Most meningococcal serogroups A, B and C; Shigella spp., Escherichia coli resistant to sulfonamides.
Due to the bacteriostatic effect, intense immunity is required to kill the pathogen.
The most active preparations with heterocyclic aromatic substituents (sulfamethoxazole, sulfadiazine, sulfafurazole, etc.).
Due to widespread resistance, severe side effects and the development of new more effective antimicrobial agents, sulfonamides in monotherapy are practically not used (except for sulfacetamide for topical use).
In order to prevent crystalluria during the treatment period, an abundant drink (2-3 liters per day) is necessary, the risk of crystalluria can be reduced by basifying urine.
When rashes appear, treatment should be discontinued because of the danger of developing serious allergic reactions like Stevens-Johnson syndrome.
It may be necessary to monitor blood and urine tests, especially with prolonged treatment.
All sulfonamides have a high degree of binding to proteins, each of them has a different ability to displace indirect bilirubin.
All sulfonamides have a wide spectrum of action, but due to the wide spread of resistance their use is limited, sensitivity to them varies widely, even in potentially sensitive pathogens. Acquired resistance to sulfonamides is widespread among previously sensitive microorganisms - Neisseria spp., Shigella spp. and other enterobacteria, as well as staphylococci and streptococci. High-level stability is usually constant and irreversible. There is complete mutual stability between all sulfonamides.