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Drug overview for CEFUROXIME (cefuroxime axetil):
Generic name: cefuroxime axetil (seff-you-ROX-eem)
Drug class: Beta-Lactams
Therapeutic class: Anti-Infective Agents
Cefuroxime is a semisynthetic, second generation cephalosporin antibiotic.
Cefuroxime axetil is used orally for the treatment of mild to moderate respiratory tract infections (i.e., acute maxillary sinusitis, acute exacerbations of chronic bronchitis, secondary infections of acute bronchitis, community-acquired pneumonia+) caused by susceptible bacteria; acute bacterial otitis media; pharyngitis and tonsillitis caused by Streptococcus pyogenes (group A beta-hemolytic streptococci); mild to moderate uncomplicated skin and skin structure infections caused by Staphylococcus aureus (including beta-lactamase-producing strains) or S. pyogenes; and uncomplicated urinary tract infections caused by Escherichia coli or Klebsiella pneumoniae. Cefuroxime axetil also is used orally for the treatment of Lyme disease and has been used for the treatment of uncomplicated gonorrhea.
The manufacturers of cefuroxime axetil oral suspension state that safety and efficacy of the suspension have been established only for the treatment of pharyngitis and tonsillitis, acute otitis media, and impetigo caused by susceptible bacteria. and for the treatment of Lyme disease. Cefuroxime sodium is used parenterally in the treatment of lower respiratory tract infections (including pneumonia), serious skin and skin structure infections, genitourinary tract infections, bone and joint infections, septicemia, and meningitis caused by susceptible organisms.
Cefuroxime sodium also has been used parenterally for perioperative prophylaxis. Because cefuroxime, like other second generation cephalosporins, generally is less active against susceptible gram-positive cocci than are first generation cephalosporins, most clinicians state that cefuroxime probably should not be used in the treatment of infections caused by gram-positive bacteria when a penicillin or a first generation cephalosporin could be used. In addition, because cefuroxime generally is less active in vitro against Enterobacteriaceae than third generation cephalosporins, some clinicians state that a third generation drug such as cefotaxime or ceftriaxone generally is preferred if a parenteral cephalosporin is indicated in the treatment of infections known or suspected to be caused by these gram-negative bacteria.
Prior to initiation of cefuroxime therapy, appropriate specimens should be obtained for identification of the causative organism and in vitro susceptibility tests. If cefuroxime is started pending results of susceptibility tests, it should be discontinued if the causative organism is found to be resistant to the drug. In the treatment of known or suspected sepsis or the treatment of other serious infections when the causative organism is unknown, concomitant therapy with an aminoglycoside may be indicated pending results of in vitro susceptibility tests.
Generic name: cefuroxime axetil (seff-you-ROX-eem)
Drug class: Beta-Lactams
Therapeutic class: Anti-Infective Agents
Cefuroxime is a semisynthetic, second generation cephalosporin antibiotic.
Cefuroxime axetil is used orally for the treatment of mild to moderate respiratory tract infections (i.e., acute maxillary sinusitis, acute exacerbations of chronic bronchitis, secondary infections of acute bronchitis, community-acquired pneumonia+) caused by susceptible bacteria; acute bacterial otitis media; pharyngitis and tonsillitis caused by Streptococcus pyogenes (group A beta-hemolytic streptococci); mild to moderate uncomplicated skin and skin structure infections caused by Staphylococcus aureus (including beta-lactamase-producing strains) or S. pyogenes; and uncomplicated urinary tract infections caused by Escherichia coli or Klebsiella pneumoniae. Cefuroxime axetil also is used orally for the treatment of Lyme disease and has been used for the treatment of uncomplicated gonorrhea.
The manufacturers of cefuroxime axetil oral suspension state that safety and efficacy of the suspension have been established only for the treatment of pharyngitis and tonsillitis, acute otitis media, and impetigo caused by susceptible bacteria. and for the treatment of Lyme disease. Cefuroxime sodium is used parenterally in the treatment of lower respiratory tract infections (including pneumonia), serious skin and skin structure infections, genitourinary tract infections, bone and joint infections, septicemia, and meningitis caused by susceptible organisms.
Cefuroxime sodium also has been used parenterally for perioperative prophylaxis. Because cefuroxime, like other second generation cephalosporins, generally is less active against susceptible gram-positive cocci than are first generation cephalosporins, most clinicians state that cefuroxime probably should not be used in the treatment of infections caused by gram-positive bacteria when a penicillin or a first generation cephalosporin could be used. In addition, because cefuroxime generally is less active in vitro against Enterobacteriaceae than third generation cephalosporins, some clinicians state that a third generation drug such as cefotaxime or ceftriaxone generally is preferred if a parenteral cephalosporin is indicated in the treatment of infections known or suspected to be caused by these gram-negative bacteria.
Prior to initiation of cefuroxime therapy, appropriate specimens should be obtained for identification of the causative organism and in vitro susceptibility tests. If cefuroxime is started pending results of susceptibility tests, it should be discontinued if the causative organism is found to be resistant to the drug. In the treatment of known or suspected sepsis or the treatment of other serious infections when the causative organism is unknown, concomitant therapy with an aminoglycoside may be indicated pending results of in vitro susceptibility tests.
DRUG IMAGES
- CEFUROXIME AXETIL 500 MG TAB
- CEFUROXIME AXETIL 250 MG TAB
The following indications for CEFUROXIME (cefuroxime axetil) have been approved by the FDA:
Indications:
Acute bacterial maxillary sinusitis
Acute bacterial otitis media
Acute maxillary Haemophilus influenzae sinusitis
Acute maxillary Streptococcus pneumoniae sinusitis
Bacterial urinary tract infection
Chronic bronchitis with bacterial exacerbation
E. coli urinary tract infection
Haemophilus influenzae acute otitis media
Haemophilus influenzae bronchitis
Haemophilus influenzae chronic bronchitis
Haemophilus parainfluenzae bronchitis
Haemophilus parainfluenzae chronic bronchitis
Impetigo
Klebsiella urinary tract infection
Lower respiratory infection
Lyme disease
Moraxella catarrhalis acute otitis media
Pharyngitis due to Streptococcus pyogenes
Skin and skin structure infection
Skin and skin structure Streptococcus pyogenes infection
Staphylococcus aureus skin and skin structure infection
Streptococcus acute otitis media
Streptococcus pneumoniae bronchitis
Streptococcus pneumoniae chronic bronchitis
Tonsillitis due to Streptococcus pyogenes
Professional Synonyms:
Acute bacterial exacerbation of chronic bronchitis
Acute maxillary sinusitis due to diplococcus pneumoniae
Acute maxillary sinusitis due to Fraenkel's pneumococcus
Acute maxillary sinusitis due to H. flu
Acute maxillary sinusitis due to Haemophilus influenzae
Acute maxillary sinusitis due to Hemophilus influenzae
Acute maxillary sinusitis due to influenza bacillus
Acute maxillary sinusitis due to Pfeiffer's bacillus
Acute maxillary sinusitis due to pneumococcus
Acute maxillary sinusitis due to pneumonococcus
Acute maxillary sinusitis from Streptococcus pneumoniae
Acute otitis media due to H. flu
Acute otitis media due to Haemophilus influenzae
Acute otitis media due to Hemophilus influenzae
Acute otitis media due to influenza Bacillus
Acute otitis media due to Moraxella catarrhalis
Acute otitis media due to Pfeiffer's Bacillus
Acute otitis media due to Streptococcus species
Bacterial exacerbation of chronic bronchitis
Bacterial otitis media
Bronchitis due to Diplococcus pneumoniae
Bronchitis due to Fraenkel's Pneumococcus
Bronchitis due to Fraenkel-Weichselbaum Pneumococcus
Bronchitis due to H. flu
Bronchitis due to H. influenzae
Bronchitis due to Haemophilus influenzae
Bronchitis due to Haemophilus Parainfluenzae
Bronchitis due to Hemophilus influenzae
Bronchitis due to Hemophilus parainfluenzae
Bronchitis due to influenzae Bacillus
Bronchitis due to Pfeiffer's Bacillus
Bronchitis due to Pneumococcus
Bronchitis due to Pneumonococcus
Bronchitis due to Streptococcus pneumoniae
Chronic bronchitis due to Diplococcus pneumoniae
Chronic bronchitis due to Fraenkel's Pneumococcus
Chronic bronchitis due to H. flu
Chronic bronchitis due to H. influenzae
Chronic bronchitis due to Haemophilus influenzae
Chronic bronchitis due to Haemophilus parainfluenzae
Chronic bronchitis due to Hemophilus influenzae
Chronic bronchitis due to Hemophilus parainfluenzae
Chronic bronchitis due to influenza Bacillus
Chronic bronchitis due to Pfeiffer's Bacillus
Chronic bronchitis due to Pneumococcus
Chronic bronchitis due to Pneumonococcus
Chronic bronchitis due to Streptococcus pneumoniae
E. coli UTI
Epidemic sore throat
Fraenkel-Weichselbaum pneumococcal chronic bronchitis
Impetigo contagiosa
Impetigo vulgaris
Infection of skin and/or subcutaneous tissue
Klebsiella UTI
Lower respiratory tract infection
Pharyngitis due to group A beta-hemolytic streptococci
Pharyngitis due to Streptococcus epidemicus
Septic sore throat
Skin & skin soft tissue Streptococcus pyogenes infection
Skin and skin soft tissue Staphylococcus aureus infection
Skin and soft tissue skin infection
Streptococcal pharyngitis
Streptococcus pyogenes tonsillitis
Urinary tract infection due to Escherichia coli
Urinary tract infection due to Klebsiella species
Indications:
Acute bacterial maxillary sinusitis
Acute bacterial otitis media
Acute maxillary Haemophilus influenzae sinusitis
Acute maxillary Streptococcus pneumoniae sinusitis
Bacterial urinary tract infection
Chronic bronchitis with bacterial exacerbation
E. coli urinary tract infection
Haemophilus influenzae acute otitis media
Haemophilus influenzae bronchitis
Haemophilus influenzae chronic bronchitis
Haemophilus parainfluenzae bronchitis
Haemophilus parainfluenzae chronic bronchitis
Impetigo
Klebsiella urinary tract infection
Lower respiratory infection
Lyme disease
Moraxella catarrhalis acute otitis media
Pharyngitis due to Streptococcus pyogenes
Skin and skin structure infection
Skin and skin structure Streptococcus pyogenes infection
Staphylococcus aureus skin and skin structure infection
Streptococcus acute otitis media
Streptococcus pneumoniae bronchitis
Streptococcus pneumoniae chronic bronchitis
Tonsillitis due to Streptococcus pyogenes
Professional Synonyms:
Acute bacterial exacerbation of chronic bronchitis
Acute maxillary sinusitis due to diplococcus pneumoniae
Acute maxillary sinusitis due to Fraenkel's pneumococcus
Acute maxillary sinusitis due to H. flu
Acute maxillary sinusitis due to Haemophilus influenzae
Acute maxillary sinusitis due to Hemophilus influenzae
Acute maxillary sinusitis due to influenza bacillus
Acute maxillary sinusitis due to Pfeiffer's bacillus
Acute maxillary sinusitis due to pneumococcus
Acute maxillary sinusitis due to pneumonococcus
Acute maxillary sinusitis from Streptococcus pneumoniae
Acute otitis media due to H. flu
Acute otitis media due to Haemophilus influenzae
Acute otitis media due to Hemophilus influenzae
Acute otitis media due to influenza Bacillus
Acute otitis media due to Moraxella catarrhalis
Acute otitis media due to Pfeiffer's Bacillus
Acute otitis media due to Streptococcus species
Bacterial exacerbation of chronic bronchitis
Bacterial otitis media
Bronchitis due to Diplococcus pneumoniae
Bronchitis due to Fraenkel's Pneumococcus
Bronchitis due to Fraenkel-Weichselbaum Pneumococcus
Bronchitis due to H. flu
Bronchitis due to H. influenzae
Bronchitis due to Haemophilus influenzae
Bronchitis due to Haemophilus Parainfluenzae
Bronchitis due to Hemophilus influenzae
Bronchitis due to Hemophilus parainfluenzae
Bronchitis due to influenzae Bacillus
Bronchitis due to Pfeiffer's Bacillus
Bronchitis due to Pneumococcus
Bronchitis due to Pneumonococcus
Bronchitis due to Streptococcus pneumoniae
Chronic bronchitis due to Diplococcus pneumoniae
Chronic bronchitis due to Fraenkel's Pneumococcus
Chronic bronchitis due to H. flu
Chronic bronchitis due to H. influenzae
Chronic bronchitis due to Haemophilus influenzae
Chronic bronchitis due to Haemophilus parainfluenzae
Chronic bronchitis due to Hemophilus influenzae
Chronic bronchitis due to Hemophilus parainfluenzae
Chronic bronchitis due to influenza Bacillus
Chronic bronchitis due to Pfeiffer's Bacillus
Chronic bronchitis due to Pneumococcus
Chronic bronchitis due to Pneumonococcus
Chronic bronchitis due to Streptococcus pneumoniae
E. coli UTI
Epidemic sore throat
Fraenkel-Weichselbaum pneumococcal chronic bronchitis
Impetigo contagiosa
Impetigo vulgaris
Infection of skin and/or subcutaneous tissue
Klebsiella UTI
Lower respiratory tract infection
Pharyngitis due to group A beta-hemolytic streptococci
Pharyngitis due to Streptococcus epidemicus
Septic sore throat
Skin & skin soft tissue Streptococcus pyogenes infection
Skin and skin soft tissue Staphylococcus aureus infection
Skin and soft tissue skin infection
Streptococcal pharyngitis
Streptococcus pyogenes tonsillitis
Urinary tract infection due to Escherichia coli
Urinary tract infection due to Klebsiella species
The following dosing information is available for CEFUROXIME (cefuroxime axetil):
Dosage of cefuroxime axetil is expressed in terms of cefuroxime. Cefuroxime axetil tablets and oral suspension are not bioequivalent and are not substitutable on a mg/mg basis. (See Pharmacokinetics: Absorption.)
Dosage of cefuroxime sodium also is expressed in terms of cefuroxime and is identical for IM or IV administration.
For the treatment of uncomplicated skin and skin-structure infections in adults and adolescents 13 years of age or older, the usual oral dosage of cefuroxime given as cefuroxime axetil tablets is 250 or 500 mg twice daily for 10 days. For the treatment of uncomplicated urinary tract infections (UTIs), the usual oral dosage of cefuroxime given as cefuroxime axetil tablets is 125 or 250 mg twice daily for 7-10 days.
The usual parenteral adult dosage of cefuroxime given as cefuroxime sodium is 750 mg to 1.5 g every 8 hours. Uncomplicated UTIs, skin and skin structure infections, and uncomplicated pneumonia in adults generally respond to a parenteral dosage of 750 mg every 8 hours.
Severe or complicated infections or bone and joint infections in adults generally require 1.5 g every 8 hours and life-threatening infections or infections caused by less susceptible organisms may require 1.5 g every 6 hours.
Dosage of parenteral cefuroxime for the treatment of bacterial meningitis in adults should not exceed 3 g every 8 hours.
Cefuroxime axetil film-coated tablets and oral suspension are not bioequivalent and are not substitutable on a mg/mg basis. (See Pharmacokinetics: Absorption.)
For the treatment of most susceptible infections (except bone and joint infections or meningitis) in children 3 months of age or older, the manufacturers recommend a cefuroxime dosage of 50-100 mg/kg daily given IM or IV in equally divided doses every 6-8 hours; the manufacturer states that 100 mg/kg should be given IM or IV for more severe infections. The IM or IV dosage of cefuroxime recommended by the manufacturers for the treatment of bone and joint infections in children 3 months of age or older is 150 mg/kg daily in 3 divided doses every 8 hours.
The American Academy of Pediatrics (AAP) recommends that neonates 7 days of age or younger receive IM or IV cefuroxime in a dosage of 50 mg/kg every 12 hours, regardless of weight. Neonates 8-28 days of age should receive a dosage of 50 mg/kg every 8-12 hours if they weigh 2 kg or less or 50 mg/kg every 8 hours if they weigh more than 2 kg.
For pediatric patients beyond the neonatal period, the AAP recommends an IM or IV cefuroxime dosage of 75-100 mg/kg daily given in 3 equally divided doses for the treatment of mild to moderate infections or 100-200 mg/kg daily in 3 or 4 equally divided doses for the treatment of severe infections. These clinicians recommend that children beyond the neonatal period receive oral cefuroxime in a dosage of 20-30 mg/kg daily in 2 equally divided doses for the treatment of mild to moderate infections. The AAP states that oral cefuroxime is inappropriate for the treatment of severe infections.
Modification of usual dosage of parenteral cefuroxime is unnecessary in patients with creatinine clearances greater than 20 mL/minute. However, in patients with creatinine clearances of 20 mL/minute or less, doses and/or frequency of administration of parenteral cefuroxime must be modified in response to the degree of renal impairment, severity of the infection, and susceptibility of the causative organism. The manufacturers and some clinicians recommend that adults with creatinine clearances of 10-20 mL/minute receive 750 mg IM or IV every 12 hours and that adults with creatinine clearances less than 10 mL/minute receive 750 mg IM or IV every 24 hours.
In children with impaired renal function, the manufacturers recommend that the frequency of administration of parenteral cefuroxime be modified based on the recommendations for adults with impaired renal function.
In patients undergoing hemodialysis, a supplemental dose of parenteral cefuroxime should be given after each dialysis period.
Safety and efficacy of oral cefuroxime axetil in patients with renal impairment have not been established.
Dosage of cefuroxime sodium also is expressed in terms of cefuroxime and is identical for IM or IV administration.
For the treatment of uncomplicated skin and skin-structure infections in adults and adolescents 13 years of age or older, the usual oral dosage of cefuroxime given as cefuroxime axetil tablets is 250 or 500 mg twice daily for 10 days. For the treatment of uncomplicated urinary tract infections (UTIs), the usual oral dosage of cefuroxime given as cefuroxime axetil tablets is 125 or 250 mg twice daily for 7-10 days.
The usual parenteral adult dosage of cefuroxime given as cefuroxime sodium is 750 mg to 1.5 g every 8 hours. Uncomplicated UTIs, skin and skin structure infections, and uncomplicated pneumonia in adults generally respond to a parenteral dosage of 750 mg every 8 hours.
Severe or complicated infections or bone and joint infections in adults generally require 1.5 g every 8 hours and life-threatening infections or infections caused by less susceptible organisms may require 1.5 g every 6 hours.
Dosage of parenteral cefuroxime for the treatment of bacterial meningitis in adults should not exceed 3 g every 8 hours.
Cefuroxime axetil film-coated tablets and oral suspension are not bioequivalent and are not substitutable on a mg/mg basis. (See Pharmacokinetics: Absorption.)
For the treatment of most susceptible infections (except bone and joint infections or meningitis) in children 3 months of age or older, the manufacturers recommend a cefuroxime dosage of 50-100 mg/kg daily given IM or IV in equally divided doses every 6-8 hours; the manufacturer states that 100 mg/kg should be given IM or IV for more severe infections. The IM or IV dosage of cefuroxime recommended by the manufacturers for the treatment of bone and joint infections in children 3 months of age or older is 150 mg/kg daily in 3 divided doses every 8 hours.
The American Academy of Pediatrics (AAP) recommends that neonates 7 days of age or younger receive IM or IV cefuroxime in a dosage of 50 mg/kg every 12 hours, regardless of weight. Neonates 8-28 days of age should receive a dosage of 50 mg/kg every 8-12 hours if they weigh 2 kg or less or 50 mg/kg every 8 hours if they weigh more than 2 kg.
For pediatric patients beyond the neonatal period, the AAP recommends an IM or IV cefuroxime dosage of 75-100 mg/kg daily given in 3 equally divided doses for the treatment of mild to moderate infections or 100-200 mg/kg daily in 3 or 4 equally divided doses for the treatment of severe infections. These clinicians recommend that children beyond the neonatal period receive oral cefuroxime in a dosage of 20-30 mg/kg daily in 2 equally divided doses for the treatment of mild to moderate infections. The AAP states that oral cefuroxime is inappropriate for the treatment of severe infections.
Modification of usual dosage of parenteral cefuroxime is unnecessary in patients with creatinine clearances greater than 20 mL/minute. However, in patients with creatinine clearances of 20 mL/minute or less, doses and/or frequency of administration of parenteral cefuroxime must be modified in response to the degree of renal impairment, severity of the infection, and susceptibility of the causative organism. The manufacturers and some clinicians recommend that adults with creatinine clearances of 10-20 mL/minute receive 750 mg IM or IV every 12 hours and that adults with creatinine clearances less than 10 mL/minute receive 750 mg IM or IV every 24 hours.
In children with impaired renal function, the manufacturers recommend that the frequency of administration of parenteral cefuroxime be modified based on the recommendations for adults with impaired renal function.
In patients undergoing hemodialysis, a supplemental dose of parenteral cefuroxime should be given after each dialysis period.
Safety and efficacy of oral cefuroxime axetil in patients with renal impairment have not been established.
No enhanced Administration information available for this drug.
DRUG LABEL | DOSING TYPE | DOSING INSTRUCTIONS |
---|---|---|
CEFUROXIME AXETIL 250 MG TAB | Maintenance | Adults take 1 tablet (250 mg) by oral route every 12 hours |
CEFUROXIME AXETIL 500 MG TAB | Maintenance | Adults take 1 tablet (500 mg) by oral route every 12 hours |
DRUG LABEL | DOSING TYPE | DOSING INSTRUCTIONS |
---|---|---|
CEFUROXIME AXETIL 250 MG TAB | Maintenance | Adults take 1 tablet (250 mg) by oral route every 12 hours |
CEFUROXIME AXETIL 500 MG TAB | Maintenance | Adults take 1 tablet (500 mg) by oral route every 12 hours |
The following drug interaction information is available for CEFUROXIME (cefuroxime axetil):
There are 1 contraindications.
These drug combinations generally should not be dispensed or administered to the same patient. A manufacturer label warning that indicates the contraindication warrants inclusion of a drug combination in this category, regardless of clinical evidence or lack of clinical evidence to support the contraindication.
Drug Interaction | Drug Names |
---|---|
Live Typhoid Vaccine/Antimicrobials SEVERITY LEVEL: 1-Contraindicated Drug Combination: This drug combination is contraindicated and generally should not be dispensed or administered to the same patient. MECHANISM OF ACTION: The antimicrobial may be active against the organism in the live-vaccine. Antimicrobial therapy may prevent the vaccine organism from replicating enough to trigger an immune response.(1) CLINICAL EFFECTS: Vaccination may be ineffective. PREDISPOSING FACTORS: None determined. PATIENT MANAGEMENT: Do not give oral typhoid vaccine until 72 hours after the last dose of antimicrobial. If possible, to optimize vaccine effectiveness, do not start antibacterial drugs for 72 hours after the last dose of oral typhoid vaccine. A longer interval should be considered for long-acting antimicrobials, such as azithromycin.(3) DISCUSSION: Because antimicrobial therapy may prevent sufficient vaccine-organism replication to generate an immune response, the manufacturer of live-attenuated typhoid vaccine and the Centers for Disease Control (CDC) state that the vaccine should not be administered to patients receiving antimicrobial therapy.(1-3) |
VIVOTIF |
There are 2 severe interactions.
These drug interactions can produce serious consequences in most patients. Actions required for severe interactions include, but are not limited to, discontinuing one or both agents, adjusting dosage, altering administration scheduling, and providing additional patient monitoring. Review the full interaction monograph for more information.
Drug Interaction | Drug Names |
---|---|
Selected Cephalosporins/Long Acting Antacids; H2s;PPIs SEVERITY LEVEL: 2-Severe Interaction: Action is required to reduce the risk of severe adverse interaction. MECHANISM OF ACTION: Absorption of oral cefpodoxime or cefuroxime may be reduced in patients receiving concomitant treatment with acid reducing agents.(1-5) CLINICAL EFFECTS: Antibiotic efficacy against organisms with a high minimum inhibitory concentration (MIC) to cefpodoxime or cefuroxime could be decreased. PREDISPOSING FACTORS: Taking cefpodoxime or cefuroxime on an empty stomach magnifies this effect. PATIENT MANAGEMENT: If possible, avoid the use of H2 antagonists and proton pump inhibitors(PPIs) in patients taking cefpodoxime or cefuroxime. If concurrent therapy is needed with antacids, H2 antagonists, or PPIs, administer cefpodoxime or cefuroxime after eating to maximize oral absorption. Some vitamin preparations may contain sufficient quantities of calcium and/or magnesium salts with antacid properties to interact as well. DISCUSSION: In a study of ten subjects, administration of cefpodoxime after single dose famotidine 40 mg decreased both maximum concentration (Cmax) and area-under-curve (AUC) by approximately 40 percent compared with administration of cefpodoxime on an empty stomach.(3) In a study of 17 subjects, administration of cefpodoxime after single dose ranitidine 150 mg decreased Cmax and AUC by approximately 40 percent compared with administration of cefpodoxime on an empty stomach.(4) In a study performed prior to the introduction of PPIs, administration of ranitidine 300 mg and sodium bicarbonate followed by cefuroxime taken on a empty stomach lowered both Cmax and AUC of cefuroxime by approximately 40 per cent compared with administration of cefuroxime alone on an empty stomach. Postprandial administration of cefuroxime in subjects taking ranitidine was similar to that of subjects taking cefuroxime on an empty stomach.(5) |
ACIPHEX, ACIPHEX SPRINKLE, CIMETIDINE, DEXILANT, DEXLANSOPRAZOLE DR, ESOMEPRAZOLE MAGNESIUM, ESOMEPRAZOLE SODIUM, FAMOTIDINE, IBUPROFEN-FAMOTIDINE, KONVOMEP, LANSOPRAZOL-AMOXICIL-CLARITHRO, LANSOPRAZOLE, NAPROXEN-ESOMEPRAZOLE MAG, NEXIUM, NIZATIDINE, OMECLAMOX-PAK, OMEPRAZOLE, OMEPRAZOLE-SODIUM BICARBONATE, PANTOPRAZOLE SODIUM, PANTOPRAZOLE SODIUM-0.9% NACL, PEPCID, PREVACID, PRILOSEC, PROTONIX, PROTONIX IV, RABEPRAZOLE SODIUM, TALICIA, VIMOVO, VOQUEZNA, VOQUEZNA DUAL PAK, VOQUEZNA TRIPLE PAK, YOSPRALA |
Fecal Microbiota Spores/Antibiotics SEVERITY LEVEL: 2-Severe Interaction: Action is required to reduce the risk of severe adverse interaction. MECHANISM OF ACTION: Fecal microbiota spores is a suspension of live bacterial spores, which may be compromised by concurrent use of antibiotics.(1) CLINICAL EFFECTS: Antibiotics may decrease the effectiveness of fecal microbiota spores.(1) PREDISPOSING FACTORS: None determined. PATIENT MANAGEMENT: Antibiotics should not be used concurrently with fecal microbiota spores. Antibacterial treatment should be completed for 2 to 4 days before initiating treatment with fecal microbiota spores.(1) DISCUSSION: Antibiotics may compromise the effectiveness of fecal microbiota spores. |
VOWST |
There are 2 moderate interactions.
The clinician should assess the patient’s characteristics and take action as needed. Actions required for moderate interactions include, but are not limited to, discontinuing one or both agents, adjusting dosage, altering administration.
Drug Interaction | Drug Names |
---|---|
Selected Cephalosporins & Penicillins/Probenecid SEVERITY LEVEL: 3-Moderate Interaction: Assess the risk to the patient and take action as needed. MECHANISM OF ACTION: Probenecid impairs the clearance of some cephalosporins and penicillins via inhibition of renal anion transporters in the proximal tubule.(49) It has also been hypothesized that probenecid may affect tissue distribution of cephalosporins.(1-5) CLINICAL EFFECTS: The concurrent administration of probenecid may result in increased maximum concentration (Cmax), area-under-curve (AUC), and half-life of the cephalosporin or penicillin.(49) While this may improve antibiotic efficacy,(46-48) increased levels may also increase the risk for antibiotic-associated nephrotoxicity.(4) PREDISPOSING FACTORS: Underlying renal dysfunction may increase the risk for nephrotoxicity. PATIENT MANAGEMENT: In patients receiving the combination to improve antibiotic efficacy, monitor for antibiotic adverse effects and consider monitoring renal function. In patients receiving probenecid therapy to prevent or treat hyperuricemia, exposure to the antibiotic will be increased. A decrease in antibiotic dose or frequency may be required. The US manufacturer of piperacillin-tazobactam states probenecid should not be coadministered with piperacillin-tazobactam unless the benefit outweighs the risk.(50) DISCUSSION: Concurrent use of probenecid with a cephalosporin or penicillin may cause an increase in the Cmax, AUC, and an increased elimination half life of the antibiotic.(6-8,49) This may be beneficial or necessary in difficult to treat infections,(46-48) but an increased risk for adverse effects should be expected. Antibiotics not dose adjusted for concurrent use with probenecid may be associated with an increased risk for adverse effects, such as nephrotoxicity. Probenecid administered concurrently with piperacillin-tazobactam prolongs the half-life of piperacillin by 21% and tazobactam by 71%. In a study in 8 healthy males, concurrent administration of probenecid (1 g) with piperacillin (1 g IM) increased piperacillin's Cmax and AUC by 30% and 60%. Renal clearance was reduced by 40%.(51) The cephalosporins affected by probenecid include cefazolin,(9-11) cephacetrile,(12,13) cephaloglycin,(14,15) cephalexin,(16-21) cephradine, (22-23) cefoxitin,(24-28) cefadroxil(29), cefaclor,(23) cefamandole,(30) ceftizoxime,(31,32) cefuroxime,(33,34) cefprozil,(35) cefonicid,(36) cefmetazole,(37) cefmenoxime,(38) and cefditoren.(39) Probenecid has been shown not to affect moxalactam,(4,40,41) ceforanide, (4,42), cefoperazone, ceftazidime(4,34,43) or ceftriaxone.(4) |
PROBENECID, PROBENECID-COLCHICINE |
Selected Cephalosporins/Antacids SEVERITY LEVEL: 3-Moderate Interaction: Assess the risk to the patient and take action as needed. MECHANISM OF ACTION: Absorption of oral cefuroxime may be reduced in patients receiving concomitant treatment with acid reducing agents.(1,2) CLINICAL EFFECTS: Antibiotic efficacy against organisms with a high minimum inhibitory concentration (MIC) to cefuroxime could be decreased. PREDISPOSING FACTORS: Taking cefuroxime on an empty stomach magnifies this effect. PATIENT MANAGEMENT: Separate the administration of cefuroxime by at least 1-2 hours after administration of antacids. Some vitamin preparations may contain sufficient quantities of calcium and/or magnesium salts with antacid properties to interact as well. Since concurrent use of H2 antagonists and proton pump inhibitors (PPIs) in patients taking cefuroxime should be avoided, these would not be alternatives to antacids in these patients. DISCUSSION: In a study performed prior to the introduction of PPIs, administration of ranitidine 300 mg and sodium bicarbonate followed by cefuroxime taken on a empty stomach lowered both Cmax and AUC of cefuroxime by approximately 40 per cent compared with administration of cefuroxime alone on an empty stomach. Postprandial administration of cefuroxime in subjects taking ranitidine was similar to that of subjects taking cefuroxime on an empty stomach.(2) |
CALCIUM ACETATE, CALCIUM GLUCONATE MONOHYDRATE, GAVILYTE-C, GAVILYTE-G, GAVILYTE-N, GOLYTELY, KONVOMEP, OMEPRAZOLE-SODIUM BICARBONATE, PEG 3350-ELECTROLYTE, PEG-3350 AND ELECTROLYTES, SODIUM BICARBONATE, VAXCHORA BUFFER COMPONENT |
The following contraindication information is available for CEFUROXIME (cefuroxime axetil):
Drug contraindication overview.
No enhanced Contraindications information available for this drug.
No enhanced Contraindications information available for this drug.
There are 0 contraindications.
There are 3 severe contraindications.
Adequate patient monitoring is recommended for safer drug use.
Severe List |
---|
Chronic kidney disease stage 4 (severe) GFR 15-29 ml/min |
Chronic kidney disease stage 5 (failure) GFr<15 ml/min |
Clostridioides difficile infection |
There are 1 moderate contraindications.
Clinically significant contraindication, where the condition can be managed or treated before the drug may be given safely.
Moderate List |
---|
Hypoprothrombinemia |
The following adverse reaction information is available for CEFUROXIME (cefuroxime axetil):
Adverse reaction overview.
No enhanced Common Adverse Effects information available for this drug.
No enhanced Common Adverse Effects information available for this drug.
There are 37 severe adverse reactions.
More Frequent | Less Frequent |
---|---|
Clostridioides difficile infection Eosinophilia Hypersensitivity drug reaction Urticaria |
Kounis syndrome Skin rash |
Rare/Very Rare |
---|
Abnormal hepatic function tests Acute generalized exanthematous pustulosis Agranulocytosis Anaphylaxis Angioedema Aplastic anemia Cholestasis Cholestatic hepatitis Colitis Cutaneous vasculitis DRESS syndrome Drug-induced hepatitis Encephalopathy Erythema Erythema multiforme Hemolytic anemia Hemorrhage Hypoprothrombinemia Interstitial nephritis Kidney disease with reduction in glomerular filtration rate (GFr) Leukopenia Myocardial ischemia Neutropenic disorder Pancytopenia Seizure disorder Serum sickness Stevens-johnson syndrome Thrombocytopenic disorder Thrombophlebitis Tongue swelling Toxic epidermal necrolysis |
There are 29 less severe adverse reactions.
More Frequent | Less Frequent |
---|---|
Acute abdominal pain Diarrhea Vulvovaginal candidiasis |
Arthralgia Flatulence Irritability Nausea Oral candidiasis Pruritus of skin Sialorrhea Vaginal irritation Vomiting |
Rare/Very Rare |
---|
Abdominal pain with cramps Anorexia Aphthous stomatitis Candidiasis Chills Cramps Dizziness Drowsy Drug fever Dysgeusia Dyspnea Dysuria Polydipsia Renal pain Tachycardia Trismus Vulvovaginitis |
The following precautions are available for CEFUROXIME (cefuroxime axetil):
No enhanced Pediatric Use information available for this drug.
Contraindicated
Severe Precaution
Management or Monitoring Precaution
Contraindicated
None |
Severe Precaution
None |
Management or Monitoring Precaution
None |
Reproduction studies in mice and rabbits using cefuroxime sodium in dosages up to 6 and 2 times the usual human dosage based on mg/m2, respectively, and reproduction studies in mice and rats using cefuroxime axetil in dosages up to 14 and 9 times, respectively, the usual human dosage based on mg/m2 have not revealed evidence of impaired fertility or harm to the fetus. There are no adequate and controlled studies to date using cefuroxime in pregnant women, and cefuroxime axetil and cefuroxime sodium should be used during pregnancy only when clearly needed. Cefuroxime axetil has not been studied for use during labor and delivery.
Because cefuroxime is distributed into milk, cefuroxime axetil and cefuroxime sodium should be used with caution in nursing women.
No enhanced Geriatric Use information available for this drug.
The following prioritized warning is available for CEFUROXIME (cefuroxime axetil):
No warning message for this drug.
No warning message for this drug.
The following icd codes are available for CEFUROXIME (cefuroxime axetil)'s list of indications:
Acute bacterial maxillary sinusitis | |
J01.0 | Acute maxillary sinusitis |
J01.00 | Acute maxillary sinusitis, unspecified |
J01.01 | Acute recurrent maxillary sinusitis |
Acute bacterial otitis media | |
H66 | Suppurative and unspecified otitis media |
H66.0 | Acute suppurative otitis media |
H66.00 | Acute suppurative otitis media without spontaneous rupture of ear drum |
H66.001 | Acute suppurative otitis media without spontaneous rupture of ear drum, right ear |
H66.002 | Acute suppurative otitis media without spontaneous rupture of ear drum, left ear |
H66.003 | Acute suppurative otitis media without spontaneous rupture of ear drum, bilateral |
H66.004 | Acute suppurative otitis media without spontaneous rupture of ear drum, recurrent, right ear |
H66.005 | Acute suppurative otitis media without spontaneous rupture of ear drum, recurrent, left ear |
H66.006 | Acute suppurative otitis media without spontaneous rupture of ear drum, recurrent, bilateral |
H66.007 | Acute suppurative otitis media without spontaneous rupture of ear drum, recurrent, unspecified ear |
H66.009 | Acute suppurative otitis media without spontaneous rupture of ear drum, unspecified ear |
H66.01 | Acute suppurative otitis media with spontaneous rupture of ear drum |
H66.011 | Acute suppurative otitis media with spontaneous rupture of ear drum, right ear |
H66.012 | Acute suppurative otitis media with spontaneous rupture of ear drum, left ear |
H66.013 | Acute suppurative otitis media with spontaneous rupture of ear drum, bilateral |
H66.014 | Acute suppurative otitis media with spontaneous rupture of ear drum, recurrent, right ear |
H66.015 | Acute suppurative otitis media with spontaneous rupture of ear drum, recurrent, left ear |
H66.016 | Acute suppurative otitis media with spontaneous rupture of ear drum, recurrent, bilateral |
H66.017 | Acute suppurative otitis media with spontaneous rupture of ear drum, recurrent, unspecified ear |
H66.019 | Acute suppurative otitis media with spontaneous rupture of ear drum, unspecified ear |
H66.4 | Suppurative otitis media, unspecified |
H66.40 | Suppurative otitis media, unspecified, unspecified ear |
H66.41 | Suppurative otitis media, unspecified, right ear |
H66.42 | Suppurative otitis media, unspecified, left ear |
H66.43 | Suppurative otitis media, unspecified, bilateral |
H66.9 | Otitis media, unspecified |
H66.90 | Otitis media, unspecified, unspecified ear |
H66.91 | Otitis media, unspecified, right ear |
H66.92 | Otitis media, unspecified, left ear |
H66.93 | Otitis media, unspecified, bilateral |
Acute maxillary haemophilus influenzae sinusitis | |
B96.3 | Hemophilus influenzae [h. influenzae] as the cause of diseases classified elsewhere |
J01.0 | Acute maxillary sinusitis |
J01.00 | Acute maxillary sinusitis, unspecified |
J01.01 | Acute recurrent maxillary sinusitis |
Acute maxillary streptococcus pneumoniae sinusitis | |
B95.3 | Streptococcus pneumoniae as the cause of diseases classified elsewhere |
J01.0 | Acute maxillary sinusitis |
J01.00 | Acute maxillary sinusitis, unspecified |
J01.01 | Acute recurrent maxillary sinusitis |
Bacterial urinary tract infection | |
N30.0 | Acute cystitis |
N30.00 | Acute cystitis without hematuria |
N30.01 | Acute cystitis with hematuria |
N30.9 | Cystitis, unspecified |
N30.90 | Cystitis, unspecified without hematuria |
N30.91 | Cystitis, unspecified with hematuria |
N39.0 | Urinary tract infection, site not specified |
O23.0 | Infections of kidney in pregnancy |
O23.00 | Infections of kidney in pregnancy, unspecified trimester |
O23.01 | Infections of kidney in pregnancy, first trimester |
O23.02 | Infections of kidney in pregnancy, second trimester |
O23.03 | Infections of kidney in pregnancy, third trimester |
O23.1 | Infections of bladder in pregnancy |
O23.10 | Infections of bladder in pregnancy, unspecified trimester |
O23.11 | Infections of bladder in pregnancy, first trimester |
O23.12 | Infections of bladder in pregnancy, second trimester |
O23.13 | Infections of bladder in pregnancy, third trimester |
O23.2 | Infections of urethra in pregnancy |
O23.20 | Infections of urethra in pregnancy, unspecified trimester |
O23.21 | Infections of urethra in pregnancy, first trimester |
O23.22 | Infections of urethra in pregnancy, second trimester |
O23.23 | Infections of urethra in pregnancy, third trimester |
O23.3 | Infections of other parts of urinary tract in pregnancy |
O23.30 | Infections of other parts of urinary tract in pregnancy, unspecified trimester |
O23.31 | Infections of other parts of urinary tract in pregnancy, first trimester |
O23.32 | Infections of other parts of urinary tract in pregnancy, second trimester |
O23.33 | Infections of other parts of urinary tract in pregnancy, third trimester |
O23.4 | Unspecified infection of urinary tract in pregnancy |
O23.40 | Unspecified infection of urinary tract in pregnancy, unspecified trimester |
O23.41 | Unspecified infection of urinary tract in pregnancy, first trimester |
O23.42 | Unspecified infection of urinary tract in pregnancy, second trimester |
O23.43 | Unspecified infection of urinary tract in pregnancy, third trimester |
O23.90 | Unspecified genitourinary tract infection in pregnancy, unspecified trimester |
O23.91 | Unspecified genitourinary tract infection in pregnancy, first trimester |
O23.92 | Unspecified genitourinary tract infection in pregnancy, second trimester |
O23.93 | Unspecified genitourinary tract infection in pregnancy, third trimester |
P39.3 | Neonatal urinary tract infection |
T83 | Complications of genitourinary prosthetic devices, implants and grafts |
T83.5 | Infection and inflammatory reaction due to prosthetic device, implant and graft in urinary system |
T83.51 | Infection and inflammatory reaction due to urinary catheter |
T83.59 | Infection and inflammatory reaction due to prosthetic device, implant and graft in urinary system |
T83.6 | Infection and inflammatory reaction due to prosthetic device, implant and graft in genital tract |
Chronic bronchitis with bacterial exacerbation | |
J44.0 | Chronic obstructive pulmonary disease with (acute) lower respiratory infection |
E. coli urinary tract infection | |
B96.2 | Escherichia coli [e. coli ] as the cause of diseases classified elsewhere |
B96.20 | Unspecified escherichia coli [e. coli] as the cause of diseases classified elsewhere |
B96.29 | Other escherichia coli [e. coli] as the cause of diseases classified elsewhere |
N30.0 | Acute cystitis |
N30.00 | Acute cystitis without hematuria |
N30.01 | Acute cystitis with hematuria |
N30.9 | Cystitis, unspecified |
N30.90 | Cystitis, unspecified without hematuria |
N30.91 | Cystitis, unspecified with hematuria |
N39.0 | Urinary tract infection, site not specified |
O23.0 | Infections of kidney in pregnancy |
O23.00 | Infections of kidney in pregnancy, unspecified trimester |
O23.01 | Infections of kidney in pregnancy, first trimester |
O23.02 | Infections of kidney in pregnancy, second trimester |
O23.03 | Infections of kidney in pregnancy, third trimester |
O23.1 | Infections of bladder in pregnancy |
O23.10 | Infections of bladder in pregnancy, unspecified trimester |
O23.11 | Infections of bladder in pregnancy, first trimester |
O23.12 | Infections of bladder in pregnancy, second trimester |
O23.13 | Infections of bladder in pregnancy, third trimester |
O23.2 | Infections of urethra in pregnancy |
O23.20 | Infections of urethra in pregnancy, unspecified trimester |
O23.21 | Infections of urethra in pregnancy, first trimester |
O23.22 | Infections of urethra in pregnancy, second trimester |
O23.23 | Infections of urethra in pregnancy, third trimester |
O23.3 | Infections of other parts of urinary tract in pregnancy |
O23.30 | Infections of other parts of urinary tract in pregnancy, unspecified trimester |
O23.31 | Infections of other parts of urinary tract in pregnancy, first trimester |
O23.32 | Infections of other parts of urinary tract in pregnancy, second trimester |
O23.33 | Infections of other parts of urinary tract in pregnancy, third trimester |
O23.4 | Unspecified infection of urinary tract in pregnancy |
O23.40 | Unspecified infection of urinary tract in pregnancy, unspecified trimester |
O23.41 | Unspecified infection of urinary tract in pregnancy, first trimester |
O23.42 | Unspecified infection of urinary tract in pregnancy, second trimester |
O23.43 | Unspecified infection of urinary tract in pregnancy, third trimester |
O23.9 | Unspecified genitourinary tract infection in pregnancy |
O23.90 | Unspecified genitourinary tract infection in pregnancy, unspecified trimester |
O23.91 | Unspecified genitourinary tract infection in pregnancy, first trimester |
O23.92 | Unspecified genitourinary tract infection in pregnancy, second trimester |
O23.93 | Unspecified genitourinary tract infection in pregnancy, third trimester |
Haemophilus influenzae acute otitis media | |
B96.3 | Hemophilus influenzae [h. influenzae] as the cause of diseases classified elsewhere |
H66.0 | Acute suppurative otitis media |
H66.00 | Acute suppurative otitis media without spontaneous rupture of ear drum |
H66.001 | Acute suppurative otitis media without spontaneous rupture of ear drum, right ear |
H66.002 | Acute suppurative otitis media without spontaneous rupture of ear drum, left ear |
H66.003 | Acute suppurative otitis media without spontaneous rupture of ear drum, bilateral |
H66.004 | Acute suppurative otitis media without spontaneous rupture of ear drum, recurrent, right ear |
H66.005 | Acute suppurative otitis media without spontaneous rupture of ear drum, recurrent, left ear |
H66.006 | Acute suppurative otitis media without spontaneous rupture of ear drum, recurrent, bilateral |
H66.007 | Acute suppurative otitis media without spontaneous rupture of ear drum, recurrent, unspecified ear |
H66.009 | Acute suppurative otitis media without spontaneous rupture of ear drum, unspecified ear |
H66.01 | Acute suppurative otitis media with spontaneous rupture of ear drum |
H66.011 | Acute suppurative otitis media with spontaneous rupture of ear drum, right ear |
H66.012 | Acute suppurative otitis media with spontaneous rupture of ear drum, left ear |
H66.013 | Acute suppurative otitis media with spontaneous rupture of ear drum, bilateral |
H66.014 | Acute suppurative otitis media with spontaneous rupture of ear drum, recurrent, right ear |
H66.015 | Acute suppurative otitis media with spontaneous rupture of ear drum, recurrent, left ear |
H66.016 | Acute suppurative otitis media with spontaneous rupture of ear drum, recurrent, bilateral |
H66.017 | Acute suppurative otitis media with spontaneous rupture of ear drum, recurrent, unspecified ear |
H66.019 | Acute suppurative otitis media with spontaneous rupture of ear drum, unspecified ear |
H66.9 | Otitis media, unspecified |
H66.90 | Otitis media, unspecified, unspecified ear |
H66.91 | Otitis media, unspecified, right ear |
H66.92 | Otitis media, unspecified, left ear |
H66.93 | Otitis media, unspecified, bilateral |
Haemophilus influenzae bronchitis | |
J20.1 | Acute bronchitis due to hemophilus influenzae |
Haemophilus influenzae chronic bronchitis | |
J44.0 | Chronic obstructive pulmonary disease with (acute) lower respiratory infection |
Haemophilus parainfluenzae bronchitis | |
B96.89 | Other specified bacterial agents as the cause of diseases classified elsewhere |
J20.8 | Acute bronchitis due to other specified organisms |
Haemophilus parainfluenzae chronic bronchitis | |
J44.0 | Chronic obstructive pulmonary disease with (acute) lower respiratory infection |
Impetigo | |
L01 | Impetigo |
L01.0 | Impetigo |
L01.00 | Impetigo, unspecified |
L01.03 | Bullous impetigo |
L01.09 | Other impetigo |
L01.1 | Impetiginization of other dermatoses |
Klebsiella urinary tract infection | |
B96.1 | Klebsiella pneumoniae [k. pneumoniae] as the cause of diseases classified elsewhere |
N30.0 | Acute cystitis |
N30.00 | Acute cystitis without hematuria |
N30.01 | Acute cystitis with hematuria |
N30.9 | Cystitis, unspecified |
N30.90 | Cystitis, unspecified without hematuria |
N30.91 | Cystitis, unspecified with hematuria |
N39.0 | Urinary tract infection, site not specified |
O23.0 | Infections of kidney in pregnancy |
O23.00 | Infections of kidney in pregnancy, unspecified trimester |
O23.01 | Infections of kidney in pregnancy, first trimester |
O23.02 | Infections of kidney in pregnancy, second trimester |
O23.03 | Infections of kidney in pregnancy, third trimester |
O23.1 | Infections of bladder in pregnancy |
O23.10 | Infections of bladder in pregnancy, unspecified trimester |
O23.11 | Infections of bladder in pregnancy, first trimester |
O23.12 | Infections of bladder in pregnancy, second trimester |
O23.13 | Infections of bladder in pregnancy, third trimester |
O23.2 | Infections of urethra in pregnancy |
O23.20 | Infections of urethra in pregnancy, unspecified trimester |
O23.21 | Infections of urethra in pregnancy, first trimester |
O23.22 | Infections of urethra in pregnancy, second trimester |
O23.23 | Infections of urethra in pregnancy, third trimester |
O23.3 | Infections of other parts of urinary tract in pregnancy |
O23.30 | Infections of other parts of urinary tract in pregnancy, unspecified trimester |
O23.31 | Infections of other parts of urinary tract in pregnancy, first trimester |
O23.32 | Infections of other parts of urinary tract in pregnancy, second trimester |
O23.33 | Infections of other parts of urinary tract in pregnancy, third trimester |
O23.4 | Unspecified infection of urinary tract in pregnancy |
O23.40 | Unspecified infection of urinary tract in pregnancy, unspecified trimester |
O23.41 | Unspecified infection of urinary tract in pregnancy, first trimester |
O23.42 | Unspecified infection of urinary tract in pregnancy, second trimester |
O23.43 | Unspecified infection of urinary tract in pregnancy, third trimester |
O23.9 | Unspecified genitourinary tract infection in pregnancy |
O23.90 | Unspecified genitourinary tract infection in pregnancy, unspecified trimester |
O23.91 | Unspecified genitourinary tract infection in pregnancy, first trimester |
O23.92 | Unspecified genitourinary tract infection in pregnancy, second trimester |
O23.93 | Unspecified genitourinary tract infection in pregnancy, third trimester |
Lower respiratory infection | |
J15.9 | Unspecified bacterial pneumonia |
J18.9 | Pneumonia, unspecified organism |
J22 | Unspecified acute lower respiratory infection |
Lyme disease | |
A69.20 | Lyme disease, unspecified |
Moraxella catarrhalis acute otitis media | |
B96.89 | Other specified bacterial agents as the cause of diseases classified elsewhere |
H66.0 | Acute suppurative otitis media |
H66.00 | Acute suppurative otitis media without spontaneous rupture of ear drum |
H66.001 | Acute suppurative otitis media without spontaneous rupture of ear drum, right ear |
H66.002 | Acute suppurative otitis media without spontaneous rupture of ear drum, left ear |
H66.003 | Acute suppurative otitis media without spontaneous rupture of ear drum, bilateral |
H66.004 | Acute suppurative otitis media without spontaneous rupture of ear drum, recurrent, right ear |
H66.005 | Acute suppurative otitis media without spontaneous rupture of ear drum, recurrent, left ear |
H66.006 | Acute suppurative otitis media without spontaneous rupture of ear drum, recurrent, bilateral |
H66.007 | Acute suppurative otitis media without spontaneous rupture of ear drum, recurrent, unspecified ear |
H66.009 | Acute suppurative otitis media without spontaneous rupture of ear drum, unspecified ear |
H66.01 | Acute suppurative otitis media with spontaneous rupture of ear drum |
H66.011 | Acute suppurative otitis media with spontaneous rupture of ear drum, right ear |
H66.012 | Acute suppurative otitis media with spontaneous rupture of ear drum, left ear |
H66.013 | Acute suppurative otitis media with spontaneous rupture of ear drum, bilateral |
H66.014 | Acute suppurative otitis media with spontaneous rupture of ear drum, recurrent, right ear |
H66.015 | Acute suppurative otitis media with spontaneous rupture of ear drum, recurrent, left ear |
H66.016 | Acute suppurative otitis media with spontaneous rupture of ear drum, recurrent, bilateral |
H66.017 | Acute suppurative otitis media with spontaneous rupture of ear drum, recurrent, unspecified ear |
H66.019 | Acute suppurative otitis media with spontaneous rupture of ear drum, unspecified ear |
H66.4 | Suppurative otitis media, unspecified |
H66.40 | Suppurative otitis media, unspecified, unspecified ear |
H66.41 | Suppurative otitis media, unspecified, right ear |
H66.42 | Suppurative otitis media, unspecified, left ear |
H66.43 | Suppurative otitis media, unspecified, bilateral |
H66.9 | Otitis media, unspecified |
H66.91 | Otitis media, unspecified, right ear |
H66.92 | Otitis media, unspecified, left ear |
H66.93 | Otitis media, unspecified, bilateral |
Pharyngitis due to streptococcus pyogenes | |
J02.0 | Streptococcal pharyngitis |
Skin and skin structure infection | |
H05.01 | Cellulitis of orbit |
H05.011 | Cellulitis of right orbit |
H05.012 | Cellulitis of left orbit |
H05.013 | Cellulitis of bilateral orbits |
H05.019 | Cellulitis of unspecified orbit |
H60.1 | Cellulitis of external ear |
H60.10 | Cellulitis of external ear, unspecified ear |
H60.11 | Cellulitis of right external ear |
H60.12 | Cellulitis of left external ear |
H60.13 | Cellulitis of external ear, bilateral |
K12.2 | Cellulitis and abscess of mouth |
L03 | Cellulitis and acute lymphangitis |
L03.0 | Cellulitis and acute lymphangitis of finger and toe |
L03.01 | Cellulitis of finger |
L03.011 | Cellulitis of right finger |
L03.012 | Cellulitis of left finger |
L03.019 | Cellulitis of unspecified finger |
L03.03 | Cellulitis of toe |
L03.031 | Cellulitis of right toe |
L03.032 | Cellulitis of left toe |
L03.039 | Cellulitis of unspecified toe |
L03.1 | Cellulitis and acute lymphangitis of other parts of limb |
L03.11 | Cellulitis of other parts of limb |
L03.111 | Cellulitis of right axilla |
L03.112 | Cellulitis of left axilla |
L03.113 | Cellulitis of right upper limb |
L03.114 | Cellulitis of left upper limb |
L03.115 | Cellulitis of right lower limb |
L03.116 | Cellulitis of left lower limb |
L03.119 | Cellulitis of unspecified part of limb |
L03.2 | Cellulitis and acute lymphangitis of face and neck |
L03.21 | Cellulitis and acute lymphangitis of face |
L03.211 | Cellulitis of face |
L03.22 | Cellulitis and acute lymphangitis of neck |
L03.221 | Cellulitis of neck |
L03.3 | Cellulitis and acute lymphangitis of trunk |
L03.31 | Cellulitis of trunk |
L03.311 | Cellulitis of abdominal wall |
L03.312 | Cellulitis of back [any part except buttock] |
L03.313 | Cellulitis of chest wall |
L03.314 | Cellulitis of groin |
L03.315 | Cellulitis of perineum |
L03.316 | Cellulitis of umbilicus |
L03.317 | Cellulitis of buttock |
L03.319 | Cellulitis of trunk, unspecified |
L03.8 | Cellulitis and acute lymphangitis of other sites |
L03.81 | Cellulitis of other sites |
L03.811 | Cellulitis of head [any part, except face] |
L03.818 | Cellulitis of other sites |
L03.9 | Cellulitis and acute lymphangitis, unspecified |
L03.90 | Cellulitis, unspecified |
L08.9 | Local infection of the skin and subcutaneous tissue, unspecified |
N48.22 | Cellulitis of corpus cavernosum and penis |
Skin and skin structure strep. pyogenes infection | |
B95.0 | Streptococcus, group a, as the cause of diseases classified elsewhere |
B95.4 | Other streptococcus as the cause of diseases classified elsewhere |
L08.89 | Other specified local infections of the skin and subcutaneous tissue |
L08.9 | Local infection of the skin and subcutaneous tissue, unspecified |
Staphylococcus aureus skin and skin structure infection | |
B95.6 | Staphylococcus aureus as the cause of diseases classified elsewhere |
H60.1 | Cellulitis of external ear |
H60.10 | Cellulitis of external ear, unspecified ear |
H60.11 | Cellulitis of right external ear |
H60.12 | Cellulitis of left external ear |
H60.13 | Cellulitis of external ear, bilateral |
J34.0 | Abscess, furuncle and carbuncle of nose |
L02 | Cutaneous abscess, furuncle and carbuncle |
L02.0 | Cutaneous abscess, furuncle and carbuncle of face |
L02.02 | Furuncle of face |
L02.03 | Carbuncle of face |
L02.1 | Cutaneous abscess, furuncle and carbuncle of neck |
L02.12 | Furuncle of neck |
L02.13 | Carbuncle of neck |
L02.2 | Cutaneous abscess, furuncle and carbuncle of trunk |
L02.22 | Furuncle of trunk |
L02.221 | Furuncle of abdominal wall |
L02.222 | Furuncle of back [any part, except buttock] |
L02.223 | Furuncle of chest wall |
L02.224 | Furuncle of groin |
L02.225 | Furuncle of perineum |
L02.226 | Furuncle of umbilicus |
L02.229 | Furuncle of trunk, unspecified |
L02.23 | Carbuncle of trunk |
L02.231 | Carbuncle of abdominal wall |
L02.232 | Carbuncle of back [any part, except buttock] |
L02.233 | Carbuncle of chest wall |
L02.234 | Carbuncle of groin |
L02.235 | Carbuncle of perineum |
L02.236 | Carbuncle of umbilicus |
L02.239 | Carbuncle of trunk, unspecified |
L02.3 | Cutaneous abscess, furuncle and carbuncle of buttock |
L02.32 | Furuncle of buttock |
L02.33 | Carbuncle of buttock |
L02.4 | Cutaneous abscess, furuncle and carbuncle of limb |
L02.42 | Furuncle of limb |
L02.421 | Furuncle of right axilla |
L02.422 | Furuncle of left axilla |
L02.423 | Furuncle of right upper limb |
L02.424 | Furuncle of left upper limb |
L02.425 | Furuncle of right lower limb |
L02.426 | Furuncle of left lower limb |
L02.429 | Furuncle of limb, unspecified |
L02.43 | Carbuncle of limb |
L02.431 | Carbuncle of right axilla |
L02.432 | Carbuncle of left axilla |
L02.433 | Carbuncle of right upper limb |
L02.434 | Carbuncle of left upper limb |
L02.435 | Carbuncle of right lower limb |
L02.436 | Carbuncle of left lower limb |
L02.439 | Carbuncle of limb, unspecified |
L02.5 | Cutaneous abscess, furuncle and carbuncle of hand |
L02.52 | Furuncle hand |
L02.521 | Furuncle right hand |
L02.522 | Furuncle left hand |
L02.529 | Furuncle unspecified hand |
L02.53 | Carbuncle of hand |
L02.531 | Carbuncle of right hand |
L02.532 | Carbuncle of left hand |
L02.539 | Carbuncle of unspecified hand |
L02.6 | Cutaneous abscess, furuncle and carbuncle of foot |
L02.62 | Furuncle of foot |
L02.621 | Furuncle of right foot |
L02.622 | Furuncle of left foot |
L02.629 | Furuncle of unspecified foot |
L02.63 | Carbuncle of foot |
L02.631 | Carbuncle of right foot |
L02.632 | Carbuncle of left foot |
L02.639 | Carbuncle of unspecified foot |
L02.8 | Cutaneous abscess, furuncle and carbuncle of other sites |
L02.82 | Furuncle of other sites |
L02.821 | Furuncle of head [any part, except face] |
L02.828 | Furuncle of other sites |
L02.83 | Carbuncle of other sites |
L02.831 | Carbuncle of head [any part, except face] |
L02.838 | Carbuncle of other sites |
L02.9 | Cutaneous abscess, furuncle and carbuncle, unspecified |
L02.92 | Furuncle, unspecified |
L02.93 | Carbuncle, unspecified |
L03.01 | Cellulitis of finger |
L03.011 | Cellulitis of right finger |
L03.012 | Cellulitis of left finger |
L03.019 | Cellulitis of unspecified finger |
L03.03 | Cellulitis of toe |
L03.031 | Cellulitis of right toe |
L03.032 | Cellulitis of left toe |
L03.039 | Cellulitis of unspecified toe |
L03.1 | Cellulitis and acute lymphangitis of other parts of limb |
L03.11 | Cellulitis of other parts of limb |
L03.111 | Cellulitis of right axilla |
L03.112 | Cellulitis of left axilla |
L03.113 | Cellulitis of right upper limb |
L03.114 | Cellulitis of left upper limb |
L03.115 | Cellulitis of right lower limb |
L03.116 | Cellulitis of left lower limb |
L03.119 | Cellulitis of unspecified part of limb |
L03.2 | Cellulitis and acute lymphangitis of face and neck |
L03.21 | Cellulitis and acute lymphangitis of face |
L03.211 | Cellulitis of face |
L03.22 | Cellulitis and acute lymphangitis of neck |
L03.221 | Cellulitis of neck |
L03.3 | Cellulitis and acute lymphangitis of trunk |
L03.31 | Cellulitis of trunk |
L03.311 | Cellulitis of abdominal wall |
L03.312 | Cellulitis of back [any part except buttock] |
L03.313 | Cellulitis of chest wall |
L03.314 | Cellulitis of groin |
L03.315 | Cellulitis of perineum |
L03.316 | Cellulitis of umbilicus |
L03.317 | Cellulitis of buttock |
L03.319 | Cellulitis of trunk, unspecified |
L03.8 | Cellulitis and acute lymphangitis of other sites |
L03.81 | Cellulitis of other sites |
L03.811 | Cellulitis of head [any part, except face] |
L03.818 | Cellulitis of other sites |
L03.9 | Cellulitis and acute lymphangitis, unspecified |
L03.90 | Cellulitis, unspecified |
L08.89 | Other specified local infections of the skin and subcutaneous tissue |
L08.9 | Local infection of the skin and subcutaneous tissue, unspecified |
N48.22 | Cellulitis of corpus cavernosum and penis |
Streptococcus acute otitis media | |
B95.0 | Streptococcus, group a, as the cause of diseases classified elsewhere |
B95.4 | Other streptococcus as the cause of diseases classified elsewhere |
B95.5 | Unspecified streptococcus as the cause of diseases classified elsewhere |
H66.0 | Acute suppurative otitis media |
H66.00 | Acute suppurative otitis media without spontaneous rupture of ear drum |
H66.001 | Acute suppurative otitis media without spontaneous rupture of ear drum, right ear |
H66.002 | Acute suppurative otitis media without spontaneous rupture of ear drum, left ear |
H66.003 | Acute suppurative otitis media without spontaneous rupture of ear drum, bilateral |
H66.004 | Acute suppurative otitis media without spontaneous rupture of ear drum, recurrent, right ear |
H66.005 | Acute suppurative otitis media without spontaneous rupture of ear drum, recurrent, left ear |
H66.006 | Acute suppurative otitis media without spontaneous rupture of ear drum, recurrent, bilateral |
H66.007 | Acute suppurative otitis media without spontaneous rupture of ear drum, recurrent, unspecified ear |
H66.009 | Acute suppurative otitis media without spontaneous rupture of ear drum, unspecified ear |
H66.01 | Acute suppurative otitis media with spontaneous rupture of ear drum |
H66.011 | Acute suppurative otitis media with spontaneous rupture of ear drum, right ear |
H66.012 | Acute suppurative otitis media with spontaneous rupture of ear drum, left ear |
H66.013 | Acute suppurative otitis media with spontaneous rupture of ear drum, bilateral |
H66.014 | Acute suppurative otitis media with spontaneous rupture of ear drum, recurrent, right ear |
H66.015 | Acute suppurative otitis media with spontaneous rupture of ear drum, recurrent, left ear |
H66.016 | Acute suppurative otitis media with spontaneous rupture of ear drum, recurrent, bilateral |
H66.017 | Acute suppurative otitis media with spontaneous rupture of ear drum, recurrent, unspecified ear |
H66.019 | Acute suppurative otitis media with spontaneous rupture of ear drum, unspecified ear |
H66.4 | Suppurative otitis media, unspecified |
H66.40 | Suppurative otitis media, unspecified, unspecified ear |
H66.41 | Suppurative otitis media, unspecified, right ear |
H66.42 | Suppurative otitis media, unspecified, left ear |
H66.43 | Suppurative otitis media, unspecified, bilateral |
H66.9 | Otitis media, unspecified |
H66.90 | Otitis media, unspecified, unspecified ear |
H66.91 | Otitis media, unspecified, right ear |
H66.92 | Otitis media, unspecified, left ear |
H66.93 | Otitis media, unspecified, bilateral |
Streptococcus pneumoniae bronchitis | |
B95.3 | Streptococcus pneumoniae as the cause of diseases classified elsewhere |
J20.2 | Acute bronchitis due to streptococcus |
Streptococcus pneumoniae chronic bronchitis | |
B95.3 | Streptococcus pneumoniae as the cause of diseases classified elsewhere |
J41 | Simple and mucopurulent chronic bronchitis |
J41.0 | Simple chronic bronchitis |
J41.1 | Mucopurulent chronic bronchitis |
J42 | Unspecified chronic bronchitis |
Tonsillitis due to streptococcus pyogenes | |
J03.0 | Streptococcal tonsillitis |
J03.00 | Acute streptococcal tonsillitis, unspecified |
J03.01 | Acute recurrent streptococcal tonsillitis |
Formulary Reference Tool