“…As the BNT162b2 mRNA vaccine uses lipid nanoparticles as carrier vehicles instead of an adenoviral vector, it is not known to be associated with VITT. Multiple surveillance studies from Israel [25], Scotland [36,41], France [30], Denmark [29], Hong Kong [34], the UK [24,27,32,38], and the USA [33] noted no significant association between BNT162b2 and VITT-related adverse events, such as cerebral venous sinus thrombosis (CVST), splanchnic vein thrombosis, deep vein thrombosis (DVT), pulmonary embolism, venous and arterial thromboembolism, immune thrombocytopenia, disseminated intravascular coagulation, and subarachnoid hemorrhage (Table 4). overlapped substantially with that of the negative control (i.e., lower limb fracture), in cating that certain confounders were at play [44].…”