The possibility of reducing the frequency, duration, and severity of acute respiratory infections (ARI) during the epidemic season in children with tuberculosis is an important component of a comprehensive approach to the treatment of the disease and its favorable outcome. In this regard, the anti-inflammatory drug ammonium glycyrrhizinate is of particular practical interest, as it has a successful experience of use during the ARI epidemic season in the pediatric patient population. Patients and methods. We observed 2 groups of patients (main (n = 44) and control (n = 32)) aged 3–17 years with various forms of respiratory tuberculosis during the ARI epidemic season. Patients in the main group, in addition to baseline therapy for the underlying disease, were prescribed ammonium glycyrrhizinate for 60 days. On days 1, 15, 30, 45, and 60 of observation, physical examination was performed; cases and duration of ARI, the volume of additionally required therapy, and cases of adverse reactions associated with the study drug were recorded. ARI symptoms were assessed using a 4-point scale. Results. Among patients receiving ammonium glycyrrhizinate, the frequency of ARI was recorded more than 2 times lower compared to the control group (15.9% vs 34.4%); 9.4% of children in the control group had ARI twice, while no recurrent ARI episodes were noted in the main group. The average duration of ARI in the main group was 3 days – 40% less compared to the control group (5 [4; 8] days, p = 0.008). In the group of patients receiving ammonium glycyrrhizinate, compared to the control group, ARI episodes occurred with a lower frequency of symptoms of weakness (40% vs 90%, p = 0.04), decreased appetite (6.7% vs 63.6%, p = 0.003), headache (13.3% vs 54.5%, p = 0.003); the duration of fever was significantly shorter (Me 2 [1; 2] vs 3 [3; 5] days (p = 0.014)). Regarding respiratory symptoms, the main group showed a tendency towards a higher frequency of daytime cough (40% vs 18.2%) along with a lower frequency of sputum (6.7% vs 27.3%) and nighttime cough (6.7% vs 9.1%), which was associated with the mucoregulatory effect of the drug. The mean score for weakness and decreased appetite in the main group was 0.5 ± 0.3 and 0.14 ± 0.01 points, respectively; in the control group, these symptoms were significantly more intense – 1.9 ± 0.7 and 1.3 ± 0.5 points, respectively (p < 0.05). Conclusion. The obtained results demonstrate the efficacy and safety of administering ammonium glycyrrhizinate to patients with respiratory tuberculosis during the ARI epidemic season in addition to baseline anti-tuberculosis therapy in order to reduce the frequency, duration, and intensity of ARI symptoms. Key words: children, tuberculosis, acute respiratory infection, ammonium glycyrrhizinate, cough, intoxication