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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. Abbrev. [1]Meaning [1] Latin (or Neo-Latin) origin [1]; a.c. before meals: a.d., ad, AD right ear auris dextra a.m., am, AM morning: ante meridiem: nocte every night ...

  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. Cefamandole - Wikipedia

    en.wikipedia.org/wiki/Cefamandole

    Cefamandole (INN, also known as cephamandole) is a second-generation broad-spectrum cephalosporin antibiotic.The clinically used form of cefamandole is the formate ester cefamandole nafate, a prodrug which is administered parenterally.

  7. Cefbuperazone - Wikipedia

    en.wikipedia.org/wiki/Cefbuperazone

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

  8. Ceftazidime/avibactam - Wikipedia

    en.wikipedia.org/wiki/Ceftazidime/avibactam

    For many bacterial infections, it offers little or no advantage over ceftazidime monotherapy, due to the widespread expression of resistance mechanisms other than β-lactamase production.

  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 ...