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Description
A 2mg DSIP vial requiring 20 draws experiences 20 puncture events
The population for the analysis of the primary efficacy endpoint included, 36,621 participants 12 years of age and older (18,242 in the Pfizer-BioNTech COVID-19 Vaccine group and 18,379 in the placebo group) who did not have evidence of prior infection with SARS-CoV-2 through 7 days after the second dose
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Consistent and verifiable batch numbering systems
doi: 10.1016/j.bbrc.2004.10.157
BPC-157 and TB-500 remain on the FDA Category 2 'do not compound' list
