Live-saving antibacterial for severe abdominal sepsis and peritonitis. For severe surgical infections and use in surgical oncology.
Taurolidine, the active substance of Taurolin®, is derived from the naturally occurring endogenous aminosulphonic acid taurine.
Active against aerobic and anaerobic, gram-positive and gram-negative bacteria, mycobacteria, and fungi (prevents secondary Candida colonization). Prevents adherence of microorganisms. Bacterial resistance unlikely to occur due to unique mechanism of action. Active against MRSA, ORSA, VRE, VISA, and VRSA.

E. coli (magnification 15"000x) before Taurolin®-Exposition

E. coli (magnification 15"000x) afterTaurolin®-Exposition
Very low toxicity. LD50 in all species and with all applications far above 1,000 mg/kg BW.
No mutagenic, embryotoxic, or teratogenic effects and no cytotoxicity or ototoxicity.
No general pharmacological and pharmacodynamical actions. Favourable clinical safety profile based on experience with aprox. 14,000 patients, well established for local i.p. and experimental i.v. treatment of abdominal sepsis, peritonitis and pancreatitis, catheter sepsis, osteitis and prevention of adherence and growth of tumor metastases.
Only minor local and no systemic clinically relevant adverse events after correct administration.
Compatible with many parenterals.
Can be combined with all conventional antibiotics.
Reduces mortality and morbidity in patients with surgical infections, abdominal sepsis and peritonitis. Prevents adherence and growth of metastases and stops or reduces tumor progression. Practically no adverse events.