New Zealand - English - Medsafe (Medicines Safety Authority)

roche products (nz) ltd - fleroxacin 4 mg/ml - solution for infusion - 400 mg - active: fleroxacin 4 mg/ml

New Zealand - English - Medsafe (Medicines Safety Authority)

roche products (nz) ltd - fleroxacin 200mg - tablet - 200 mg - active: fleroxacin 200mg

New Zealand - English - Medsafe (Medicines Safety Authority)

roche products (nz) ltd - fleroxacin 400mg - tablet - 400 mg - active: fleroxacin 400mg

Nigeria - English - NAFDAC (National Agency for Food and Drugs Administration and Control)

fleroxacin 200mg, 400mg

Nigeria - English - NAFDAC (National Agency for Food and Drugs Administration and Control)

fleroxacin 400mg/100ml

Australia - English - Department of Health (Therapeutic Goods Administration)

aspen pharma pty ltd - warfarin sodium -

Australia - English - Department of Health (Therapeutic Goods Administration)

aspen pharma pty ltd - warfarin sodium -

United States - English - NLM (National Library of Medicine)

redpharm drug inc. - ciprofloxacin hydrochloride (unii: 4ba73m5e37) (ciprofloxacin - unii:5e8k9i0o4u) - ciprofloxacin hydrochloride 500 mg - ciprofloxacin tablets usp are indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the conditions and patient populations listed below. please see dosage and administration for specific recommendations. urinary tract infections caused by escherichia coli , klebsiella pneumoniae , enterobacter cloacae , serratia marcescens , proteus mirabilis , providencia rettgeri , morganella morganii , citrobacter diversus , citrobacter freundii , pseudomonas aeruginosa , methicillin-susceptible staphylococcus epidermidis , staphylococcus saprophyticus , or enterococcus faecalis . acute uncomplicated cystitis in females caused by escherichia coli or staphylococcus saprophyticus . chronic bacterial prostatitis caused by escherichia coli or proteus mirabilis. lower respiratory tract infections caused by escherichia coli, klebsiella pneumoniae, enterobacter cloacae, proteus mirabilis, pseudomonas aeruginosa, haemophilus influenzae, haemophilus parainfluenzae, or

United States - English - NLM (National Library of Medicine)

direct rx - levofloxacin (unii: 6gnt3y5lmf) (levofloxacin anhydrous - unii:rix4e89y14) - levofloxacin anhydrous 750 mg - levofloxacin tablets are indicated for the treatment of adults (≥18 years of age) with mild, moderate, and severe infections caused by susceptible isolates of the designated microorganisms in the conditions listed in this section. 1.1 nosocomial pneumonia levofloxacin is indicated for the treatment of nosocomial pneumonia due to methicillin-susceptible staphylococcus aureus, pseudomonas aeruginosa, serratia marcescens, escherichia coli, klebsiella pneumoniae, haemophilus influenzae, or streptococcus pneumoniae. adjunctive therapy should be used as clinically indicated. where pseudomonas aeruginosa is a documented or presumptive pathogen, combination therapy with an anti-pseudomonal β-lactam is recommended [see clinical studies (14.1)]. 1.2 community-acquired pneumonia: 7 to 14 day treatment regimen levofloxacin is indicated for the treatment of community-acquired pneumonia due to methicillin-susceptible staphylococcus aureus, streptococcus pneumoniae (including multi-drug-resistant streptococcus pneumoniae [

Australia - English - Department of Health (Therapeutic Goods Administration)

generic health pty ltd - ciprofloxacin, quantity: 500 mg - tablet, film coated - excipient ingredients: maize starch; microcrystalline cellulose; sodium starch glycollate; colloidal anhydrous silica; magnesium stearate; hypromellose; purified talc; macrogol 4000; titanium dioxide - ciprofloxacin is indicated for the treatment of infections caused by susceptible organisms in the conditions listed below:,? urinary tract infections; ? gonorrhoeal urethritis and cervicitis; ? gastroenteritis; ? bronchial infections; ? skin and skin structure infections; ? bone and joint infections; ? chronic bacterial prostatitis of mild to moderate severity. inhalational anthrax (post-exposure): to reduce the incidence or progression of disease following exposure to aerosolised bacillus anthracis. ciprofloxacin serum concentrations achieved in humans serve as a surrogate endpoint reasonably likely to predict clinical benefit and provide the basis for this indication.,note: 1. typhoid and paratyphoid infections and infections due to multi-resistant staphylococcus aureus are excluded from the above due to insufficient data. 2. because gram-positive organisms are generally less sensitive to ciprofloxacin, it may not be the drug of choice in cases with gram-positive infections, such as pneumonia due to strepto