- Description: An overview of Covid-19 Vaccine Side Effects, Allergic Reactions and Deaths worldwide.
- An open source developer-created searchable data and information site to learn more about Adverse Health events related to the COVID vaccines. Events include reactions and deaths following vaccination.
Adverse Events Following
Immunization (AEFI) Data
Dates: From mid-December 2020 – February 12th, 2021
- COVD Vaccine Doses Administered in Canada: 1,221,539
- 957 AEFI’s (.08% of all doses administered)
- 140 Serious AEFI’s (.01% of all doses administered)
- 817 Non-serious AEFI’s (.07% of all doses administered)
- # of reported adverse
events was highest among females and those aged 18 to 49.
Definition of Serious AEFI:
An event is considered serious if it:
- results in death
- is life-threatening (an
event/reaction in which the patient was at real, rather than hypothetical,
risk of death at the time of the event/reaction)
- requires in-patient
hospitalization or prolongation of existing hospitalization
- results in persistent or
significant disability/incapacity, or
- results in a congenital
anomaly/birth defect
Anaphylaxis: Among the 140 serious reports, the most frequently reported adverse event was anaphylaxis.
- Blood (1437)
- Cardiac (712; 17 deaths)
- Congenital (1)
- Ear (445)
- Endocrine (3)
- Eye (823)
- Gastro-intestinal (6605; 8 deaths)
- General (19354; 77 deaths)
- Hepatic (Liver) (10)
- Immune System (includes Allergic and Anaphylaxis reactions) (308)
- Infections (includes COVID-19; pg. 19) (1186; 22 deaths)
- Injuries (224)
- Investigations into various health events (653)
- Metabolic (357; 1 death)
- Misc.: Product contamination; device malfunction (8)
- Muscle & tissue (8129)
- Neoplasms (6)
- Nervous System (11,160; 11 deaths)
- Pregnancy (includes miscarriages, 5) (8)
- Psychiatric (830)
- Renal & Urinary (120)
- Reproductive & Breast (187)
- Respiratory (2397; 6 deaths)
- Skin (3947; 1 death)
- Social circumstances (disability) (11)
- Surgical & medical procedures (17)
- Vascular (676)
- Browse AE data post-COVID vaccine administration. Videos also available.
- VAERS accepts reports of adverse events and reactions that occur following vaccination. Healthcare providers, vaccine manufacturers, and the public can submit reports to the system.
- VAERS is designed to rapidly detect unusual or unexpected patterns of adverse events, also known as “safety signals.”
Vaccine Adverse Events Reporting System (VAERS) (official site)
Retrieved from: https://vaers.hhs.gov/data.html.
Copyright © 2021.Tracey Young/Canadian Advocacy Centre for Health, Safety and Justice. All Rights Reserved.
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