Again, just because an adverse event occurs does not mean it is assumed to be due to the medicine. Nevertheless, reporting is encouraged. You don’t need a survey, the mechanisms are already in place for reporting.
This one was discussed at one of our meetings.
Elderly female got booster.
Went home.
Then went out shopping.
On way to car tripped and fell
Fractured pelvis.
Died a week later
Daughter blaming the jab.
Death due to booster?
Or this actual patient:
Young fella got 2nd mRNA jab. A week later got abdominal pain. This went on for several days - pain waxed and waned. Parents worried he got a reaction to the jab. The surgeons took out an infected appendix. Parents did think that the Covid jab put in train the events that lead to appendicitis and are blaming the jab.
Or this one:
Young fella got booster and Then Covid positive 3 months ago. Then developed unexplained abdominal pain. All scans and investigations negative. Still has pain. Parents are blaming the Jab.
Basically all 3 can be reported to TGA - and when it’s reported will be 3 adverse events .