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  2. Cefoperazone - Wikipedia

    en.wikipedia.org/wiki/Cefoperazone

    Cefoperazone contains an N-methylthiotetrazole (NMTT or 1-MTT) side chain.As the antibiotic is broken down in the body, it releases free NMTT, which can cause hypoprothrombinemia (likely due to inhibition of the enzyme vitamin K epoxide reductase) and a reaction with ethanol similar to that produced by disulfiram (Antabuse effect), due to inhibition of aldehyde dehydrogenase.

  3. Cefoperazone/sulbactam - Wikipedia

    en.wikipedia.org/wiki/Cefoperazone/sulbactam

    Cefoperazone/sulbactam is a combination drug used as an antibiotic. It is effective for the treatment of urinary tract infections . [ 2 ] It contains cefoperazone , a β-lactam antibiotic , and sulbactam , a β-lactamase inhibitor , which helps prevent bacteria from breaking down cefoperazone.

  4. ATC code J01 - Wikipedia

    en.wikipedia.org/wiki/ATC_code_J01

    ATC code J01 Antibacterials for systemic use is a therapeutic subgroup of the Anatomical Therapeutic Chemical Classification System, a system of alphanumeric codes developed by the World Health Organization (WHO) for the classification of drugs and other medical products.

  5. Sulbactam - Wikipedia

    en.wikipedia.org/wiki/Sulbactam

    The combination cefoperazone/sulbactam (Sulperazon) is available in many countries but not in the United States. [ 4 ] The co-packaged combination sulbactam/durlobactam was approved for medical use in the United States in May 2023.

  6. Cefbuperazone - Wikipedia

    en.wikipedia.org/wiki/Cefbuperazone

    This systemic antibiotic -related article is a stub. You can help Wikipedia by expanding it.

  7. Cefprozil - Wikipedia

    en.wikipedia.org/wiki/Cefprozil

    Cefprozil is a second-generation cephalosporin antibiotic. [1] Originally discovered in 1983, and approved in 1992, [2] it was sold under the tradename Cefzil by Bristol Meyers Squibb until 2010 when the brand name version was discontinued. [3]

  8. Cefuroxime - Wikipedia

    en.wikipedia.org/wiki/Cefuroxime

    Cefuroxime is active against many bacteria including susceptible strains of Staphylococci and Streptococci, as well as a range of gram negative organisms. [11] As with the other cephalosporins, it is susceptible to beta-lactamase, although as a second-generation variety, it is less so.

  9. Cefmetazole - Wikipedia

    en.wikipedia.org/wiki/Cefmetazole

    The chemical structure of cefmetazole, like that of several other cephalosporins, contains an N-methylthiotetrazole (NMTT or 1-MTT) side chain.As the antibiotic is broken down in the body, it releases free NMTT, which can cause hypoprothrombinemia (likely due to inhibition of the enzyme vitamin K epoxide reductase) and a reaction with ethanol similar to that produced by disulfiram, due to ...