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  2. Levofloxacin - Wikipedia

    en.wikipedia.org/wiki/Levofloxacin

    Levofloxacin, sold under the brand name Levaquin among others, is a broad-spectrum antibiotic of the fluoroquinolone drug class. [6] It is the left-handed isomer of the medication ofloxacin .

  3. Cinoxacin - Wikipedia

    en.wikipedia.org/wiki/Cinoxacin

    The usual adult dosage for the treatment of urinary tract infections is 1 gram daily, administered orally in two or four divided doses (500 mg b.i.d. or 250 mg q.i.d. respectively) for seven to 14 days.

  4. List of antibiotics - Wikipedia

    en.wikipedia.org/wiki/List_of_antibiotics

    The following is a list of antibiotics.The highest division between antibiotics is bactericidal and bacteriostatic.Bactericidals kill bacteria directly, whereas bacteriostatics prevent them from dividing.

  5. Dexamethasone/levofloxacin - Wikipedia

    en.wikipedia.org/wiki/Dexamethasone/levofloxacin

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us

  6. Quinolone antibiotic - Wikipedia

    en.wikipedia.org/wiki/Quinolone_antibiotic

    In a study comparing the safety and efficacy of levofloxacin to that of azithromycin or ceftriaxone in 712 children with community-acquired pneumonia, serious adverse events were experienced by 6% of those treated with levofloxacin and 4% of those treated with comparator antibiotics. Most of these were considered by the treating physician to be ...

  7. Category:Fluoroquinolone antibiotics - Wikipedia

    en.wikipedia.org/wiki/Category:Fluoroquinolone...

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  8. Ofloxacin - Wikipedia

    en.wikipedia.org/wiki/Ofloxacin

    Ofloxacin is a racemic mixture, which consists of 50% levofloxacin (the biologically active component) and 50% of its “mirror image” or enantiomer dextrofloxacin. [52] "After multiple-dose administration of 200 mg and 300 mg doses, peak serum levels of 2.2 and 3.6 μg/ml, respectively, are predicted at steady-state.

  9. Ciprofloxacin - Wikipedia

    en.wikipedia.org/wiki/Ciprofloxacin

    These tablets contain 35% of the administered dose in an immediate-release form and 65% in a slow-release matrix. Maximum serum concentrations are achieved between 1 and 4 hours after administration. Compared to the 250- and 500-mg immediate-release tablets, the 500-mg and 1000-mg XR tablets provide higher C max, but the 24‑hour AUCs are ...

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