Post-COVID-19 vaccination syndromes
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Patients providing written consent for registry inclusion will be incorporated into the study. - Patients who visited or were admitted to a research institution between December 2020 and August 31, 2023, and exhibited symptoms deemed by researchers as definitively or likely related to the vaccine.
Exclusion criteria
Exclusion criteria: No exclusion criteria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint of the study is the characterization of adverse events that are definitely or almost certainly related to the novel coronavirus vaccine. | — |
Secondary
| Measure | Time frame |
|---|---|
| - Occurrence or non-occurrence of Grade3 or above adverse events - Presence or absence of adverse events(adverse reactions) for which acausal relationship could not be ruled out - Time to onset of adverse events, Grade3 or above adverse events and adverse reactions | — |
Countries
Japan
Contacts
Japanese Society for Vaccine-related Complications Not applicable