Omadacycline is a semisynthetic tetracycline antibiotic. Phase III clinical trial results have shown that omadacycline has an acceptable safety profile in the treatment of acute bacterial skin and skin structure infections and community-acquired bacterial pneumonia. Similar to most tetracyclines, transient nausea and vomiting and low-magnitude increases in liver aminotransferases were the most frequent treatment-emergent adverse events in phase III studies but were not treatment limiting. Package insert warnings and precautions for omadacycline include tooth discoloration; enamel hypoplasia; inhibition of bone growth following use in late pregnancy, infancy, or childhood up to 8 years of age; an imbalance in mortality (2%, compared with 1% in moxifloxacin-treated patients) was observed in the phase III study in patients with community-acquired bacterial pneumonia. Omadacycline has no effect on the QT interval, and its affinity for muscarinic M2 receptors resulted in transient heart rate increases following dosing.
CITATION STYLE
Opal, S., File, T. M., Van Der Poll, T., Tzanis, E., Chitra, S., & McGovern, P. C. (2019). An Integrated Safety Summary of Omadacycline, a Novel Aminomethylcycline Antibiotic. Clinical Infectious Diseases, 69, S40–S47. https://doi.org/10.1093/cid/ciz398
Mendeley helps you to discover research relevant for your work.