COVID Vaccine Monitor study- Help us monitor the safety of COVID-19 vaccines in the UK

Why do this study?

The coronavirus (COVID-19) vaccines have been researched thoroughly before being given to the public. Only by being well researched may they be used. However, side effects after vaccination are always a possibility. The Drug Safety Research Unit would like to monitor this information. By doing so we will learn more about possible side effects as quickly as possible. Please find further information about the study in the Participant Information sheet.

Am I allowed to participate?

You may participate if you received your BOOSTER COVID-19 vaccine no longer than two days ago or you will be getting it soon.

If you would like to participate, please click here to start.

What do I need to keep in mind if I participate?

To be able to participate, you must register first. After registration you will receive a questionnaire with some general questions. Seven days after vaccination, you will receive the next questionnaire. In total you will receive six questionnaires over a period of approx. 3 months. Questionnaires need to be filled in via the study website. Each questionnaire takes 10-25 minutes to fill in. The questions are about the possible side effects that you may have experienced after vaccination. Even if you do not experience any side effects, we ask that you complete the questionnaires. Participation is completely voluntary. You can stop your participation at any time without explanation.

What will be done with my data?

Storage and security of your data will comply with General Data Protection Regulation (GDPR). For more information, please read the DSRU privacy statement.

Which side effects could I expect?

After any vaccination, a reaction can happen at the site of injection. It can be painful, red and/or swollen. You may feel generally unwell for a few days after the vaccination. Side effects such as headache, fever and muscle ache can also occur. For more information on COVID-19 vaccines and their side effects please visit: www.gov.uk/government/publications/covid-19-vaccination-what-to-expect-after-vaccination/what-to-expect-after-your-covid-19-vaccination

Most side effects occur within two days of vaccination, and they disappear within a few days. If you have any questions about possible side effects of COVID-19 vaccines, contact your GP.

Do you have questions about the study?

Please take a look at the FAQs. You may also contact Drug Safety Research Unit at covidmonitor@dsru.org

Any suspected side effects to COVID-19 vaccines can also be reported directly to the Medicines and Healthcare products Regulatory Agency (MHRA) on the Coronavirus Yellow Card reporting site below. This is a government system which is used to monitor the safe and effective use of COVID-19 vaccines and treatments available in the UK. https://coronavirus-yellowcard.mhra.gov.uk

Registration form

Mandatory questions in this registration form are marked with an asterisk (*).

The question below relates to the vaccinated. This can be yourself or the person for whom you want to enter the data:


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Question*

Are you filling in this form for yourself or on behalf of your child or on behalf of another person?


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required: true
type: Selection
key: Q2
Samepage: true
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Question*

Are you 16 years or older?


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required: true
type: MultipleChoice
key: SubCohort
Samepage: true
i
id: c22d5651-a4d1-47ab-ba3c-b1846eb3aa14

Question*

Do you fall into one of the special target groups?
Please note: Multiple answers can be selected.

** Examples of conditions that could affect the immune system: HIV/AIDS, transplants, autoimmune diseases (such as systemic lupus erythematosus, rheumatoid arthritis, psoriasis, psoriatic arthritis), leukaemia/lymphoma, or other disease that is affecting the immune system. Examples of immunosuppressant medications: medication for cancer or for chronic inflammatory conditions such as rheumatism, medication related to a compromised immune system, or medication to prevent rejection reactions after organ transplantation.


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required: true
type: Selection
key: Q4
Samepage: true
i
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Question*

With which booster vaccine have you been, or will you be vaccinated with?


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required: true
type: Selection
key: Q5
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Question*

Which situation applies to you?

Note: This is about the booster vaccination.


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required: true
type: Date
key: VacinationDate
Samepage: true
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Question*

On what date will you be receiving the COVID-19 booster vaccine? Please check your vaccination invitation if you have one.


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type: Date
key: VacinationDate
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Question*

On which date did you have your COVID-19 booster vaccine?


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PURPOSE OF THIS STUDY
The purpose of this study is to gather information on side effect (adverse reactions) caused by the COVID-19 booster vaccine. We will also compare reported suspected adverse reaction(s) between the different coronavirus vaccines. To expand the existing knowledge about the COVID-19 booster vaccines, it is important to gather information on possible adverse reactions in a structured way.

Who can participate?

  • Persons above 16 years old and soon receiving theCOVID-19 booster vaccine, or having received the COVID-19 booster vaccine no more than 2 days ago.

Informed consent
Questions which require an answer in this registration form are marked with an asterisk (*).

In order to participate with the COVID Vaccine Monitor study we need your consent. You will be asked to provide some general information. As soon as your informed consent has been submitted you will receive an email with a link to login get access to your questionnaires. To login you will receive a username and password seperately.

If you have any questions do not hesitate to contact the Drug Safety Research Unit by e-mail covidmonitor@dsru.org or telephone 02380 408600.
  • I have read the privacy statement and the information regarding this study. Any questions I had were answered by contacting the Drug Safety Research Unit.
  • I understand that participation is voluntary. I understand that I can decide at any time to stop my participation in this study and do not need to give a reason for my decision.
  • I understand that all information provided will be treated with strict confidentiality.
  • I give permission for my data to be used for the purpose of this study, namely, to gather information and expand the existing knowledge about the COVID-19 vaccines. It is important for the Drug Safety Research Unit to know precisely which vaccine brand was administered in order to compare the reported suspected adverse reaction between the administered coronavirus vaccines, gaining more insight in the relevant medical history of participants, reported adverse reactions, the nature of these reactions, the course of these reactions, possible risk factors and the consequences related to health.
  • I understand that my email address will only be used for registration and communication with the Drug Safety Research Unit
  • I understand that my data, except for personal data such as email address, postcode and date of birth, could be used for the wider European study. Several European countries will perform a similar study. Results of this study will be compared to each other. Any data shared for this purpose will be anonymous.
  • I am 16 years or older.


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Samepage: false
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Sometimes additional information about reported suspected adverse reactions is necessary. In this case we would like to be able to contact you. By doing so we are able to have complete and reliable data on the medical situation which essential for this study.

I give permission to be contacted for extra information about the reported suspected adverse reactions.


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key: Q10
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I give permission to be contacted by telephone for extra information about my pregnancy in case some information is lacking or some information is not entirely clear.


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Question*

Please enter your phone number


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type: Email
key: EmailAddress
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Question*

What is your Email address?
This is the email address where the emails will be received.


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Question*

What is your postal code?


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Question*

What is your first name?


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Question*

What is your year of birth?


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Question*

Are you 16 years or older?


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Question

Does your child fall into one of the special target groups?
Please note: Multiple answers can be selected.

** Examples of conditions that could affect the immune system: HIV/AIDS, transplants, autoimmune diseases (such as systemic lupus erythematosus, rheumatoid arthritis, psoriasis, psoriatic arthritis), leukaemia/lymphoma, or other disease that is affecting the immune system. Examples of immunosuppressant medications: medication for cancer or for chronic inflammatory conditions such as rheumatism, medication related to a compromised immune system, or medication to prevent rejection reactions after organ transplantation.


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required: true
type: Selection
key: Q18
Samepage: true
i
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Question*

Which booster vaccine has your child been, or will your child be, vaccinated with?


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Question*

Which situation applies to your child?

Note: This is about the booster vaccination.


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required: true
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key: VacinationDate
Samepage: true
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Question*

On what date will your child be receiving the COVID-19 booster vaccine? Please check the vaccination invitation if he/she has one.


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Question*

On which date did your child have his/her COVID-19 booster vaccine?


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PURPOSE OF THIS STUDY
The purpose of this study is to gather information on side effect (adverse reactions) caused by the COVID-19 booster vaccine. We will also compare reported suspected adverse reaction(s) between the different coronavirus vaccines. To expand the existing knowledge about the COVID-19 booster vaccines, it is important to gather information on possible adverse reactions in a structured way.

Who can participate?

  • A child under 18 years (who you will fill in the questionnaires for) who will soon receive the COVID-19 booster vaccine or who has received the COVID-19 booster vaccine no more than 2 days ago.

Informed consent
Questions which require an answer in this registration form are marked with an asterisk (*).
In order to participate with the COVID Vaccine Monitor study we need your consent. You will be asked to provide some general information. As soon as your informed consent has been submitted you will receive an email with a link to login get access to your questionnaires. To login you will receive a username and password seperately.

If you have any questions do not hesitate to contact the Drug Safety Research Unit by e-mail covidmonitor@dsru.org or telephone 02380 408600.
  • I have read the privacy statement and the information regarding this study. Any questions I had were answered by contacting the Drug Safety Research Unit.
  • I understand that participation is voluntary. I understand that I can decide at any time to stop the participation of my child in this study and do not need to give a reason for my decision.
  • I understand that all information provided will be treated with strict confidentiality.
  • I give permission for data of my child to be used for the purpose of this study, namely, to gather information and expand the existing knowledge about the COVID-19 vaccines. It is important for the Drug Safety Research Unit to know precisely which vaccine brand was administered in order to compare the reported suspected adverse reaction between the administered coronavirus vaccines, gaining more insight in the relevant medical history of participants, reported adverse reactions, the nature of these reactions, the course of these reactions, possible risk factors and the consequences related to health.
  • I understand that my email address will only be used for registration and communication with the Drug Safety Research Unit
  • I understand that my data, except for personal data such as email address, postcode and date of birth, could be used for the wider European study. Several European countries will perform a similar study. Results of this study will be compared to each other. Any data shared for this purpose will be anonymous.
  • I am 16 years or older.


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Sometimes additional information about reported suspected adverse reactions is necessary. In this case we would like to be able to contact you. By doing so we are able to have complete and reliable data on the medical situation which essential for this study.

I give permission to be contacted for extra information about the reported suspected adverse reactions.


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I give permission to be contacted by telephone for extra information about her pregnancy in case some information is lacking or some information is not entirely clear.


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Question*

Please enter your phone number


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Question*

What is your Email address?
This is the email address where the emails will be received.


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Question*

What is his/her postal code?


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Question*

What is his/her first name?


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Question*

What is his/her year of birth?


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Question*

Are you 16 years or older?


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Question*

Does the person you represent fall into one of the special target groups?
Please note: Multiple answers can be selected.

** Examples of conditions that could affect the immune system: HIV/AIDS, transplants, autoimmune diseases (such as systemic lupus erythematosus, rheumatoid arthritis, psoriasis, psoriatic arthritis), leukaemia/lymphoma, or other disease that is affecting the immune system. Examples of immunosuppressant medications: medication for cancer or for chronic inflammatory conditions such as rheumatism, medication related to a compromised immune system, or medication to prevent rejection reactions after organ transplantation.


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key: Q32
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Question*

Which booster vaccine has the person you represent been vaccinated with or will he/she be vaccinated with?


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Question*

Which situation applies to him/her?


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required: true
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key: VacinationDate
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Question*

On what date will he/she be receiving the COVID-19 booster vaccine? Please check the vaccination invitation if he/she has one.


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Question*

On which date did he/she have his/her COVID-19 booster vaccine?


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PURPOSE OF THIS STUDY
The purpose of this study is to gather information on side effect (adverse reactions) caused by the COVID-19 booster vaccine. We will also compare reported suspected adverse reaction(s) between the different coronavirus vaccines. To expand the existing knowledge about the COVID-19 booster vaccines, it is important to gather information on possible adverse reactions in a structured way.

Who can participate?

  • A person you represent who will soon receive the COVID-19 booster vaccine, or who has received the COVID-19 booster vaccine no more than 2 days ago.

Informed consentQuestions which require an answer in this registration form are marked with an asterisk (*).

In order to participate with the COVID Vaccine Monitor study we need your consent. You will be asked to provide some general information. As soon as your informed consent has been submitted you will receive an email with a link to login get access to your questionnaires. To login you will receive a username and password seperately.
If you have any questions do not hesitate to contact the Drug Safety Research Unit by e-mail covidmonitor@dsru.org or telephone 02380 408600.
  • I have read the privacy statement and the information regarding this study. Any questions I had were answered by contacting the Drug Safety Research Unit
  • I understand that participation of the person I represent is voluntary. I understand that I can decide at any time to stop the participation of the person I represent in this study and do not need to give a reason for my decision.
  • I understand that all information provided will be treated with strict confidentiality.
  • I give permission for data of the person I represent to be used for the purpose of this study, namely, to gather information and expand the existing knowledge about the COVID-19 vaccines. It is important for the Drug Safety Research Unit to know precisely which vaccine brand was administered in order to compare the reported suspected adverse reaction between the administered coronavirus vaccines, gaining more insight in the relevant medical history of participants, reported adverse reactions, the nature of these reactions, the course of these reactions, possible risk factors and the consequences related to health.
  • I understand that my email address will only be used for registration and communication with the Drug Safety Research Unit
  • I understand that my data, except for personal data such as email address, postcode and date of birth, could be used for the wider European study. Several European countries will perform a similar study. Results of this study will be compared to each other. Any data shared for this purpose will be anonymous.
  • As a legal representative, I am 16 years or older.


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Sometimes additional information about reported suspected adverse reactions is necessary. In this case we would like to be able to contact you. By doing so we are able to have complete and reliable data on the medical situation which essential for this study.

As a representative, I give permission to contact me for additional information about the reported suspected adverse reactions.


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I give permission to be contacted by telephone for extra information about his/her pregnancy in case some information is lacking or some information is not entirely clear.


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Question*

Please enter your phone number


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Question*

What is your email address?
This is the email address where the emails will be received about the questionnaires.


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Question*

12.c What is the postal code of the person you represent?


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Question*

What is the first name of the person you represent? *


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Question*

What is the year of birth of the person you represent? *

Result