Eravacycline: a comprehensive review of in vitro activity, clinical efficacy, and real-world applications.

Eravacycline, a synthetic fluorocycline, belongs to the tetracyclines class with a basic chemical structure, and specific modifications were introduced on the D ring of the naphtacen nucleus. Similar to other tetracycline, eravacycline exerts its antibacterial action by reversibly binding to the bacterial ribosomal 30S subunit, preventing the incorporation of amino acid residues into elongating peptide chains and ultimately disrupting bacterial protein synthesis. Eravacycline demonstrates potent in vitro activity against many Gram-positive and Gram-negative aerobes, anaerobes, and multidrug-resistant organisms. Randomized controlled trials and its associated meta-analysis affirms eravacycline's efficacy in treating complicated intra-abdominal infections. Moreover, real-world studies showcase eravacycline's adaptability and effectiveness in diverse clinical conditions, emphasizing its utility beyond labeled indications. Despite common gastrointestinal adverse events, eravacycline maintains an overall favorable safety profile, reinforcing its status as a tolerable antibiotic. However, ongoing research is essential for refining eravacycline's role, exploring combination therapy, and assessing its performance against biofilms, contributing to its continued success in combating challenging bacterial infections.