Oftaquix is used to treat bacterial infections. To reduce the development of drug-resistant bacteria and maintain the effectiveness of Oftaquix and other antibacterial drugs, Oftaquix should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. Oftaquix Tablets/Injection and Oral Solution are indicated for the treatment of adults (≥18 years of age) with mild, moderate, and severe infections caused by susceptible strains of the designated microorganisms in the conditions listed in this section. Oftaquix Injection is indicated when intravenous administration offers a route of administration advantageous to the patient (e.g., patient cannot tolerate an oral dosage form). The FDA approved Oftaquix 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:
Meixil,
Amosine,
Renor,
Telviran,
Acimed,
Refluyet,
Eselan,
Lovrak,
Keflex,
Pidogrel,
Finpecia,
Sequinan,
Pantorc,
Gynotran,
Ciprager,
Elequine,
Linaris,
Cleron,
Metryl,
Prazidec,
Axodin,
Avorax,
Ilsatec,
Neuropen,
Fubenzon,
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Recognition versus adaptive up-regulation and degradation of CC chemokines by the chemokine decoy receptor D6 are determined by their N-terminal sequence. Thus, our data indicate that RAP55 is important for the assembly of cytoplasmic mRNP granules and that PRMT1 is required for RAP55A to localize to P-bodies. The adecur terazosina 2 mg results indicate that the major pharmacological and evolutionary difference between tachykinin-related agonists for insect (STKR) and human (NK1 and NK2) receptors resides in the C-terminal amino acid residues (R versus M).
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