Taking Back Our Rights, Freedoms and Liberties (TBORFAL)
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Vaccine Adverse Event Reporting
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1. Are you reporting this adverse event for yourself?
Yes
No
2. Are you reporting this adverse event for someone else?
Yes
No
3. If you are reporting for someone else, what is your position relative to the patient?
Physician
health care worker
pharmacist
Parent
Family Member
lawyer
consumer
Other
3a. If Selected Others Please Specify
4. Is the patient male or female?
Male
Female
5. What was patient’s age at the time of the vaccination?
0 to 5 years
5 to 10 years
11 to 16 years
17 years to 20 years
21 to 30 years
40 to 70 years
Over 70 years
6. What was patient’s age at the time of the time of the reaction?
0 to 5 years
5 to 10 years
11 to 16 years
17 years to 20 years
21 to 30 years
40 to 70 years
Over 70 years
7. What is patient’s weight?
Below 40 pounds
41 to 80 pounds
81 to 120 pounds
Over 120 pounds
8. Which vaccine was taken?
Astra Zeneca
Pfizer – BioNTech
Moderna
Johnson and Johnson
Other, please specify
If Selected Others Please Specify
9. In which continent was the vaccine administered?
North America
Africa
Europe
Oceania
South America
Asia
9a. Please Specify the country where the vaccine was administered?
9b. If vaccine was administered in USA which state was it administered in?
North America
USA
Alabama
Alaska
Arizona
Arkansas
California
Colorado
Connecticut
Delaware
District of Columbia
Florida
Georgia
Hawaii
Idaho
Illinois
Indiana
Iowa
Kansas
Kentucky
Louisiana
Maine
Maryland
Massachusetts
Michigan
Minnesota
Mississippi
Missouri
Montana
Nebraska
Nevada
New Hampshire
New Jersey
New Mexico
New York
North Carolina
North Dakota
Ohio
Oklahoma
Oregon
Pennsylvania
Rhode Island
South Carolina
South Dakota
Tennessee
Texas
Utah
Vermont
Virginia
Washington
West Virginia
Wisconsin
Wyoming
9c. If vaccine was administered in canada which province was it administered in?
Alberta
British Columbia
Manitoba
New Brunswick
Newfoundland and Labrador
Northwest Territories
Nova Scotia
Nunavut
Ontario
Prince Edward Island
Quebec
Saskatchewan
Yukon
10. How many doses of vaccine were administered?
1
2
3
4
More than 4
11. If more than one dose was taken, were they the same vaccine eg. from the same manufacturer?
Yes
No
12. If more than one dose was taken, which vaccines were they eg. Who were the different manufacturers?
Astra Zeneca
Pfizer – BioNTech
Moderna
Johnson and Johnson
Other
If Selected Others Please Specify
13. When was the first dose of vaccine given?
14. When was the second dose of vaccine given?
15. When was the third dose of vaccine given?
16. When was the fourth dose of vaccine given?
17. When was the fifth dose of vaccine given?
18. When was the sixth dose of vaccine given?
19. When was the seventh dose of vaccine given?
20. Did the patient have any pre-existing conditions at the time that the vaccine was given?
Diabetes mellitus Type 1 (eg. Insulin needed every day)
Diabetes mellitus Type 2
Heart disease
History of Stroke
Hypertension
Asthma
chronic lung disease
chronic kidney disease
obesity
weakened immune system
neurologic disorder
epilepsy
Autoimmune disease
Other
If Selected Others Please Specify
21. When did the adverse reaction begin?
22. Did the adverse reaction resolve?
Yes
No
23. If the adverse reaction resolved, when did this happen?
24. Is the adverse event getting worse?
Yes
No
25. What side effects were experienced?
Allergic or allergic-type events
Allergic or allergic-type events
Anaphylaxis
Swelling of the lips
Swelling of the face/eyes
Swelling of the airway
Swelling of the tongue
Rash – Generalized
Rash - Localized
Itchy rash
Hives (bumps on the skin that can often be very itchy)
Increased heart rate
Loss of consciousness
Infection/syndrome/disease
Diabetes Mellitus Type 1 new
Diabetes Mellitus Type 1 -worsening
Diabetes Mellitus Type 2 new
Diabetes Mellitus Type 2 worsening
Kidney Failure new
Kidney failure worsening
Liver disease
Pancreatitis
Ischemic bowel disease
Gastrointestinal disease
Kawasaki Disease
Capillary leak syndrome
Guillain-barre syndrome
Bell’s palsy (facial paralysis)
Shingles
Herpes
Heart Disease
Myocarditis (inflammation of the heart muscle)
Pericarditis (inflammation of the lining
Increased heart rate
Gynecologic and pregnancy
Menstrual disorder
Abortion
Miscarriage
Still Birth
Birth Defect
Post-Menopausal Bleeding
Neurologic/Brain
Rheumatoid Arthritis
Lupus
Crohn’s Disease
Stroke
Bleeding in the brain
Brain fog
Loss of balance
Visual disturbance
Headaches and migraines
Central cerebral veinous thrombosis (blood clot in central veins of the brain)
Cancer
New cancer
Cancer Recurrence
Accelerated Progression of Pre-Existing Conditions
Blood Clots
Deep vein thrombosis
Fever
Abdominal pain
Vomiting
Diarrhea
Chills
Fatigue
Pain at injection site
Loss of consciousness
Sudden low blood pressure
Sneezing
Coughing
Difficulty breathing
New autoimmune disease
Worsening of pre-existing autoimmune disease
Hypoxia
Pulmonary embolism
Anemia
Thrombocytopenia (low platelets)
Others
If Selected Others Please Specify
26. What is the patient’s outcome?
Hospitalized in Intensive Care Unit (ICU)
Hospitalized not in Intensive Care Unit (ICU)
Not hospitalized
Recovered
Not recovered but improving
Not Recovered and getting worse
Not recovered but staying the same
Death
Unknown
27. How soon after the vaccine did the side effects occur?
Day 0
Day 1
Day 2
Day 3
Day 4
Day 5
Day 6
Other
If Selected Others Please Specify
28. Were any laboratory tests done?
Yes
No
29. How was the reaction treated?
Submit