Adverse events following COVID-19 infection and/or COVID-19 vaccination
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients who have provided written informed consent form by signing a consent form to participate in this research. In case of deceased subjects, informed consent will be obtained from a legally authorized representative. 2.Patients who have developed adverse events after COVID-19 infection and/or COVID-19 vaccination, or after blood transfusion from a donor who has received a COVID-19 vaccine. 3.Patients who have specimens collected and stored during routine clinical practice or specimens preserved by autopsy; patients who are able to provide blood samples or biopsy specimens collected in addition to routine clinical practice, or surgical specimens obtained during routine clinical practice; or patients who are able to newly provide urine or sweat samples. 4.No upper or lower age limit is set.
Exclusion criteria
Exclusion criteria: None.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Not applicable because the primary outcome is immunopathological and molecular biological analyses on an individual case basis. | — |
Countries
Japan
Contacts
Japanese Society for Vaccine-related Complications NA