“…The drug acts as a noncompetitive inhibitor of the DNA pol enzymatic activity by binding directly to its pyrophosphate binding site and blocking the cleavage of pyrophosphate from the nucleoside triphosphate, thus impeding further elongation of the viral DNA (Arduino & Porter, 2008;Piret & Boivin, 2011;Poole & James, 2018). Studies in HIV positive individuals and HSCT recipients, including isolated cases reports as well as randomized phase II trials, show that intravenous administration of FOS is effective in treating severe ACVr HSV-1 and -2 mucocutaneous lesions, since it reduces viral shedding along with the size and duration of lesions (Chatis et al, 1989;Iino et al, 1996;MacPhail et al, 1989;Naik et al, 1995;Sall et al, 1989;Verdonck et al, 1993), being more efficacious and showing less toxicity compared to vidarabine (Safrin et al, 1991). A few reports have also shown good results using FOS cream 1%-2.4% for the treatment of orogenital and cutaneous ACVr HSV lesions (Heidenreich et al, 2020;Javaly et al, 1999;Pechère et al, 1998; Table 1).…”