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- Cefadroxil Monohydrate
Excipient information presented when available (limited, particularly for generics); consult specific product labeling.
Generic: 500 mg
Suspension Reconstituted, Oral:
Generic: 250 mg/5 mL (100 mL); 500 mg/5 mL (75 mL, 100 mL)
Generic: 1 g
- Antibiotic, Cephalosporin (First Generation)
Inhibits bacterial cell wall synthesis by binding to one or more of the penicillin-binding proteins (PBPs) which in turn inhibits the final transpeptidation step of peptidoglycan synthesis in bacterial cell walls, thus inhibiting cell wall biosynthesis. Bacteria eventually lyse due to ongoing activity of cell wall autolytic enzymes (autolysins and murein hydrolases) while cell wall assembly is arrested.
Rapid and well absorbed from GI tract
Vd: 0.31 L/kg
Urine (>90% as unchanged drug within 24 hours)
Time to Peak
Serum: Within 70 to 90 minutes
1 to 2 hours; 20 to 24 hours in renal failure
Use: Labeled Indications
Pharyngitis and/or tonsillitis: Treatment of pharyngitis and/or tonsillitis caused by Streptococcus pyogenes (group A beta-hemolytic streptococci).
Skin and skin structure infections: Treatment of skin and skin structure infections caused by staphylococci and/or streptococci.
Urinary tract infection: Treatment of urinary tract infections caused by Escherichia coli, Proteus mirabilis, and Klebsiella species.
Chronic oral antimicrobial suppression of prosthetic joint infection with Staphylococci (oxacillin-susceptible) after completion of parenteral therapy
Hypersensitivity to cefadroxil, any component of the formulation, or other cephalosporins
Usual dosage range: Oral:
Children: 30 mg/kg/day divided every 12 hours (maximum: 2000 mg daily)
Adults: 1-2 g daily in a single dose or 2 divided doses
Indication-specific dosing: Oral:
Pharyngitis, group A streptococci (IDSA guidelines): Children and Adults: 30 mg/kg once daily (maximum: 1 g daily) for 10 days (Shulman, 2012). Note: Recommended as an alternative agent in penicillin-allergic patients; however, avoid in patients with immediate type hypersensitivity to penicillin.
Prosthetic joint infection, chronic oral antimicrobial suppression, staphylococci (oxacillin-susceptible) (preferred) (off-label use): Adults: 500 mg every 12 hours (Osmon, 2013)
Skin and skin structure infections: Adults: 1 g daily in a single or 2 divided doses
Tonsillitis: Adults: 1 g daily in a single or 2 divided doses for 10 days
Urinary tract infections: Adults: 1 g twice daily. For uncomplicated infections: 1 or 2 g daily in a single or 2 divided doses
Dosage adjustment in renal impairment:
CrCl 25-50 mL/minute: Administer every 12 hours
CrCl 10-25 mL/minute: Administer every 24 hours
CrCl <10 mL/minute: Administer every 36 hours
Dosage adjustment in hepatic impairment: No dosage adjustment provided in manufacturer’s labeling.
Powder for suspension: Refer to manufacturer’s product labeling for reconstitution instructions. Shake vigorously until suspended.
Administer around-the-clock to promote less variation in peak and trough serum levels. Administer without regards to meals; administration with food may diminish GI complaints.
Store capsules, tablets and un-reconstituted oral suspension at 20°C to 25°C (68°F to 77F); excursions are permitted to 15°C to 30°C (59°F to 86°F). After reconstitution, oral suspension may be stored for 14 days under refrigeration (4°C).
BCG (Intravesical): Antibiotics may diminish the therapeutic effect of BCG (Intravesical). Avoid combination
BCG Vaccine (Immunization): Antibiotics may diminish the therapeutic effect of BCG Vaccine (Immunization). Monitor therapy
Probenecid: May increase the serum concentration of Cephalosporins. Monitor therapy
Sodium Picosulfate: Antibiotics may diminish the therapeutic effect of Sodium Picosulfate. Management: Consider using an alternative product for bowel cleansing prior to a colonoscopy in patients who have recently used or are concurrently using an antibiotic. Consider therapy modification
Typhoid Vaccine: Antibiotics may diminish the therapeutic effect of Typhoid Vaccine. Only the live attenuated Ty21a strain is affected. Management: Vaccination with live attenuated typhoid vaccine (Ty21a) should be avoided in patients being treated with systemic antibacterial agents. Use of this vaccine should be postponed until at least 3 days after cessation of antibacterial agents. Consider therapy modification
Vitamin K Antagonists (eg, warfarin): Cephalosporins may enhance the anticoagulant effect of Vitamin K Antagonists. Monitor therapy
Positive direct Coombs', false-positive urinary glucose test using cupric sulfate (Benedict's solution, Clinitest®, Fehling's solution), false-positive serum or urine creatinine with Jaffé reaction
1% to 10%: Gastrointestinal: Diarrhea
<1% (Limited to important or life-threatening): Agranulocytosis, anaphylaxis, angioedema, cholestasis, Clostridium difficile associated diarrhea, dyspepsia, erythema multiforme, erythematous rash, genital candidiasis, hepatic failure, increased serum transaminases, maculopapular rash, neutropenia, pseudomembranous colitis, serum sickness, Stevens-Johnson syndrome, thrombocytopenia, vaginitis
Concerns related to adverse effects:
• Penicillin allergy: Use with caution in patients with a history of penicillin allergy, especially IgE-mediated reactions (eg, anaphylaxis, angioedema, urticaria).
• Superinfection: Prolonged use may result in fungal or bacterial superinfection, including C. difficile-associated diarrhea (CDAD) and pseudomembranous colitis; CDAD has been observed >2 months postantibiotic treatment.
• Colitis: Use with caution in patients with a history of gastrointestinal disease, particularly colitis.
• Renal impairment: Use with caution in patients with renal impairment (CrCl <50 mL/minute/1.73 m2); modify dosage in severe impairment.
Dosage form specific issues:
• Benzyl alcohol and derivatives: Some dosage forms may contain sodium benzoate/benzoic acid; benzoic acid (benzoate) is a metabolite of benzyl alcohol; large amounts of benzyl alcohol (≥99 mg/kg/day) have been associated with a potentially fatal toxicity (“gasping syndrome”) in neonates; the “gasping syndrome” consists of metabolic acidosis, respiratory distress, gasping respirations, CNS dysfunction (including convulsions, intracranial hemorrhage), hypotension, and cardiovascular collapse (AAP ["Inactive" 1997]; CDC, 1982); some data suggests that benzoate displaces bilirubin from protein binding sites (Ahlfors, 2001); avoid or use dosage forms containing benzyl alcohol derivative with caution in neonates. See manufacturer’s labeling.
• Suspension: May contain sulfur dioxide (sulfite); hypersensitivity reactions, including anaphylaxis and/or asthmatic exacerbations, may occur (may be life threatening).
• Appropriate use: Only IM penicillin has been shown to be effective in the prophylaxis of rheumatic fever. Cefadroxil is generally effective in the eradication of streptococci from the oropharynx; efficacy data for cefadroxil in the prophylaxis of subsequent rheumatic fever episodes are not available.
Monitor renal function. Observe for signs and symptoms of anaphylaxis during first dose.
Pregnancy Risk Factor
Adverse events have not been observed in animal reproduction studies. Cefadroxil crosses the placenta. Limited data is available concerning the use of cefadroxil in pregnancy; however, adverse fetal effects were not noted in a small clinical trial.
• Discuss specific use of drug and side effects with patient as it relates to treatment. (HCAHPS: During this hospital stay, were you given any medicine that you had not taken before? Before giving you any new medicine, how often did hospital staff tell you what the medicine was for? How often did hospital staff describe possible side effects in a way you could understand?)
• Patient may experience diarrhea. Have patient report immediately to prescriber signs of hepatic impairment, chills, pharyngitis, considerable asthenia, urinary retention, oliguria, vaginitis, or signs of pseudomembranous colitis (rare) (HCAHPS).
• Educate patient about signs of a significant reaction (eg, wheezing; chest tightness; fever; itching; bad cough; blue skin color; seizures; or swelling of face, lips, tongue, or throat). Note: This is not a comprehensive list of all side effects. Patient should consult prescriber for additional questions.
Intended Use and Disclaimer: Should not be printed and given to patients. This information is intended to serve as a concise initial reference for healthcare professionals to use when discussing medications with a patient. You must ultimately rely on your own discretion, experience and judgment in diagnosing, treating and advising patients.
More about cefadroxil
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- Cefadroxil (FDA)
- Cefadroxil Capsules (FDA)
- Cefadroxil Oral Suspension (FDA)
- Other brands: Duricef