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11-18-2015 05:37 AM |
Quote:
Originally Posted by NECHFalcon68
(Post 1147114)
Having been in the vaccine business, I can tell you that if there was an improper mix of one batch, it would be grounds for recall.
If enough adverse events are reported to the FDA, they will require an investigation and possible market action (recall) if warranted.
I had my shot yesterday (first one in about 20 years, because my doctor insisted on it) and felt no effects today. It was however, not the high dose...as I have not hit that magic age yet.
BTW, the flu strains to be cultivated for vaccines are decided in January by the CDC/FDA, 9 months before the season starts, so that the manufacturers will have enough time to fully culture and gear up for mass production. Unfortunately, it is a well-educated and professional guess for the strains, and the typical clinical trials may not be performed....and the process is a little more complex than what you saw with Dustin Hoffman in "Contagion"
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NECH Falcon:
I agree with and respect your opinion because this was your profession and hence I would defer to your knowledge. I have great respect for the FDAbut it would seem that in order for a recall to take place often not always there has to be a reason cited for it, which usually means someone was affected the same as food borne illnesses, same with cars, toys, etc and then the recall
Since the flu shot has only an efficacy of three months I get my vaccination as late as possible . Again I believe that if a person has compromised immune system s/he may want to avoid the high dose or at least consult their doc as to what dosage to accept
Please Best Regards:
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