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      FDA approved antibacterial drugs: 2018-2019

      review-article
      1 , 2 , 3 , * , 1 , 2 , 2 , 4
      Discoveries
      Applied Systems srl
      FDA approved drugs, Plazomicin, Eravacycline, Sarecycline, Omadacycline. Rifamycin, Imipenem, Cilastatin and Relebactam, Pretomanid, Lefamulin, Cefiderocol, 2018, 2019.

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          Abstract

          Bacterial resistance to existent antibiotherapy is a perpetual internationally-recognized problem. Year after year, there is a continuous need for novel antibacterial drugs and this research and development efforts recently resulted in few new drugs or combination of drugs proposed for the use into the clinic. This review focuses on the novel US FDA approved antibacterial agents in the last two years (2018-2019). Plazomicin, eravacycline, sarecycline, omadacycline, rifamycin (2018) and imipenem, cilastatin and relebactam combination, pretomanid, lefamulin, cefiderocol (2019) are new therapeutic options. Plazomicin aminoglycoside antibiotic targets Enterobacteriaceae infections, being mainly used for the complicated urinary tract infections. The fully synthetic fluorocycline eravacycline gained approval for the complicated intra-abdominal infections. The tetracycline-derived antibiotic sarecycline might be a useful strategy for the management of non-nodular moderate to severe acne, while the other tetracycline-derived antibiotic approved, omadacycline, may be used for the patients with acute bacterial skin and skin structure infections and community-acquired bacterial pneumonia. The already-known RNA-synthesis suppressor rifamycin is now also approved for noninvasive Escherichia Coli-caused travelers' diarrhea. Two combinatorial strategies were approved for complicated urinary tract infections, complicated intra-abdominal infections (imipenem, cilastatin and relebactam) and lung tuberculosis (pretomanid in combination with bedaquiline and linezolid). Lefamulin is a semisynthetic pleuromutilin antibiotic for community-acquired bacterial pneumonia, while cefiderocol, a cephalosporin antibiotic is the last antibacterial drug approved in 2019, for the use in complicated urinary tract infections. Despite of these new developments, there is an ongoing need and urgency to develop novel antibiotic strategies and drugs to overrun the bacterial resistance to antibiotics.

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          Most cited references53

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          Co-selection of multi-antibiotic resistance in bacterial pathogens in metal and microplastic contaminated environments: An emerging health threat

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            In Vitro Antibacterial Properties of Cefiderocol, a Novel Siderophore Cephalosporin, against Gram-Negative Bacteria

            ABSTRACT Cefiderocol (CFDC; S-649266), a novel parenteral siderophore cephalosporin conjugated with a catechol moiety, has a characteristic antibacterial spectrum with a potent activity against a broad range of aerobic Gram-negative bacterial species, including carbapenem-resistant strains of Enterobacteriaceae and nonfermenting bacteria such as Pseudomonas aeruginosa and Acinetobacter baumannii. Cefiderocol has affinity mainly for penicillin-binding protein 3 (PBP3) of Enterobacteriaceae and nonfermenting bacteria similar to that of ceftazidime. A deficiency of the iron transporter PiuA in P. aeruginosa or both CirA and Fiu in Escherichia coli caused 16-fold increases in cefiderocol MICs, suggesting that these iron transporters contribute to the permeation of cefiderocol across the outer membrane. The deficiency of OmpK35/36 in Klebsiella pneumoniae and the overproduction of efflux pump MexA-MexB-OprM in P. aeruginosa showed no significant impact on the activity of cefiderocol.
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              Cefiderocol: A Siderophore Cephalosporin with Activity Against Carbapenem-Resistant and Multidrug-Resistant Gram-Negative Bacilli

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                Author and article information

                Journal
                Discoveries (Craiova)
                Discoveries (Craiova)
                Discoveries (Craiova)
                Discoveries
                Applied Systems srl
                2359-7232
                31 December 2019
                Oct-Dec 2019
                : 7
                : 4
                : e102
                Affiliations
                [1]Department of Anesthesia and Intensive Care, Fundeni Clinical Institute, Bucharest, Romania
                [2]Carol Davila University of Medicine and Pharmacy, Bucharest, Romania
                [3]Université Paris Sud XI, Faculté de Médecine, Le Kremlin-Bicêtre, France
                [4]Dr. Davila Teaching Hospital of Nephrology, Bucharest, Romania
                Author notes
                Stefan Andrei, MD, Department of Anesthesia and Intensive Care, Fundeni Clinical Institute, 258 Soseaua Fundeni, Bucharest, 022328, Romania; Carol Davila University of Medicine and Pharmacy, Bucharest, Romania; Université Paris Sud XI, Faculté de Médecine, 63 Rue Gabriel Péri, 94270 Le Kremlin-Bicêtre, France; stefan.m.andrei@gmail.com
                Article
                212
                10.15190/d.2019.15
                7086080
                32309620
                bda5faee-3b98-4f64-866c-4c00de8ed3fe
                Copyright: © 2019, Andrei et al. and Applied Systems

                This article is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 29 December 2019
                : 31 December 2019
                : 31 December 2019
                Categories
                Focused Review

                fda approved drugs,plazomicin,eravacycline,sarecycline,omadacycline. rifamycin,imipenem,cilastatin and relebactam,pretomanid,lefamulin,cefiderocol,2018,2019.

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