CEFUROXIME AXETIL tablet, film coated

Cefuroxime Axetil by

Drug Labeling and Warnings

Cefuroxime Axetil by is a Prescription medication manufactured, distributed, or labeled by NuCare Pharmaceuticals,Inc., Aurobindo Pharma Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • 1 INDICATIONS AND USAGE

    1.1 Pharyngitis/Tonsillitis

    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 tablets in the prevention of rheumatic fever was not established in clinical trials.
    • The efficacy of cefuroxime axetil tablets in the treatment of penicillin-resistant strains of Streptococcus pyogenes has not been demonstrated in clinical trials.

    1.2 Acute Bacterial Otitis Media

    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.

    1.3 Acute Bacterial Maxillary Sinusitis

    Cefuroxime axetil tablets are indicated for the treatment of adult and pediatric patients (13 years and older) with mild-to-moderate acute bacterial maxillary sinusitis caused by susceptible strains of Streptococcus pneumoniae or Haemophilus influenzae (non -β-lactamase–producing strains only).


    Limitations of Use


    The effectiveness of cefuroxime axetil tablets for sinus infections caused by β-lactamase–producing Haemophilus influenzae or Moraxella catarrhalis in patients with acute bacterial maxillary sinusitis was not established due to insufficient numbers of these isolates in the clinical trials [see Clinical Studies (14.1)] .

    1.4 Acute Bacterial Exacerbations of Chronic Bronchitis

    Cefuroxime axetil tablets are indicated for the treatment of adult patients and pediatric patients (aged 13 and older) with mild-to-moderate acute bacterial exacerbations of chronic bronchitis caused by susceptible strains of Streptococcus pneumoniae, Haemophilus influenzae (β-lactamase–negative strains), or Haemophilus parainfluenzae (β-lactamase–negative strains).

    1.5 Uncomplicated Skin and Skin-Structure Infections

    Cefuroxime axetil tablets are indicated for the treatment of adult patients and pediatric patients (aged 13 and older) with uncomplicated skin and skin-structure infections caused by susceptible strains of Staphylococcus aureus (including β -lactamase–producing strains) or Streptococcus pyogenes.

    1.6 Uncomplicated Urinary Tract Infections

    Cefuroxime axetil tablets are indicated for the treatment of adult patients and pediatric patients (aged 13 and older) with uncomplicated urinary tract infections caused by susceptible strains of Escherichia coli or Klebsiella pneumoniae.

    1.7 Uncomplicated Gonorrhea

    Cefuroxime axetil tablets are indicated for the treatment of adult patients and pediatric patients (aged 13 and older) with uncomplicated gonorrhea, urethral and endocervical, caused by penicillinase-producing and non-penicillinase–producing susceptible strains of Neisseria gonorrhoeae and uncomplicated gonorrhea, rectal, in females, caused by non-penicillinase–producing susceptible strains of Neisseria gonorrhoeae.

    1.8 Early Lyme Disease (erythema migrans)

    Cefuroxime axetil tablets are indicated for the treatment of adult patients and pediatric patients (aged 13 and older) with early Lyme disease (erythema migrans) caused by susceptible strains of Borrelia burgdorferi.

    1.10 Usage

    To reduce the development of drug-resistant bacteria and maintain the effectiveness of cefuroxime axetil tablets and other antibacterial drugs, cefuroxime axetil tablets 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.

  • 2 DOSAGE AND ADMINISTRATION

    2.1 Important Administration Instructions

    • Cefuroxime axetil tablets and cefuroxime axetil for oral suspension are not bioequivalent and are therefore not substitutable on a milligram-per-milligram basis [see Clinical Pharmacology (12.3)] .
    • Administer cefuroxime axetil tablets as described in the appropriate dosage guidelines [see Dosage and Administration (2.2)].
    • Administer cefuroxime axetil tablets with or without food.
    • Pediatric patients (aged 13 years and older) who cannot swallow the cefuroxime axetil tablets whole should receive cefuroxime axetil for oral suspension because the tablet has a strong, persistent bitter taste when crushed [see Dosage and Administration (2.2)].

    2.2 Dosage for Cefuroxime Axetil Tablets

    Administer cefuroxime axetil tablets as described in the dosage guidelines table below with or without food.

    Table 1. Adult Patients and Pediatric Patients Dosage Guidelines for Cefuroxime Axetil Tablets
    a The safety and effectiveness of cefuroxime axetil tablets  administered for less than 10 days in patients with acute exacerbations of chronic bronchitis have not been established.
    b When crushed, the tablet has a strong, persistent bitter taste. Therefore, patients who cannot swallow the tablet whole should receive the oral suspension.
     
    Infection
    		Dosage
    		Duration
    (Days)
    Adults and Adolescents (13 years and older)
    Pharyngitis/tonsillitis (mild to moderate)
    		250 mg every 12 hours
    		10
    Acute bacterial maxillary sinusitis (mild to moderate)
    		250 mg every 12 hours
    		10
    Acute bacterial exacerbations  of chronic bronchitis (mild to moderate)
    		250 mg or 500 mg every
    12 hours
    		10 a
    Uncomplicated skin and skin-structure infections
    		250 mg or 500 mg every
    12 hours
    		10
    Uncomplicated urinary tract infections
    		250 mg every 12 hours
    		7 to 10
    Uncomplicated gonorrhea
    		1,000 mg
    		single dose
    Early  Lyme disease
    		500 mg every 12 hours
    		20
    Pediatric Patients younger than 13 years (who can swallow tablets whole) b
    Acute bacterial otitis media
    		250 mg every 12 hours
    		10
    Acute bacterial maxillary sinusitis
    		250 mg every 12 hours
    		10

    2.5 Dosage in Patients with Impaired Renal Function

    A dosage interval adjustment is required for patients whose creatinine clearance is less than 30 mL/min, as listed in Table 4 below, because cefuroxime is eliminated primarily by the kidney [see Clinical Pharmacology (12.3)].

    Table 4. Dosing in Adults with Renal Impairment
    Creatinine Clearance (mL/min)
    		Recommended Dosage
    ≥30
    		No dosage adjustment
    10 to <30
    		Standard individual dose given every 24 hours
    <10 (without hemodialysis)
    		Standard individual dose given every 48 hours
    Hemodialysis
    		A single additional standard dose should be given at the end of each dialysis
  • 3 DOSAGE FORMS AND STRENGTHS

    Cefuroxime Axetil Tablets USP, 250 mg of cefuroxime (as cefuroxime axetil), are  white to off-white, film-coated, capsule shaped tablets with ‘A33’ debossed on one side and plain on the other side.

    Cefuroxime Axetil Tablets USP, 500 mg of cefuroxime (as cefuroxime axetil), are  white to off-white, film-coated, capsule shaped tablets with ‘A34’ debossed on one side and plain on the other side.

  • 4 CONTRAINDICATIONS

    Cefuroxime axetil tablets are contraindicated in patients with a known hypersensitivity (e.g., anaphylaxis) to cefuroxime axetil tablets or to other β-lactam antibacterial drugs (e.g., penicillins and cephalosporins).

  • 5 WARNINGS AND PRECAUTIONS

    5.1 Anaphylactic Reactions

    Serious and occasionally fatal hypersensitivity (anaphylactic) reactions have been reported in patients on β-lactam antibacterials, including cefuroxime axetil [see Adverse Reactions (6.2)] . These reactions are more likely to occur in individuals with a history of β-lactam hypersensitivity and/or a history of sensitivity to multiple allergens. There have been reports of individuals with a history of penicillin hypersensitivity who have experienced severe reactions when treated with cephalosporins. Cefuroxime axetil is contraindicated in patients with a known hypersensitivity to cefuroxime axetil or other β-lactam antibacterial drugs [see Contraindications (4)] . Before initiating therapy with cefuroxime axetil, inquire about previous hypersensitivity reactions to penicillins, cephalosporins, or other allergens. If an allergic reaction occurs, discontinue cefuroxime axetil and institute appropriate therapy.

    5.2  Clostridioides difficile-Associated Diarrhea

    Clostridioides difficile- associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents, including cefuroxime axetil, and may range in severity from mild diarrhea to fatal colitis. Treatment with antibacterial agents alters the normal flora of the colon leading to overgrowth of C. difficile.

    C. difficile     produces toxins A and B which contribute to the development of CDAD. Hypertoxin-producing strains of C. difficile cause increased morbidity and mortality, as these infections can be refractory to antimicrobial therapy and may require colectomy. CDAD must be considered in all patients who present with diarrhea following antibiotic use. Careful medical history is necessary since CDAD has been reported to occur over 2 months after the administration of antibacterial agents.

    If CDAD is suspected or confirmed, ongoing antibiotic use not directed against C. difficile may need to be discontinued. Appropriate fluid and electrolyte management, protein supplementation, antibiotic treatment of C. difficile, and surgical evaluation should be instituted as clinically indicated.

    5.3 Potential for Microbial Overgrowth

    The possibility of superinfections with fungal or bacterial pathogens should be considered during therapy.

    5.4 Development of Drug-Resistant Bacteria

    Prescribing cefuroxime axetil either in the absence of a proven or strongly suspected bacterial infection or a prophylactic indication is unlikely to provide benefit to the patient and increases the risk of the development of drug-resistant bacteria.

    5.6 Interference with Glucose Tests

    A false-positive result for glucose in the urine may occur with copper reduction tests, and a false-negative result for blood/plasma glucose may occur with ferricyanide tests in subjects receiving cefuroxime axetil [see Drug Interactions (7.3)] .

  • 6 ADVERSE REACTIONS

    The following serious and otherwise important adverse reaction is described in greater detail in the Warnings and Precautions section of the label:


    Anaphylactic Reactions [see Warnings and Precautions (5.1)].

    6.1 Clinical Trials Experience

    Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared with rates in the clinical trials of another drug and may not reflect the rates observed in practice.


    Tablets


    Multiple-Dose Dosing Regimens with 7 to 10 Days’ Duration: In multiple-dose clinical trials, 912 subjects were treated with cefuroxime axetil (125 to 500 mg twice daily). It is noted that 125 mg twice daily is not an approved dosage. Twenty (2.2%) subjects discontinued medication due to adverse reactions. Seventeen (85%) of the 20 subjects who discontinued therapy did so because of gastrointestinal disturbances, including diarrhea, nausea, vomiting, and abdominal pain. The percentage of subjects treated with cefuroxime axetil who discontinued study drug because of adverse reactions was similar at daily doses of 1,000, 500, and 250 mg (2.3%, 2.1%, and 2.2%, respectively). However, the incidence of gastrointestinal adverse reactions increased with the higher recommended doses.


    The adverse reactions in Table 5 are for subjects (n = 912) treated with cefuroxime axetil in multiple-dose clinical trials.


    Table 5. Adverse Reactions (≥1%) after Multiple-Dose Regimens with Cefuroxime Axetil Tablets
    Adverse Reaction
    		Cefuroxime Axetil
    (n = 912)
    Blood and lymphatic system disorders
    		 
      Eosinophilia
    		1%
    Gastrointestinal disorders
    		 
      Diarrhea
    		4%
      Nausea/Vomiting
    		3%
    Investigations
    		 
      Transient elevation in AST
    		2%
      Transient elevation in ALT
    		2%
      Transient elevation in LDH
    		1%

    The following adverse reactions occurred in less than 1% but greater than 0.1% of subjects   (n = 912) treated with cefuroxime axetil in multiple-dose clinical trials.

        Immune System Disorders:     Hives, swollen tongue.

        Metabolism and Nutrition Disorders: Anorexia.

        Nervous System Disorders: Headache.

        Cardiac Disorders:     Chest pain.

        Respiratory Disorders:     Shortness of breath.

        Gastrointestinal Disorders:     Abdominal pain, abdominal cramps, flatulence, indigestion, mouth ulcers.

        Skin and Subcutaneous Tissue Disorders:     Rash, itch.

        Renal and Urinary Disorders:     Dysuria.

        Reproductive System and Breast Disorders:     Vaginitis, vulvar itch.

        General Disorders and Administration Site Conditions:     Chills, sleepiness, thirst.

        Investigations:     Positive Coombs’ test.

    Early Lyme Disease with 20-Day Regimen:     Two multicenter trials assessed cefuroxime axetil 500 mg twice daily for 20 days. The most common drug-related adverse experiences were diarrhea (10.6%), Jarisch-Herxheimer reaction (5.6%), and vaginitis (5.4%). Other adverse experiences occurred with frequencies comparable to those reported with 7 to 10 days’ dosing.

    Single-Dose Regimen for Uncomplicated Gonorrhea:     In clinical trials using a single 1,000 mg dose of cefuroxime axetil, 1,061 subjects were treated for uncomplicated gonorrhea.

    The adverse reactions in Table 6 were for subjects treated with a single dose of 1,000 mg cefuroxime axetil in U.S. clinical trials.


    Table 6. Adverse Reactions (≥1%) after Single-Dose Regimen with 1,000 mg   Cefuroxime Axetil Tablets for Uncomplicated Gonorrhea
    Adverse Reaction
    		Cefuroxime Axetil
    (n = 1,061)

    Gastrointestinal disorders     		 

      Nausea/Vomiting     		7%

      Diarrhea     		4%

    The following adverse reactions occurred in less than 1% but greater than 0.1% of subjects (n = 1,061) treated with a single dose of cefuroxime axetil 1,000 mg for uncomplicated gonorrhea in U.S. clinical trials.

        Infections and Infestations:     Vaginal candidiasis.

        Nervous System Disorders:     Headache, dizziness, somnolence.

        Cardiac Disorders:     Tightness/pain in chest, tachycardia.

        Gastrointestinal Disorders:     Abdominal pain, dyspepsia.

        Skin and Subcutaneous Tissue Disorders:     Erythema, rash, pruritus.

        Musculoskeletal and Connective Tissue Disorders:     Muscle cramps, muscle stiffness, muscle spasm of neck, lockjaw-type reaction.

        Renal and Urinary Disorders:     Bleeding/pain in urethra, kidney pain.

        Reproductive System and Breast Disorders:     Vaginal itch, vaginal discharge.

    6.2 Postmarketing Experience

    The following adverse reactions have been identified during post-approval use of cefuroxime axetil. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.


    Blood and Lymphatic System Disorders


    Hemolytic anemia, leukopenia, pancytopenia, thrombocytopenia.


    Gastrointestinal Disorders


    Pseudomembranous colitis [see Warnings and Precautions (5.2)] .


    Hepatobiliary Disorders


    Hepatic impairment including hepatitis and cholestasis, jaundice.


    Immune System Disorders


    Anaphylaxis, serum sickness-like reaction, acute myocardial ischemia with or without myocardial infarction may occur as part of an allergic reaction.

    Investigations


    Increased prothrombin time.


    Nervous System Disorders


    Seizure, encephalopathy.


    Renal and Urinary Disorders


    Renal dysfunction.


    Skin and Subcutaneous Tissue Disorders


    Angioedema, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, urticaria.

  • 7 DRUG INTERACTIONS

    7.1 Drugs that Reduce Gastric Acidity

    Drugs that reduce gastric acidity may result in a lower bioavailability of cefuroxime axetil compared with administration in the fasting state. Administration of drugs that reduce gastric acidity may negate the food effect of increased absorption of cefuroxime axetil when administered in the postprandial state. Administer cefuroxime axetil at least 1 hour before or 2 hours after administration of short-acting antacids. Histamine-2 (H 2) antagonists and proton pump inhibitors should be avoided.

    7.2 Probenecid

    Concomitant administration of probenecid with cefuroxime axetil tablets increases serum concentrations of cefuroxime [see Clinical Pharmacology (12.3)]. Coadministration of probenecid with cefuroxime axetil is not recommended.

    7.3 Drug/Laboratory Test Interactions

    A false-positive reaction for glucose in the urine may occur with copper reduction tests (e.g., Benedict's or Fehling's solution), but not with enzyme-based tests for glycosuria. As a false-negative result may occur in the ferricyanide test, it is recommended that either the glucose oxidase or hexokinase method be used to determine blood/plasma glucose levels in patients receiving cefuroxime axetil. The presence of cefuroxime does not interfere with the assay of serum and urine creatinine by the alkaline picrate method.

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary


    Available data from published epidemiologic studies, case series, and case reports over several decades with cephalosporin use, including cefuroxime axetil, in pregnant women have not established drug-associated risks of major birth defects, miscarriage, or adverse maternal or fetal outcomes (see Data). 

    In studies in pregnant mice and rats administered oral cefuroxime axetil during organogenesis at 14 and 9 times the maximum recommended human dose (MRHD) based on body surface area, respectively, there were no adverse developmental outcomes (see Data).

    The estimated background risk of major birth defects and miscarriage for the indicated populations are unknown. All pregnancies have a background risk of birth defects, loss, or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively. 

    Clinical Considerations

    Disease-Associated Maternal and/or Embryo/Fetal Risk:     Maternal gonorrhea may be associated with preterm birth, low neonatal birth weight, chorioamnionitis, intrauterine growth restriction, small for gestational age, and premature rupture of membranes. Perinatal transmission of gonorrhea to the offspring can result in infant blindness, joint infections, and bloodstream infections.

    Data

    Human Data:     While available studies cannot definitively establish the absence of risk, published data from epidemiologic studies, case series, and case reports over several decades have not identified an association with cephalosporin use (including cefuroxime axetil) during pregnancy and major birth defects, miscarriage, or other adverse maternal or fetal outcomes. Available studies have methodologic limitations, including small sample size, retrospective data collection, and inconsistent comparator groups. 

    Animal Data:     Studies performed with oral cefuroxime axetil administered to pregnant mice during organogenesis (Gestation Days 7 through 16) at doses up to 3,200 mg/kg/day (14 times the MRHD based on body surface area); and in rats dosed during organogenesis and lactation (Gestation Days 7 through 16 and Gestation Days 17 through Lactation Day 21, respectively) at doses up to 1,000 mg/kg/day (9 times the MRHD based on body surface area) have revealed no adverse developmental outcomes.

    8.2 Lactation

    Risk Summary


    Based on several published case reports describing multiple lactating women who received cefuroxime via intravenous, intramuscular, and oral routes, cefuroxime is present in human milk. The highest maternal milk concentration described occurred in lactating women 8 hours after an intramuscular administration of cefuroxime 750 mg. Allowing for an infant milk consumption of 150 mL/kg/day, the estimated breastfed infant dose would be less than 1% of the adult dose . No data are available on the effects of the drug on the breastfed infant or the effects of the drug on milk production. The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for cefuroxime and any potential adverse effects on the breastfed infant from cefuroxime or from the underlying maternal condition.

    8.4 Pediatric Use

    The safety and effectiveness of cefuroxime axetil have been established for pediatric patients aged 3 months to 12 years for acute bacterial maxillary sinusitis based upon its approval in adults. Use of cefuroxime axetil in pediatric patients is supported by pharmacokinetic and safety data in adults and pediatric patients, and by clinical and microbiological data from adequate and well-controlled trials of the treatment of acute bacterial maxillary sinusitis in adults and of acute otitis media with effusion in pediatric patients. It is also supported by postmarketing adverse events surveillance [see Indications and Usage (1), Dosage and Administration (2), Adverse Reactions (6), Clinical Pharmacology (12.3)].

    8.5 Geriatric Use

    Of the total number of subjects who received cefuroxime axetil in 20 clinical trials, 375 were aged 65 and older while 151 were aged 75 and older. No overall differences in safety or effectiveness were observed between these subjects and younger adult subjects. Reported clinical experience has not identified differences in responses between the elderly and younger adult patients, but greater sensitivity of some older individuals cannot be ruled out.


    Cefuroxime is substantially excreted by the kidney, and the risk of adverse reactions may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function.

    8.6 Renal Impairment

    Reducing the dosage of cefuroxime axetil is recommended for adult patients with severe renal impairment (creatinine clearance <30 mL/min) [see Dosage and Administration (2.5), Clinical Pharmacology (12.3)] .

  • 10 OVERDOSAGE

    Overdosage of cephalosporins can cause cerebral irritation leading to convulsions or encephalopathy. Serum levels of cefuroxime can be reduced by hemodialysis and peritoneal dialysis.

  • 11 DESCRIPTION

    Cefuroxime axetil tablets, USP contain cefuroxime as cefuroxime axetil. Cefuroxime axetil is a semisynthetic, cephalosporin antibacterial drug for oral administration.


    The chemical name of cefuroxime axetil (1-(acetyloxy) ethyl ester of cefuroxime) is ( RS)-1-hydroxyethyl (6 R,7 R)-7-[2-(2-furyl)glyoxyl-amido]-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]-oct-2-ene-2-carboxylate, 7 2-( Z)-( O-methyl-oxime), 1-acetate 3-carbamate. Its molecular formula is C 20H 22N 4O 10S, and it has a molecular weight of 510.48.


    Cefuroxime axetil is in the amorphous form and has the following structural formula:


    Chemical Structure

    Tablets are film-coated and contain the equivalent of 250 mg or 500 mg of cefuroxime as cefuroxime axetil USP. Tablets contain the inactive ingredients colloidal silicon dioxide, croscarmellose sodium, hydrogenated vegetable oil, hypromellose, microcrystalline cellulose, polyethylene glycol, sodium lauryl sulfate, and titanium dioxide.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Cefuroxime axetil is an antibacterial drug [see Microbiology (12.4)].

    12.3 Pharmacokinetics

    Absorption


    After oral administration, cefuroxime axetil is absorbed from the gastrointestinal tract and rapidly hydrolyzed by nonspecific esterases in the intestinal mucosa and blood to cefuroxime. Serum pharmacokinetic parameters for cefuroxime following administration of cefuroxime axetil tablets to adults are shown in Table 8.

    Table 8. Pharmacokinetics of Cefuroxime Administered in the Postprandial State as Cefuroxime Axetil Tablets to Adults a
    a  Mean values of 12 healthy adult volunteers.
    b  Drug administered immediately after a meal.
    Dose b (Cefuroxime Equivalent)
    		Peak Plasma Concentration (mcg/mL)
    		Time of Peak Plasma Concentration (h)
    		Mean Elimination Half-life (h)
    		AUC (mcg·h/mL)
    125 mg
    		2.1
    		2.2
    		1.2
    		6.7
    250 mg
    		4.1
    		2.5
    		1.2
    		12.9
    500 mg
    		7
    		3
    		1.2
    		27.4
    1,000 mg
    		13.6
    		2.5
    		1.3
    		50

    Effect of Food: Absorption of the tablet is greater when taken after food (absolute bioavailability increases from 37% to 52%). Despite this difference in absorption, the clinical and bacteriologic responses of subjects were independent of food intake at the time of tablet administration in 2 trials where this was assessed.

    Lack of Bioequivalence:     Oral suspension was not bioequivalent to tablets when tested in healthy adults. The tablet and oral suspension formulations are NOT substitutable on a milligram-per-milligram basis. The area under the curve for the suspension averaged 91% of that for the tablet, and the peak plasma concentration for the suspension averaged 71% of the peak plasma concentration of the tablets. Therefore, the safety and effectiveness of both the tablet and oral suspension formulations were established in separate clinical trials. 

    Distribution

    Cefuroxime is distributed throughout the extracellular fluids. Approximately 50% of serum cefuroxime is bound to protein. 

    Metabolism 

    The axetil moiety is metabolized to acetaldehyde and acetic acid.

    Excretion      

    Cefuroxime is excreted unchanged in the urine; in adults, approximately 50% of the administered dose is recovered in the urine within 12 hours. The pharmacokinetics of cefuroxime in pediatric subjects have not been studied. Until further data are available, the renal elimination of cefuroxime axetil established in adults should not be extrapolated to pediatric subjects.

    Specific Populations 

    Patients with Renal Impairment:     In a trial of 28 adults with normal renal function or severe renal impairment (creatinine clearance <30 mL/min), the elimination half-life was prolonged in relation to severity of renal impairment. Prolongation of the dosage interval is recommended in adult patients with creatinine clearance <30 mL/min [see Dosage and Administration (2.5)] .

    Geriatric Patients:     In a trial of 20 elderly subjects (mean age = 83.9 years) having a mean creatinine clearance of 34.9 mL/min, the mean serum elimination half-life was prolonged to 3.5 hours; however, despite the lower elimination of cefuroxime in geriatric patients, dosage adjustment based on age is not necessary [see Use in Specific Populations (8.5)] . 

    Drug Interaction Studies

    Concomitant administration of probenecid with cefuroxime axetil tablets increases the cefuroxime area under the serum concentration versus time curve and maximum serum concentration by 50% and 21%, respectively [see Drug Interactions (7.2)] .

    12.4 Microbiology

    Mechanism of Action


    Cefuroxime axetil is a bactericidal agent that acts by inhibition of bacterial cell wall synthesis. Cefuroxime axetil has activity in the presence of some β-lactamases, both penicillinases and cephalosporinases, of gram-negative and gram-positive bacteria.


    Resistance


    Resistance to cefuroxime axetil is primarily through hydrolysis by β-lactamase, alteration of penicillin-binding proteins (PBPs), decreased permeability, and the presence of bacterial efflux pumps.


    Susceptibility to cefuroxime axetil will vary with geography and time; local susceptibility data should be consulted, if available. Beta-lactamase -negative, ampicillin-resistant (BLNAR) isolates of H. influenzae should be considered resistant to cefuroxime axetil.

    Antimicrobial Activity

    Cefuroxime axetil has been shown to be active against most isolates of the following bacteria, both in vitro and in clinical infections [see Indications and Usage (1)] :


    Aerobic Bacteria:


    Gram-positive bacteria

    • Staphylococcus aureus (methicillin-susceptible isolates only)
    • Streptococcus pneumoniae
    • Streptococcus pyogenes

    Gram-negative bacteria

    • Escherichia colia
    • Klebsiella pneumoniaea
    • Haemophilus influenzae
    • Haemophilus parainfluenzae
    • Moraxella catarrhalis
    • Neisseria gonorrhoeae

    a          Most extended spectrum β-lactamase (ESBL) -producing and carbapenemase-producing isolates are resistant to cefuroxime axetil.

    Spirochetes

    • Borrelia burgdorferi

    The following in vitro data are available, but their clinical significance is unknown. At least 90 percent of the following bacteria exhibit an in vitro minimum inhibitory concentration (MIC) less than or equal to the susceptible breakpoint for cefuroxime against isolates of similar genus or organism group. However, the efficacy of cefuroxime axetil in treating clinical infections caused by these bacteria has not been established in adequate and well-controlled clinical trials.


    Aerobic Bacteria:


    Gram-positive bacteria

    • Staphylococcus epidermidis (methicillin-susceptible isolates only)
    • Staphylococcus saprophyticus (methicillin-susceptible isolates only)
    • Streptococcus agalactiae

    Gram-negative bacteria

    • Morganella morganii
    • Proteus inconstans
    • Proteus mirabilis
    • Providencia rettgeri

    Anaerobic Bacteria:

    Gram-positive bacteria

    • Peptococcus niger

    Susceptibility Testing


    For specific information regarding susceptibility test interpretive criteria and associated test methods and quality control standards recognized by FDA for this drug, please see: https://www.fda.gov/STIC.

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    Although lifetime studies in animals have not been performed to evaluate carcinogenic potential, no mutagenic activity was found for cefuroxime axetil in a battery of bacterial mutation tests. Positive results were obtained in an in vitro chromosome aberration assay; however, negative results were found in an in vivo micronucleus test at doses up to 1.5 g/kg. Fertility studies in rats (males dosed for 70 days prior to and through mating; females dosed 21 days prior to mating through lactation) at doses up to 1,000 mg/kg/day (9 times the MRHD based on body surface area) have revealed no adverse effects on fertility.

  • 14 CLINICAL STUDIES

    14.1 Acute Bacterial Maxillary Sinusitis

    One adequate and well-controlled trial was performed in subjects with acute bacterial maxillary sinusitis. In this trial, each subject had a maxillary sinus aspirate collected by sinus puncture before treatment was initiated for presumptive acute bacterial sinusitis. All subjects had radiographic and clinical evidence of acute maxillary sinusitis. In the trial, the clinical effectiveness of cefuroxime axetil in treating acute maxillary sinusitis was comparable to an oral antimicrobial agent containing a specific β-lactamase inhibitor. However, microbiology data demonstrated cefuroxime axetil to be effective in treating acute bacterial maxillary sinusitis due only to Streptococcus pneumoniae or non-β-lactamase–producing Haemophilus influenzae. Insufficient numbers of β-lactamase–producing Haemophilus influenzae and Moraxella catarrhalis isolates were obtained in this trial to adequately evaluate the effectiveness of cefuroxime axetil in treating acute bacterial maxillary sinusitis due to these 2 organisms.


    This trial randomized 317 adult subjects, 132 subjects in the U.S. and 185 subjects in South America. Table 10 shows the results of the intent-to-treat analysis.

    Table 10. Clinical Effectiveness of Cefuroxime Axetil Tablets in the Treatment of Acute Bacterial Maxillary Sinusitis
    a 95% confidence interval around the success difference [-0.08, +0.32].
    b 95% confidence interval around the success difference [-0.1, +0.16].
    c Control was an antibacterial drug containing a β-lactamase inhibitor.
    U.S. Subjects a
    		South American Subjects b
    Cefuroxime Axetil
    250 mg Twice
    Daily
    (n = 49)
    		Control c
    (n = 43)
    		Cefuroxime Axetil
    250 mg Twice
    Daily
    (n = 49)
    		Control c
    (n = 43)
    Clinical success
    (cure + improvement)
    		65%
    		53%
    		77%
    		74%
    Clinical cure
    		53%
    		44%
    		72%
    		64%
    Clinical improvement
    		12%
    		9%
    		5%
    		10%

    In this trial and in a supporting maxillary puncture trial, 15 evaluable subjects had non-β-lactamase–producing Haemophilus influenzae as the identified pathogen. Of these, 67% (10/15) had this pathogen eradicated. Eighteen (18) evaluable subjects had Streptococcus pneumoniae as the identified pathogen. Of these, 83% (15/18) had this pathogen eradicated.

    14.2 Early Lyme Disease

    Two adequate and well-controlled trials were performed in subjects with early Lyme disease. All subjects presented with physician-documented erythema migrans, with or without systemic manifestations of infection. Subjects were assessed at 1 month posttreatment for success in treating early Lyme disease (Part I) and at 1 year posttreatment for success in preventing the progression to the sequelae of late Lyme disease (Part II).


    A total of 355 adult subjects (181 treated with cefuroxime axetil and 174 treated with doxycycline) were randomized in the 2 trials, with diagnosis of early Lyme disease confirmed in 79% (281/355). The clinical diagnosis of early Lyme disease in these subjects was validated by 1) blinded expert reading of photographs, when available, of the pretreatment erythema migrans skin lesion, and 2) serologic confirmation (using enzyme-linked immunosorbent assay [ELISA] and immunoblot assay [“Western” blot]) of the presence of antibodies specific to Borrelia burgdorferi, the etiologic agent of Lyme disease. The efficacy data in Table 11 are specific to this “validated” patient subset, while the safety data below reflect the entire patient population for the 2 trials. Clinical data for evaluable subjects in the “validated” patient subset are shown in Table 11.

    Table 11. Clinical Effectiveness of Cefuroxime Axetil Tablets Compared with Doxycycline in the Treatment of Early Lyme Disease
    a 95% confidence interval around the satisfactory difference for Part I (-0.08, +0.05).
    b 95% confidence interval around the satisfactory difference for Part II (-0.13, +0.07).
    c n’s include subjects assessed as unsatisfactory clinical outcomes (failure + recurrence) in  Part I (cefuroxime axetil - 11 [5 failure, 6 recurrence]; doxycycline - 8 [6 failure, 2 recurrence]).
    d Satisfactory clinical outcome includes cure + improvement (Part I) and success + improvement (Part II).
    Part I
    (1 Month after 20 Days of Treatment) a
    		Part II
    (1 Year after 20 Days of Treatment) b
    Cefuroxime Axetil
    500 mg Twice
    Daily
    (n = 125)
    		Doxycycline 100 mg 3 Times Daily (n = 108)
    		Cefuroxime Axetil
    500 mg Twice
    Daily
    (n = 105 c)
    		Doxycycline 100 mg 3 Times Daily (n = 83 c)
    Satisfactory clinical outcome d
    		91%
    		93%
    		84%
    		87%
    Clinical cure/success
    		72%
    		73%
    		73%
    		73%
    Clinical improvement
    		19%
    		19%
    		10%
    		13%

    Cefuroxime axetil and doxycycline were effective in prevention of the development of sequelae of late Lyme disease.


    While the incidence of drug-related gastrointestinal adverse reactions was similar in the 2 treatment groups (cefuroxime axetil - 13%; doxycycline - 11%), the incidence of drug-related diarrhea was higher in the cefuroxime axetil arm versus the doxycycline arm (11% versus 3%, respectively).

  • 16 HOW SUPPLIED/STORAGE AND HANDLING




    Cefuroxime Axetil Tablets USP, 500 mg of cefuroxime (as cefuroxime axetil), are white to off-white, film-coated, capsule shaped tablets with ‘A34’ debossed on one side and plain on the other side.



    20 Tablets/Bottle NDC: 68071-2958-2



    Store at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. Replace cap securely after each opening.

  • 17 PATIENT COUNSELING INFORMATION

    Allergic Reactions

    Inform patients that cefuroxime axetil is a cephalosporin that can cause allergic reactions in some individuals [see Warnings and Precautions (5.1)] .

    Clostridioides difficile     -Associated Diarrhea

    Inform patients that diarrhea is a common problem caused by antibacterials, and it usually ends when the antibacterial is discontinued. Sometimes after starting treatment with antibacterials, patients can develop watery and bloody stools (with or without stomach cramps and fever) even as late as 2 or more months after having taken their last dose of the antibacterial. If this occurs, advise patients to contact their physician as soon as possible.

    Crushing Tablets      

    Instruct patients to swallow the tablet whole, without crushing the tablet. Patients who cannot swallow the tablet whole should receive the oral suspension.
                                                                                                     

    Drug Resistance

    Inform patients that antibacterial drugs, including cefuroxime axetil, should only be used to treat bacterial infections. They do not treat viral infections (e.g., the common cold). When cefuroxime axetil is prescribed to treat a bacterial infection, inform patients that although it is common to feel better early in the course of therapy, the medication should be taken exactly as directed. Skipping doses or not completing the full course of therapy may: (1) decrease the effectiveness of the immediate treatment, and (2) increase the likelihood that bacteria will develop resistance and will not be treatable by cefuroxime axetil or other antibacterial drugs in the future.

    Distributed by:
    Rising Health, LLC
    Saddle Brook, NJ 07663
    Made in India

    Code: TS/DRUGS/78/1996

    Revised: 04/2021

  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL

    pdp

  • INGREDIENTS AND APPEARANCE
    CEFUROXIME AXETIL 
    cefuroxime axetil tablet, film coated
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 68071-2958(NDC:57237-059)
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CEFUROXIME AXETIL (UNII: Z49QDT0J8Z) (CEFUROXIME - UNII:O1R9FJ93ED) CEFUROXIME500 mg
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    HYDROGENATED COTTONSEED OIL (UNII: Z82Y2C65EA)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    Colorwhite (White to Off-white) Scoreno score
    ShapeOVAL (CAPSULE-SHAPED) Size20mm
    FlavorImprint Code A34
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 68071-2958-220 in 1 BOTTLE; Type 0: Not a Combination Product03/20/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA06530803/29/2006
    Labeler - NuCare Pharmaceuticals,Inc. (010632300)
    Establishment
    NameAddressID/FEIBusiness Operations
    Aurobindo Pharma Limited010632300relabel(68071-2958)
    • © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.