In light of the fact that the SA Health Products Regulatory Authority (SAHPRA) is said to not have known about the report that the Food and Drug Administration received from Pfizer and used to authorise the vaccines, (a) which report and evidence was utilised by SAHPRA to determine the safety of Pfizer, (b) was it inclusive of the recently publicised report on the adverse effects of the vaccine and (c) was SAHPRA aware of the possible side effects and adverse effects of the Pfizer vaccine?