Levofloxacinum is used to treat a variety of bacterial infections. This medication belongs to a class of drugs known as quinolone antibiotics. It works by stopping the growth of bacteria. This antibiotic treats only bacterial infections. It will not work for viral infections (such as common cold, flu). Using any antibiotic when it is not needed can cause it to not work for future infections. The FDA approved Levofloxacinum in December 1996. This medication may be available under multiple brand names and/or in several different forms.
Other names for this medication:
Levofloxacin,
Levaquin,
Armolev,
Auxxil,
Cravit,
Cravox,
Difloxin,
Elequine,
Glevo,
Iquix,
Leflox,
Lefloxin,
Leflumax,
Lequin,
Levobact,
Levocin,
Levocine,
Levoday,
Levoflox,
Levofloxacina,
Levofloxacino,
Levofloxacinum,
Levomac,
Levomax,
Levoquin,
Levoquinol,
Levores,
Levotac,
Levox,
Levoxa,
Levoxacin,
Levoxin,
Levozine,
Levunid,
Locin,
Lovequin,
Loxin,
Loxof,
Lufi,
Medibiox,
Mosardal,
Nevotek,
Nislev,
Novacilina,
Oftaquix,
Orlev,
Ovel,
Ovelquin,
Proxime,
Quantrum,
Quinobiot,
Quixin,
Recamicina,
Reskuin,
Tamiram,
Tavaloxx,
Tavanic,
Trevox,
Truxa,
Ultraquin,
Uniflox,
Volequin,
Voxin,
Similar Products:
Dolex,
Eszopiclone,
Relaxyl,
Tramagesic,
Turimycin,
Trandate,
Ulcepraz,
Securo,
Olsar,
Duloxetina,
Cymbalta,
Sortis,
Paroxetina,
Diagesic,
Clopivas,
Omnic,
Stemzine,
Quixin,
Zentius,
Uprox,
Tetramin,
Larotid,
Vonum,
Resta,
Clirbest,
Zevin,
Losec,
Anxionil,
Perten,
Vodelax,
Simgal,
Pyrodex,
Biogel,
Lanacine,
Simvastatin,
Evoclin,
Cibalgina,
Forcet,
Lofral,
Trifen,
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Activation of herpes specific antigens and infectious virus in a hamster cell line transformed by HSV-2. Congress approves FY 2000 budget, sets aside money for Medicare reform. Asymmetry of electroencephalographic (EEG) activity across the frontal regions of the 2 hemispheres (left minus right hemisphere activation) was used to index approach motivation. Cross-linking experiments revealed that the anchored proOmpA2xH1 that does not interact with either ketoprofen drug profile of amlodipine SecY or SecA. Thus, during ATP hydrolysis the COOH-terminal end of the conserved domain moves into a less polar environment, whereas the NH2-terminal end moves into a more hydrophilic environment as product is formed.
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