Cefuroxime 1.5 g powder for solution for injection/infusion Ireland - English - HPRA (Health Products Regulatory Authority)

cefuroxime 1.5 g powder for solution for injection/infusion

fresenius kabi deutschland gmbh - cefuroxime sodium - powder for solution for injection/infusion - 1.5 gram(s) - second-generation cephalosporins; cefuroxime

CEFUROXIME AND DEXTROSE injection, solution United States - English - NLM (National Library of Medicine)

cefuroxime and dextrose injection, solution

b. braun medical inc. - cefuroxime sodium (unii: r8a7m9my61) (cefuroxime - unii:o1r9fj93ed) - cefuroxime for injection usp and dextrose injection usp is indicated for the treatment of patients with infections caused by susceptible strains of the designated organisms in the following diseases: - lower respiratory tract infections, including pneumonia, caused by streptococcus pneumoniae, haemophilus influenzae (including ampicillin-resistant strains), klebsiella spp., staphylococcus aureus (penicillinase- and non-penicillinase-producing strains), streptococcus pyogenes, and escherichia coli . - urinary tract infections caused by escherichia coli and klebsiella spp. - skin and skin-structure infections caused by staphylococcus aureus (penicillinase- and non-penicillinase-producing strains), streptococcus pyogenes, escherichia coli, klebsiella spp., and enterobacter spp. - septicemia caused by staphylococcus aureus (penicillinase- and non-penicillinase-producing strains), streptococcus pneumoniae, escherichia coli, haemophilus influenzae (including ampicillin-resistant strains), and kle

CEFUROXIME AXETIL- cefuroxime axetil tablet United States - English - NLM (National Library of Medicine)

cefuroxime axetil- cefuroxime axetil tablet

a-s medication solutions - cefuroxime axetil (unii: z49qdt0j8z) (cefuroxime - unii:o1r9fj93ed) - cefuroxime 250 mg - cefuroxime axetil tablets are indicated for the treatment of adult patients and pediatric patients (13 years and older) with mild-to-moderate pharyngitis/tonsillitis caused by susceptible strains of streptococcus pyogenes. limitations of use - the efficacy of cefuroxime axetil in the prevention of rheumatic fever was not established in clinical trials. - the efficacy of cefuroxime axetil in the treatment of penicillin-resistant strains of streptococcus pyogenes has not been demonstrated in clinical trials. cefuroxime axetil tablets are indicated for the treatment of pediatric patients (who can swallow tablets whole) with acute bacterial otitis media caused by susceptible strains of streptococcus pneumoniae , haemophilus influenzae (including β-lactamase–producing strains), moraxella catarrhalis (including β-lactamase–producing strains), or streptococcus pyogenes . cefuroxime axetil tablets are indicated for the treatment of adult and pediatric patients (13 years and older) with mild-to-moderate acute bacte

CEFUROXIME AXETIL tablet, film coated United States - English - NLM (National Library of Medicine)

cefuroxime axetil tablet, film coated

a-s medication solutions - cefuroxime axetil (unii: z49qdt0j8z) (cefuroxime - unii:o1r9fj93ed) - cefuroxime 250 mg - cefuroxime axetil tablets are indicated for the treatment of adult patients and pediatric patients (13 years and older) with mild-to-moderate pharyngitis/tonsillitis caused by susceptible strains of streptococcus pyogenes . limitations of use - the efficacy of cefuroxime axetil in the prevention of rheumatic fever was not established in clinical trials. -  the efficacy of cefuroxime axetil in the treatment of penicillin-resistant strains of streptococcus pyogenes has not been demonstrated in clinical trials. cefuroxime axetil tablets are indicated for the treatment of pediatric patients (who can swallow tablets whole) with acute bacterial otitis media caused by susceptible strains of streptococcus pneumoniae, haemophilus influenzae (including β-lactamase–producing strains), moraxella catarrhalis (including β-lactamase–producing strains), or streptococcus pyogenes . cefuroxime axetil tablets are indicated for the treatment of adult and pediatric patients (13 years and older) with mild-to-moderate acute ba

CEFUROXIME FOR INJECTION, USP POWDER FOR SOLUTION Canada - English - Health Canada

cefuroxime for injection, usp powder for solution

fresenius kabi canada ltd - cefuroxime (cefuroxime sodium) - powder for solution - 750mg - cefuroxime (cefuroxime sodium) 750mg - second generation cephalosporins

CEFUROXIME FOR INJECTION, USP POWDER FOR SOLUTION Canada - English - Health Canada

cefuroxime for injection, usp powder for solution

fresenius kabi canada ltd - cefuroxime (cefuroxime sodium) - powder for solution - 1.5g - cefuroxime (cefuroxime sodium) 1.5g - second generation cephalosporins

CEFUROXIME FOR INJECTION, USP POWDER FOR SOLUTION Canada - English - Health Canada

cefuroxime for injection, usp powder for solution

fresenius kabi canada ltd - cefuroxime (cefuroxime sodium) - powder for solution - 7.5g - cefuroxime (cefuroxime sodium) 7.5g - second generation cephalosporins

Cefuroxime Injection New Zealand - English - Medsafe (Medicines Safety Authority)

cefuroxime injection

novartis new zealand ltd - cefuroxime sodium 1577.8mg equivalent to cefuroxime 1500 mg - powder for injection - 1.5 g - active: cefuroxime sodium 1577.8mg equivalent to cefuroxime 1500 mg

Cefuroxime Injection New Zealand - English - Medsafe (Medicines Safety Authority)

cefuroxime injection

novartis new zealand ltd - cefuroxime sodium 788.9mg equivalent to cefuroxime 750 mg - powder for injection - 750 mg - active: cefuroxime sodium 788.9mg equivalent to cefuroxime 750 mg