Tetrachloromethane (CCl4) is a toxic chemical substance known in scientific research as a model for studying the damage of parenchymal liver cells. The mechanisms of CCl4 toxicity include the activation of lipid peroxidation processes, the intensive formation of free radicals, and, as a result, the disruption of the pro-/antioxidant balance. This work aimed to study the effect of the liposomal drug “Butaintersyl” on the activity of the glutathione antioxidant protection system and the intensity of lipid peroxidation processes in the blood of rats under conditions of toxic damage caused by tetrachloromethane. The studies were conducted on white sexually mature young Wistar rats weighing 180–200 g, kept in the institute's vivarium of the State Scientific Research Control Institute of Veterinary Drugs and Feed Additives. In the blood of the rats, changes in the activity of glutathione peroxidase and the level of reduced glutathione were studied, as well as the levels of lipid peroxidation products: lipid hydroperoxides and TBA-active products. The development of oxidative stress in the first experimental group of rats was accompanied by the suppression of the glutathione antioxidant protection system, as evidenced by a decrease in blood glutathione peroxidase activity and the level of reduced glutathione. At the same time, the intoxicated animals showed an increase in lipid peroxidation processes, namely an increase in the blood levels of lipid hydroperoxides and TBA-active products throughout the study period. The studies showed that in cases of poisoning of various origins, it is advisable to use drugs that reduce the formation of reactive oxygen species and lipoperoxidation processes, exhibit antioxidant effects, and stabilize cell membranes. A special place among such drugs is occupied by the liposomal drug “Butaintersyl”. This drug ensures the stabilization of biological membranes. The liposomal drug “Butaintersyl” contributed to suppressing lipid peroxidation processes and activating the antioxidant protection system, as evidenced by the high content of reduced glutathione and glutathione peroxidase activity. Due to its antioxidant properties, the drug positively affected the activity of membrane-dependent enzymes. It reduced the level of endogenous intoxication, allowing it to be recommended for inclusion in prevention schemes for toxic liver damage caused by chemical compounds.