2012
DOI: 10.5799/ahinjs.02.2012.03.0049
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Clinical profile of patients treated with cefepime/tazobactam: A new ß-lactam/ß-lactamase inhibitor combination

Abstract: Objectives: Cefepime/tazobactam is a new ß-lactam/ß-lactamase inhibitor combination licensed for clinical use by Drugs Controller General of India. Aim of our study was to analyze the clinical efficacy and safety of cefepime/tazobactam in patients with sepsis. To the best of our knowledge, this is the first published clinical study on this drug. Materials and methods:A retrospective observational study on the efficacy and safety of cefepime/tazobactam was conducted at a tertiary care hospital, South India. Pat… Show more

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Cited by 13 publications
(10 citation statements)
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“…Several reports suggest that B-lactam/B-lactamase inhibitors (BL/BLI) combinations like cefoperazone–sulbactam, piperacillin–tazobactam and ampicillin–sulbactam can be used as suitable options for treating less severe cases, 6 , 7 whereas carbapenems can be used as reserve drug for more severe cases.…”
Section: Introductionmentioning
confidence: 99%
“…Several reports suggest that B-lactam/B-lactamase inhibitors (BL/BLI) combinations like cefoperazone–sulbactam, piperacillin–tazobactam and ampicillin–sulbactam can be used as suitable options for treating less severe cases, 6 , 7 whereas carbapenems can be used as reserve drug for more severe cases.…”
Section: Introductionmentioning
confidence: 99%
“…TAZ is semi-synthetic parenteral penicillin. It is a β-lactamase inhibitor with a broad spectrum of antibacterial activity against most gram positive, gram negative aerobic and anaerobic bacteria (Ghafur, Ashwini, Priyadarshini, 2012.). Chemically, it is known as (2S,3S,5R)-3-methyl-7oxo-3-(1H-1,2,3-triazol-1-ylmethyl)-4-thia-1-azabicyclo [3.2.0] heptane-2-carboxylic acid 4, 4-dioxide ( Figure 2).…”
Section: Introductionmentioning
confidence: 99%
“…Inadequate access to such novel MDR and active therapies in countries such as India and China, coupled with a significant compromise in the effectiveness of older BL-BLIs, has resulted in a crippling therapeutic void in the treatment of contemporary Gram-negative infections (9,(19)(20)(21)(22). Meanwhile, indigenous pharmaceutical firms in these countries resorted to marketing several unorthodox BL-BLI combinations, namely, ceftriaxone-tazobactam, ceftazidime-tazobactam, cefoperazone-tazobactam, cefepime-tazobactam, cefotaxime-sulbactam, ceftazidime-sulbactam, ceftriaxone-sulbactam, cefepime-sulbactam, and meropenemsulbactam (Table 1) (9,(23)(24)(25)(26)(27). The doses of the BLIs in all these combinations were retained at the same ratios used in the older scientifically developed combinations, such as piperacillin-tazobactam and ampicillin-sulbactam.…”
mentioning
confidence: 99%