The risk of TTS is much lower after the second dose (0.3 in every 100,000 vaccinated people).

Total adverse event reports following immunisation to 30 October 2022

  • 2.1

    Reporting rate per 1,000 doses

  • 1,867

    Total adverse event reports

  • 852,193 *

    Total doses administered

  • 647

    Total reports for Vaxzevria

  • 1,073

    Total reports for Comirnaty

  • 97

    Total reports for Spikevax

  • 12

    Total reports for Nuvaxovid

  • 9

    Total reports for brand not specified

* The Department of Health and Aged Care has recently updated COVID-19 vaccination reporting - external site to provide more accurate and timely information on the level of protection for the Australian population. Changes include the most up-to-date estimates of the resident Australian population and counting vaccine doses administered overseas and recorded in the Australian Immunisation Register (for brands recognised by the TGA). These changes are reflected in this report.

Reported side effects for COVID-19 vaccines

Anyone can report a suspected side effect, either:

  • directly to the TGA
  • through a health professional
  • by calling the NPS MedicineWise Adverse Medicine Events phone line for consumers.

You can report anonymously.

Learn more about how to report a suspected side effect to a COVID-19 vaccine.

The most frequently reported side effects suspected to be associated with the vaccines include headache, muscle and joint pain, fever, chills and nausea. Skin reactions at the site of the injection are also common and can include pain, swelling, redness and an itchy rash. These are recognised side effects of vaccination and are usually transient and mild. More information about what to expect and how to manage any symptoms after you receive your vaccine are available from NPS MedicineWise - external site.

Vaccine safety in children and adolescents

The most up-to-date vaccine recommendations for children are available from the Australian Technical Advisory Group on Immunisation (ATAGI).

The TGA is closely monitoring adverse event reports in people aged under 18 years. The rate of reports has stabilised with only a small number now being received each week.

To 30 October 2022, we have received about 4,290 reports from approximately 3.7 million doses of Comirnaty (Pfizer) and Spikevax (Moderna) in 12-17 year olds. The most commonly reported reactions are chest pain, headache, dizziness, nausea and fever.

The TGA is also closely monitoring adverse event reports in 5-11 year olds. To 30 October 2022, we have received about 1,650 reports from approximately 2.3 million Comirnaty (Pfizer) and Spikevax (Moderna) doses administered in this age group. The most common reactions reported included chest pain, vomiting, fever, headache and abdominal pain. We have received 39 reports of suspected myocarditis and/or pericarditis in this age group. Following review of the reports, 4 were likely to represent myocarditis and another 7 reports were likely to represent pericarditis.

Survey data from AusVaxSafety show that:

  • children and adults are more likely to experience side effects after a second COVID-19 vaccine dose, but most reactions are mild and temporary.
  • children aged 5-11 years report fewer side effects than older Australians following a second dose.

These observations are consistent with what was reported in the clinical trials and from overseas experiences.

More information and frequently asked questions about COVID-19 vaccines in children are available on the National Centre for Immunisation Research and Surveillance - external site website.

Safety monitoring in the under 5s

ATAGI recommends vaccination for children aged 6 months to less than 5 years - external site who are at increased risk of severe COVID-19. This includes children with severe immunocompromise, complex or multiple health conditions, or disability with significant or complex health needs.

The TGA will be closely monitoring reports of adverse events in younger children. AusVaxSafety - external site has also started monitoring vaccine safety through a short online survey to parents or carers after their child has been vaccinated.

The paediatric Spikevax (Moderna) vaccine has been tested in around 5,500 children aged 6 months to under 5 years in the KidCOVE clinical trial. This study found the safety and efficacy of the vaccine was similar to that seen in adults. Most adverse effects were mild–moderate, lasted 1–2 days, and were generally reported after the second dose. Common reactions included irritability and crying, redness and swelling at the injection site, tiredness, fever, muscle pain and swelling or tenderness of lymph nodes near the injection site. Fever was more common in this age group compared to older children and adults, and children who had previously had SARS-CoV-2 infection were more likely to have side effects after vaccination.

In the US, where over a million doses of the paediatric mRNA vaccines have already been given, analysis of vaccine surveillance data - external site by the Centers for Disease Control and Prevention reveals that most adverse events are mild-moderate. Serious events were very rare and no unexpected safety concerns were detected. This is consistent with findings from the clinical trials.

Booster doses

The most up-to-date vaccine recommendations for booster doses - external site are available from ATAGI.

The TGA is monitoring the safety of booster vaccine doses in adults. A booster dose is an additional vaccine dose given after the primary vaccine course. In people who have recently had COVID-19, a 3-month interval is recommended before having their next scheduled dose.

In this report, we refer to a booster dose as either a third or fourth dose. To 30 October 2022, approximately 14.3 million people have received boosters in Australia. This includes 5 million people who have received a fourth dose. We have received approximately 9,750 reports of suspected adverse events identified as occurring after a booster dose.

Adverse event reports for booster doses include a small number of myocarditis and pericarditis cases. This is a recognised risk with the Comirnaty (Pfizer) and Spikevax (Moderna) vaccines and we are closely monitoring these events. So far, reports of myocarditis after a booster dose are very rare, occurring in less than 1 in every 100,000 vaccinated people.

The most common adverse events reported to the TGA following a booster dose are headache, swollen lymph nodes (also called lymphadenopathy), chest pain, muscle pain and fever. Swollen lymph nodes are a normal and known side effect of vaccines. They occur when the immune system is stimulated and were seen in the COVID-19 vaccine clinical trials. More detail about this potential side effect is given in a previous vaccine safety report on the 6 January 2022.

Reports of death in people who have been vaccinated

Vaccines can lead to death in extremely rare instances. However, most deaths that occur after vaccination are not caused by the vaccine. In large populations in which a new vaccine is given, there are people with underlying diseases who may die from these diseases. When a vaccine is given in that same population, the link between the vaccine and death is usually coincidental – not caused by the vaccine. These deaths are carefully reviewed for whether vaccines could be the cause and for the vast majority that is not the case.

The TGA closely reviews all deaths reported in the days and weeks after COVID-19 vaccination. Read more about this process in a previous report. Since the beginning of the vaccine rollout to 30 October 2022, about 63.9 million doses of COVID-19 vaccines have been given in Australia. The TGA has identified 14 reports where the cause of death was linked to vaccination from 943 reports received and reviewed. As previously reported, 13 of these deaths occurred after the first dose of Vaxzevria (AstraZeneca) – 8 were associated with thrombosis with thrombocytopenia syndrome (TTS) cases, 2 were linked to Guillain-Barre syndrome (GBS), 2 related to very rare conditions involving the nervous system, and one was a case of immune thrombocytopenia (ITP). One of the deaths occurred after a booster dose of the Spikevax vaccine and was related to myocarditis. Details have been published in a previous report.

The 14 deaths likely to be related to vaccination occurred in people aged 21–81 years old. There have been no deaths in children or adolescents determined to be linked to COVID-19 vaccination.

AusVaxSafety - a national survey on COVID-19 vaccine safety

AusVaxSafety has collected responses from over 6 million Australians about adverse events after they have received a COVID-19 vaccine. A recent analysis of survey data - external site affirms the safety of the Comirnaty (Pfizer) and Vaxzevria (AstraZeneca) vaccines. Results largely reflect what was seen in the clinical trials, with injection-site pain, fatigue, headache, and muscle pain being the most common reactions. Most reactions were short-lived and just under 1% of respondents sort medical advice because of an adverse reaction in the first 3 days after vaccination.

On the AusVaxSafety website - external site, survey results are presented for each COVID-19 vaccine:

For each vaccine, survey results are given for different age groups and different populations, such as Aboriginal and Torres Strait Islander people, those affected by cancer or who have received a transplant, and pregnant women.

Comirnaty (Pfizer) mRNA vaccine

The Comirnaty (Pfizer) vaccine is provisionally approved for adults and children aged 5 years and over. To 30 October 2022, about 44.2 million doses have been administered in Australia.

The TGA is actively investigating reports of myocarditis (inflammation of the heart) and/or pericarditis (inflammation of the membrane around the heart) associated with mRNA vaccines. We continue to work with international regulators on this safety signal (see below).

A new bivalent vaccine from Pfizer was provisionally approved as a booster dose in adults on 27 October 2022. In an ongoing clinical trial, it was found to trigger a better immune response to the BA.1 Omicron variant compared to the original Pfizer vaccine, and a similar response to the ancestral COVID-19 strain. Recommendations for the use of this new vaccine in Australia are being considered by ATAGI.

Up-to-date information for Comirnaty (Pfizer), including details of potential side effects , can be found in the Consumer Medicine Information - external site (for consumers) and Product Information - external site (for health professionals).

Spikevax (Moderna) mRNA vaccines

The original Spikevax vaccine is provisionally approved for adults and children aged 6 years and over. To 30 October 2022, about 5.4 million doses have been administered in Australia. A paediatric formulation is available for children aged from 6 months to 5 years (or less than 6 years).

A new Spikevax bivalent vaccine has recently been provisionally approved for use as a booster dose in adults. This vaccine is designed to trigger an immune response to the original COVID-19 virus and to the BA.1 Omicron variant. It should be given at least 3 months after the previous vaccine dose according to the latest ATAGI guidelines - external site. FAQs about the bivalent vaccine are answered on the National Centre for Immunisation Research and Surveillance website - external site.

The TGA is actively investigating reports of myocarditis (inflammation of the heart muscle) and/or pericarditis (inflammation of the membrane around the heart) associated with mRNA vaccines. We continue to work with international regulators on this safety signal (see below).

Up-to-date information for Spikevax (Moderna), including details of potential side effects, can be found in the Consumer Medicine Information - external site (for consumers) and Product Information - external site (for health professionals).

Nuvaxovid (Novavax) vaccine

The Nuvaxovid (Novavax) vaccine is provisionally approved for adults. To 30 October 2022, about 226,400 doses of Nuvaxovid (Novavax) have been administered in Australia.

The TGA has received a small number of reports of suspected myocarditis and/or pericarditis in people who have received the Nuvaxovid (Novavax) vaccine. After assessing these against a set of internationally accepted criteria, 9 cases were likely to represent myocarditis and 30 were likely to represent pericarditis.

Anaphylaxis, paraesthesia and hypoaesthesia (tingling and numbness of the skin) have also been added to the Nuvaxovid (Novavax) PI as potential adverse events. These adverse events are also recognised for other COVID-19 vaccines in use in Australia.

More information for Nuvaxovid (Novavax), including details about its ingredients and potential side effects, can be found in the Consumer Medicine Information - external site (for consumers) and Product Information - external site (for health professionals).

Vaxzevria (AstraZeneca) vaccine

The Vaxzevria (AstraZeneca) vaccine is provisionally approved for adults. To 30 October 2022, about 13.8 million doses of Vaxzevria (AstraZeneca) have been administered in Australia. However, since the end of 2021 very few doses are being used.

The TGA is closely monitoring rare reports of blood clots with low blood platelets (also called thrombosis with thrombocytopenia syndrome or TTS) linked to this vaccine, immune thrombocytopenia (ITP) and Guillain-Barre Syndrome (GBS). These are rare but serious side effects, with TTS reported in about 2 in every 100,000 people after receiving Vaxzevria (AstraZeneca) and ITP and GBS reported in about one in every 100,000 people. Detailed information of our analysis of these adverse effects is available in a previous vaccine safety report.

With only limited use of the Vaxzevria (AstraZeneca) vaccine now in Australia, we have not received any new reports of confirmed or probable TTS this year. The total number of TTS cases reported in Australia is 173. Of these, 149 (83 confirmed, 66 probable) were related to a first dose of Vaxzevria (AstraZeneca) and 24 (5 confirmed, 19 probable) to a second dose. There has been no change in the reporting rates for ITP, GBS or TTS this year but we continue to monitor for reports to identify new information about these risks.

More general information for Vaxzevria (AstraZeneca), including details of potential side effects can be found in the Consumer Medicine Information - external site (for consumers) and Product Information - external site (for health professionals).

Myocarditis and pericarditis with mRNA vaccines

ATAGI continues to emphasise that the protective benefits of the mRNA vaccines far outweigh the rare risk of these side effects - external site.

ATAGI has advised that people who have had suspected vaccine-related myocarditis or pericarditis should defer further doses of an mRNA COVID-19 vaccine until at least 6 weeks after their symptoms have resolved. They should also discuss future vaccine doses with their treating doctor. Refer to expert Guidance on myocarditis and pericarditis after mRNA COVID-19 vaccines - external site for more detail about revaccination.

What are myocarditis and pericarditis?

Myocarditis is inflammation of the heart, and pericarditis is inflammation of the membrane around the heart. These conditions can occur separately or together (myopericarditis) as rare adverse events after vaccination with the mRNA vaccines Comirnaty (Pfizer) and Spikevax (Moderna).

Myocarditis and pericarditis are seen in the general population from a variety of causes, including after COVID-19 disease. Not all cases that occur after vaccination are necessarily caused by the vaccine.

When do myocarditis and pericarditis occur?

Cases typically occur within 10 days, with symptom onset often within 5 days of vaccination. Some published evidence - external site found pericarditis symptoms may occur later, commonly 2-3 weeks after vaccination. Our analysis indicates that most of the patients with likely myocarditis experienced symptoms within 3 days of vaccination.

Who is at risk of these heart problems?

Myocarditis can occur in males and females but is more commonly reported after the second dose in boys aged 12-17 years (13 cases per 100,000 Comirnaty doses and 24 cases per 100,000 Spikevax doses) and men under 30 (9 cases per 100,000 Comirnaty doses and 23 cases per 100,000 Spikevax doses). However, even in this population it remains rare.

Pericarditis is reported in about 2 in every 100,000 people who receive an mRNA vaccine. It is reported more often after the Nuvaxovid (Novavax) vaccine, with about 13 reports for every 100,000 doses administered, most commonly in males aged 18-49 years old. The pericarditis rate for Nuvaxovid is less certain than for Comirnaty and Spikevax due to the low numbers of Nuvaxovid vaccine doses given.

Do myocarditis and pericarditis occur after a booster dose?

Myocarditis and pericarditis can occur after a booster dose. It is rare but can sometimes be serious. Australian and international data indicate that myocarditis and pericarditis are reported less commonly after a booster dose than after a second dose. The rate of reporting of myocarditis and pericarditis is less than 1 in every 100,000 people after a booster dose.

To 30 October 2022, from approximately 14.3 million people who have received booster doses, we have received 63 reports of likely myocarditis and 112 reports of likely pericarditis for Comirnaty (Pfizer) and 28 reports of likely myocarditis and 31 reports of likely pericarditis for Spikevax (Moderna). The median age of affected individuals was 34 years old.

How serious are myocarditis and pericarditis?

Myocarditis is often mild, and cases usually resolve after a few days with treatment and rest. Serious cases of myocarditis can occur and have been reported in Australia and overseas. A fatal case linked to a booster dose of the Spikevax vaccine has been reported previously.

Our latest analysis of data from adverse event reports has found 56% of the patients with likely myocarditis and 19% with likely pericarditis were admitted to hospital. Twenty-three people with myocarditis and 9 people with pericarditis were treated in intensive care. This represents less than 1% of all likely cases.

What myocarditis and pericarditis symptoms should I look out for?

We encourage people to seek medical attention if they experience symptoms that could suggest myocarditis or pericarditis. This includes chest pain, palpitations (irregular heartbeat), fainting or shortness of breath, particularly if they occur within 1–5 days of vaccination.

What does the TGA know about myocarditis and pericarditis in Australia?

Reports received by the TGA of suspected myocarditis and pericarditis for the mRNA vaccines are provided in Table 1. We have reviewed these reports against an internationally accepted criteria to classify the likelihood of myocarditis.

Reporting rates of likely myocarditis and pericarditis appear similar to overseas rates and are given in Tables 2 and 3.

Reports of suspected myocarditis and pericarditis

Table 1. Reports of suspected myocarditis and pericarditis received by the TGA to 30 October 2022¥
 

Comirnaty (Pfizer)

(44.2 million doses given)

Spikevax (Moderna)

(5.4 million doses given)

 All casesCases in adolescents (12-17 years)All casesCases in adolescents (12-17 years)
Suspected myocarditis cases*1,41622820134
Likely myocarditis†‡Level 1681181
Level 24841448723
Level 315211203
Unlikely myocarditis39033433
Insufficient information32229434
Suspected pericarditis cases2,84218130613
Likely pericarditis£1,082771162

Notes for Table 1

* Cases reporting both myocarditis and pericarditis are included in suspected myocarditis cases.

¥ The total number of reports can fluctuate slightly over time as duplicate reports may be identified and deleted and cases may be reclassified after receiving more information.

‡ Cases classified as level 1 are confirmed to be myocarditis based on strong clinical evidence including the patient’s symptoms, and results of tests and imaging indicating a diagnosis of myocarditis. Level 2 cases are probably myocarditis based on a combination of symptoms and routine tests for heart conditions. Level 3 cases are possibly myocarditis based on symptoms and a doctor’s report that myocarditis is the most likely diagnosis in the absence of medical tests and investigations. For all cases of suspected myocarditis, where possible, other known causes of the patient’s symptoms or test results are ruled out before cases are classified.

† The youngest case classified as 'likely myocarditis' to date is 6 years old.

£ Classification of likely pericarditis is based on the patient’s symptoms and test results and the absence of other known causes of pericarditis.

Rates of likely myocarditis

Table 2. Rates of likely myocarditis cases following Comirnaty (Pfizer)‡
Age (years)All dosesSecond doses
 Rate* per 100,000 dosesRate* per 100,000 doses
MaleFemaleMaleFemale
5-110.30.10.20
12-178.11.713.12.8
18-295.11.59.22.7
30-392.40.93.21.0
40-490.90.91.41.7
50-590.70.30.70.4
60-690.40.30.40.4
70+0.10.200.4
All ages*2.40.94.71.5
Table 3. Rates of likely myocarditis cases following Spikevax (Moderna) †
Age (years)All dosesSecond doses
 Rate* per 100,000 dosesRate* per 100,000 doses
MaleFemaleMaleFemale
12-1712.12.923.65.0
18-2910.42.023.24.7
30-393.10.75.00
40-491.70.83.32.0
50-590.91.52.02.5
60-6900.200
70+00.100
All ages*3.31.111.92.7

Notes for Table 2 and Table 3

* The rate includes cases of myocarditis that occurred after vaccination but may not be vaccine related.

‡ To 30 October 2022, from about 2.3 million vaccine doses given, 4 likely cases of myocarditis have been reported in children aged 5-11 years following vaccination with Comirnaty (Pfizer).

† The rates for Spikevax (Moderna) are less certain due to low numbers of cases overall and small changes in case number can lead to fluctuations in the rates for different groups.

Rates of likely pericarditis

Table 4. Rates of likely pericarditis cases following the mRNA vaccines
Age (years)Rate* per 100,000 doses
 Comirnaty (Pfizer)Spikevax (Moderna)
5-11‡0.3-
12-172.30.6
18-293.94.9
30-394.14.6
40-492.52.5
50-591.51.0
60-690.70.3
70+0.20.1
All ages*2.52.2

Notes for Table 4

* The rate includes cases of pericarditis that occurred after vaccination but may not be vaccine related.

‡ To 30 October 2022, from about 2.3 million Comirnaty (Pfizer) vaccine doses given, 1 probable and 6 possible cases of pericarditis have been reported in children aged 5-11 years. No cases of pericarditis have been reported following Spikevax (Moderna) in this age group.

For more information, see guidance on myocarditis and pericarditis - external site developed by ATAGI and the Cardiac Society of Australia and New Zealand (CSANZ).

Watch this video to find out how the TGA monitors and reports the safety of COVID-19 vaccines - external site

COVID-19 vaccines: Frequently asked questions – 12 October 2022 - external site

COVID vaccines – is it true? – 25 August 2022 - external site

Up-to-date recommendations for the use of COVID-19 vaccines in Australia – 24 October 2022 - external site

AusVaxSafety: Pfizer COVID-19 vaccine safety data – Child participants - external site

Latest advice on COVID-19 vaccination for pregnant and breastfeeding women - external site

TGA COVID-19 vaccines hub

Australian Government Department of Health COVID-19 vaccines hub - external site

COVID vaccine information in your language - external site

Database of Adverse Event Notifications (DAEN)

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