Ireland - English - HPRA (Health Products Regulatory Authority)

amdipharm limited - cefixime trihydrate - film-coated tablet - third-generation cephalosporins; cefixime

Kenya - English - Pharmacy and Poisons Board

oriana limited p.o box 19528-00202, nairobi - cefixime trihydrate usp equiv. to cefixime and… - suspension and effervescent granules for oral - cefixime trihydrate usp equiv. to cefixime 50.00… - cefixime

Kenya - English - Pharmacy and Poisons Board

national pharmacy p.o box 17843- 00500, nairobi kenya - cefixime trihydrate usp. eq. to anhydrous cefixime - tablet - cefixime trihydrate usp. eq. to anhydrous… - cefixime

Kenya - English - Pharmacy and Poisons Board

doctor pharma kenya limited maxi tower building, muthithi road, westlands, p - cefixime trihydrate, potassium clavulanate - film-coated tablet - cefixime trihydrate 200mg, potassium clavulanate… - cefixime

Kenya - English - Pharmacy and Poisons Board

national pharmaceutical industries co. saoc p.o box 120, rusayl , postal code 124, sultanate - cefixime trihydrate equivalent to cefixime - tablet - each capsule contains cefixime 400mg - cefixime

Kenya - English - Pharmacy and Poisons Board

national pharmaceutical industries co. saoc p.o box 120, rusayl , postal code 124, sultanate - cefixime trihydrate equivalent to cefixime - capsule - each capsule contains cefixime 400mg - cefixime

Kenya - English - Pharmacy and Poisons Board

harleys limited 63 westland's road. - cefixime trihydrate usp - capsule - cefixime trihydrate 200mg - cefixime

Kenya - English - Pharmacy and Poisons Board

harley's limited 63 westlands road - cefixime trihydrate usp - capsule - cefixime trihydrate usp 200mg - cefixime

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

northstar rxllc - cefixime (unii: 97i1c92e55) (cefixime anhydrous - unii:xz7bg04gjx) - cefixime for oral suspension is indicated in the treatment of adults and pediatric patients six months of age or older with uncomplicated urinary tract infections caused by susceptible isolates of escherichia coli and proteus mirabilis . cefixime for oral suspension is indicated in the treatment of adults and pediatric patients six months of age or older with otitis media caused by susceptible isolates of  haemophilus influenzae , moraxella catarrhalis , and streptococcus pyogenes . (efficacy for streptococcus pyogenes in this organ system was studied in fewer than 10 infections.) note: for patients with otitis media caused by streptococcus pneumoniae , overall response was approximately 10% lower for cefixime than for the comparator. [ s ee c

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

remedyrepack inc. - cefixime (unii: 97i1c92e55) (cefixime anhydrous - unii:xz7bg04gjx) - cefixime for oral suspension and cefixime capsule is indicated in the treatment of adults and pediatric patients six months of age or older with uncomplicated urinary tract infections caused by susceptible isolates of escherichia coli and proteus mirabilis . cefixime for oral suspension and cefixime capsule is indicated in the treatment of adults and pediatric patients six months of age or older with otitis media caused by susceptible isolates of haemophilus influenzae , moraxella catarrhalis , and streptococcus pyogenes . (efficacy for streptococcus pyogenes in this organ system was studied in fewer than 10 infections.) note: for patients with otitis media caused by streptococcus pneumoniae , overall response was approximately 10% lower for cefixime than for the comparator [see clinical studies ( 14)] . cefixime for oral suspension and cefixime capsule is indicated in the treatment of adults and pediatric patients six months of age or older with pharyngitis and tonsillitis caused by susceptible isolates of streptococcus pyogenes. (note: penicillin is the usual drug of choice in the treatment of streptococcus pyogenes infections. cefixime for oral suspension and cefixime capsule is generally effective in the eradication of streptococcus pyogenes from the nasopharynx; however, data establishing the efficacy of cefixime for oral suspension and cefixime capsule in the subsequent prevention of rheumatic fever is not available.) cefixime for oral suspension and cefixime capsule is indicated in the treatment of adults and pediatric patients six months of age or older with acute exacerbations of chronic bronchitis caused by susceptible isolates of streptococcus pneumoniae and haemophilus influenzae . cefixime for oral suspension and cefixime capsule is indicated in the treatment of adults and pediatric patients six months of age or older with uncomplicated gonorrhea (cervical/urethral) caused by susceptible isolates of neisseria gonorrhoeae (penicillinase-and non-penicillinase-producing isolates). to reduce the development of drug resistant bacteria and maintain the effectiveness of cefixime and other antibacterial drugs, cefixime for oral suspension and cefixime capsule should be used only to treat 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 antimicrobial therapy. in the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. cefixime is contraindicated in patients with known allergy to cefixime or other cephalosporins. pregnancy category b . reproduction studies have been performed in mice and rats at doses up to 40 times the human dose and have revealed no evidence of harm to the fetus due to cefixime. there are no adequate and well-controlled studies in pregnant women. because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed. cefixime has not been studied for use during labor and delivery. treatment should only be given if clearly needed. it is not known whether cefixime is excreted in human milk. consideration should be given to discontinuing nursing temporarily during treatment with this drug. safety and effectiveness of cefixime in children aged less than six months old have not been established. the incidence of gastrointestinal adverse reactions, including diarrhea and loose stools, in the pediatric patients receiving the suspension, was comparable to the incidence seen in adult patients receiving tablets. clinical studies did not include sufficient numbers of subjects aged 65 and older to determine whether they respond differently than younger subjects. other reported clinical experience has not identified differences in responses between the elderly and younger patients. a pharmacokinetic study in the elderly detected differences in pharmacokinetic parameters [see clinical pharmacology ( 12.3)] . these differences were small and do not indicate a need for dosage adjustment of the drug in the elderly. the dose of cefixime should be adjusted in patients with renal impairment as well as those undergoing continuous ambulatory peritoneal dialysis (capd) and hemodialysis (hd). patients on dialysis should be monitored carefully [see dosage and administration ( 2.3)] .