Pronunciation:
(SEF a klor)
U.S. Brand Names:
Ceclor®; Ceclor® CD; Raniclor™
Generic Available:
Yes
Canadian Brand Names:
Apo-Cefaclor®; Ceclor®; Novo-Cefaclor; Nu-Cefaclor; PMS-Cefaclor
Use:
Treatment of susceptible bacterial infections including otitis media, lower respiratory tract infections, acute exacerbations of chronic bronchitis, pharyngitis and tonsillitis, urinary tract infections, skin and skin structure infections
Use - Dental:
Alternative antibiotic for treatment of orofacial infections in patients allergic to penicillins; susceptible bacteria including aerobic gram-positive bacteria and anaerobes
Pregnancy Risk Factor:
B
Lactation:
Enters breast milk/use caution
Contraindications:
Hypersensitivity to cefaclor, any component of the formulation, or other cephalosporins
Warnings/Precautions:
Modify dosage in patients with severe renal impairment. Prolonged use may result in superinfection. Use with caution in patients with a history of penicillin allergy especially IgE-mediated reactions (eg, anaphylaxis, urticaria). Beta-lactamase-negative, ampicillin-resistant (BLNAR) strains of H. influenzae should be considered resistant to cefaclor. Extended release tablets are not approved for use in children <16 years of age.
Adverse Reactions:
1% to 10%:
Dermatologic: Rash (maculopapular, erythematous, or morbilliform) (1% to 2%)
Gastrointestinal: Diarrhea (3%)
Genitourinary: Vaginitis (2%)
Hematologic: Eosinophilia (2%)
Hepatic: Transaminases increased (3%)
Miscellaneous: Moniliasis (2%)
<1%: Agitation, agranulocytosis, anaphylaxis, angioedema, aplastic anemia, arthralgia, cholestatic jaundice, CNS irritability, confusion, dizziness, hallucinations, hemolytic anemia, hepatitis, hyperactivity, insomnia, interstitial nephritis, nausea, nervousness, neutropenia, paresthesia, pruritus, pseudomembranous colitis, PT prolonged, seizure, serum-sickness, somnolence, Stevens-Johnson syndrome, urticaria, thrombocytopenia, toxic epidermal necrolysis, vomiting
Reactions reported with other cephalosporins include fever, abdominal pain, superinfection, renal dysfunction, toxic nephropathy, hemorrhage, cholestasis
Overdosage/Toxicology:
Symptoms of overdose include diarrhea, epigastric distress, nausea, and vomiting. Many beta-lactam containing antibiotics have the potential to cause neuromuscular hyperirritability or seizures. Hemodialysis may be helpful to aid in removal of the drug from blood; otherwise, treatment is supportive and symptom-directed.
Drug Interactions:
Aminoglycosides: May be additive to nephrotoxicity.
Furosemide: May be additive to nephrotoxicity.
Probenecid: May decrease cephalosporin elimination.
Ethanol/Nutrition/Herb Interactions:
Food: Cefaclor serum levels may be decreased slightly if taken with food. The bioavailability of cefaclor extended release tablets is decreased 23% and the maximum concentration is decreased 67% when taken on an empty stomach.
Stability:
Store at controlled room temperature. Refrigerate suspension after reconstitution. Discard after 14 days. Do not freeze.
Mechanism of Action:
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.
Pharmacodynamics/Kinetics:
Absorption: Well absorbed, acid stable
Distribution: Widely throughout the body and reaches therapeutic concentration in most tissues and body fluids, including synovial, pericardial, pleural, peritoneal fluids; bile, sputum, and urine; bone, myocardium, gallbladder, skin and soft tissue; crosses placenta; enters breast milk
Protein binding: 25%
Metabolism: Partially hepatic
Half-life elimination: 0.5-1 hour; prolonged with renal impairment
Time to peak: Capsule: 60 minutes; Suspension: 45 minutes
Excretion: Urine (80% as unchanged drug)
Dosage:
Oral:
Children >1 month: Dosing range: 20-40 mg/kg/day divided every 8-12 hours; maximum dose: 1 g/day
Otitis media: 40 mg/kg/day divided every 12 hours
Pharyngitis: 20 mg/kg/day divided every 12 hours
Adults: Dosing range: 250-500 mg every 8 hours
Extended release tablets:
Acute bacterial exacerbations of or secondary infections with chronic bronchitis: 500 mg every 12 hours for 7 days
Pharyngitis, tonsillitis, uncomplicated skin and skin structure infections: 375 mg every 12 hours for 10 days
Dosing adjustment in renal impairment:
Clcr 10-50 mL/minute: Administer 50% to 100% of dose
Clcr<10 mL/minute: Administer 50% of dose
Hemodialysis: Moderately dialyzable (20% to 50%)
Administration:
Administer around-the-clock to promote less variation in peak and trough serum levels.
Chewable tablet: Should be chewed before swallowing; should not be swallowed whole
Extended release tablet: Should not be cut, crushed, or chewed; should be administered with food
Oral suspension: Shake well before using.
Monitoring Parameters:
Assess patient at beginning and throughout therapy for infection; monitor for signs of anaphylaxis during first dose
Test Interactions:
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
Dietary Considerations:
Capsule, chewable tablet, and suspension may be taken with or without food. Extended release tablet should be taken with food. Raniclor™ contains phenylalanine 2.8 mg/cefaclor 125 mg.
Patient Education:
Inform prescriber of all prescriptions, OTC medications, or herbal products you are taking, and any allergies you have. Do not take any new medication during therapy unless approved by prescriber. Take as directed, at regular intervals around-the-clock (with or without food). Chilling oral suspension improves flavor (do not freeze). Do not chew or crush extended release tablets. Maintain adequate hydration (2-3 L/day of fluids) unless instructed to restrict fluid intake. Complete full course of medication, even if you feel better. May cause false test results with Clinitest®; use of another type of testing is preferable. May cause diarrhea (yogurt, boiled milk, or buttermilk may help). Report rash; respiratory difficulty or swallowing; persistent nausea, vomiting, or abdominal pain; changes in urinary pattern or pain on urination; opportunistic infection (eg, vaginal itching or drainage; sores in mouth; blood in stool or urine, vaginal itching or drainage, unusual fever or chills); or CNS changes (eg, irritability, agitation, nervousness, insomnia, hallucinations). Breast-feeding precaution: Consult prescriber if breast-feeding.
Dental Health: Effects on Dental Treatment:
No significant effects or complications reported
Dental Health: Vasoconstrictor/Local Anesthetic Precautions:
No information available to require special precautions
Dental Comment:
Patients allergic to penicillins can use a cephalosporin; the incidence of cross-reactivity between penicillins and cephalosporins is 1% when the allergic reaction to penicillin is delayed. Cefaclor is effective against anaerobic bacteria, but the sensitivity of alpha-hemolytic Streptococcus vary; approximately 10% of strains are resistant. Nearly 70% are intermediately sensitive. If the patient has a history of immediate reaction to penicillin, the incidence of cross-reactivity is 20%; cephalosporins are contraindicated in these patients.
Mental Health: Effects on Mental Status:
May cause nervousness; case reports of euphoria, delusion, illusions, and depersonalization with cephalosporins
Mental Health: Effects on Psychiatric Treatment:
May rarely cause neutropenia; use caution with clozapine and carbamazepine
Dosage Forms:
Capsule (Ceclor®): 250 mg, 500 mg
Powder for oral suspension: 125 mg/5 mL (75 mL, 150 mL); 187 mg/5 mL (50 mL, 100 mL); 250 mg/5 mL (75 mL, 150 mL); 375 mg/5 mL (50 mL, 100 mL)
Ceclor®: 125 mg/5 mL (150 mL); 187 mg/5 mL (100 mL); 250 mg/5 mL (75 mL, 150 mL); 375 mg/5 mL (100 mL)
Tablet, chewable (Raniclor™): 125 mg [contains phenylalanine 2.8 mg; fruity flavor], 187 mg [contains phenylalanine 4.2 mg; fruity flavor], 250 mg [contains phenylalanine 5.6 mg; fruity flavor], 375 mg [contains phenylalanine 8.4 mg; fruity flavor]
Tablet, extended release (Ceclor® CD): 375 mg, 500 mg
International Brand Names:
Adco-Cefaclor® (ZA); Alfacet® (YU); Alfatil® (FR); Altaclor® (IT); Apo-Cefaclor® (CA, PL); Bactigram® (IT); Biocef® (BD); Capabiotic® (ID); CEC® (AT, CZ, DE, DO, LU, RO, ZA); Ceclodyne® (RO); Ceclor® (AT, AU, BD, BE, BR, CA, CH, CO, CR, CZ, DO, ES, GT, HN, HR, HU, ID, IL, LU, MX, NL, NZ, PA, PL, PT, RO, RU, SI, SV, TR, ZA); Ceclorbeta® (DE); Cecloretta® (HU); Ceclor® MR (RO); Cefabac® (BG, JO, KW, LB, MA, MY, SY); Cefaclor 1A Pharma® (DE); Cefaclor ABC® (IT); Cefaclor acis® (DE); Cefaclor Ahimsa® (AR); Cefaclor AL® (DE); Cefaclor AZU® (DE); Cefaclor Basics® (DE); Cefaclor beta® (DE); Cefaclor Bexal® (ES); Cefaclor Biochemie® (CO, RO); Cefaclor® (CZ, GB, RO); Cefaclor DOC® (IT); Cefaclor EG® (IT); Cefaclor Fabra® (AR); Cefaclor Heumann® (DE); Cefaclor K24® (IT); Cefaclor Lindo® (DE); Cefaclor Merck® (IT); Cefaclor MK® (CR, DO, GT, HN, PA, SV); Cefaclor Normon® (ES); Cefaclor PB® (DE); Cefaclor Pliva® (IT); Cefaclor Ranbaxy® (ES); Cefaclor-ratiopharm® (DE, HU, IT); Cefaclor Richet® (AR); Cefaclor S250 Stada® (TH); Cefaclor Sandoz® (DE); Cefaclor Stada® (DE); Cefaclor-Teva® (IL); Cefaclor-Wolff® (DE); CefaCl® (SI); Cefager® (IE); Cefahexal® (AT); Cefaklor® (YU); Cefalcor® (IT); Cefalor® (IL); Cefaltrex® (DO); Cefamid® (DO); Cefastad® (AT); Cef-Diolan® (DE); Cefin® (DO); Cefkor® (AU); Cefor® (PL); Cefral® (AR); Cefulton® (IT); CEK® (PL); Celco® (TH); cephaclor von ct® (DE); Cephalodoc® (DE); Citiclor® (IT); Cleancef® (SG); Cloracef® (HK, ID, JO, KW, LB, MT, MY, RO, ZA); Clorad® (IT); Clorazer® (IT); Clorotir® (NZ); DBL Cefaclor® (AU); Distaclor® (GB, HK, IE, SG, TH); Dista MR® (GB); Doccefaclo® (BE); Dorf® (IT); Especlor® (ID); Eurocefix® (IT); Faclor® (BR); Falcef® (DO); Fuclode® (IT); Geniclor® (IT); hefa clor® (DE); Infectocef® (DE); Kefaclor® (TH); Keflor® (AU, CL, IN); Kefolor® (FI); Kefsid® (TR); Keftid® (GB, IE); Kliacef® (IT); Kloracef® (PL); KWICap® (AR); Lafarclor® (IT); Lilly-Cefaclor® (ZA); Loracef® (BD); Losefar® (TR); Medikoncef® (ID); Medoclor® (RO); Navacef® (BD); Necloral® (IT); Novacef® (BR); Novo-Cefaclor (CA); Nu-Cefaclor (CA); Oralcef® (IT); Panacef® (IT); Panclor® (PL); Panoral® (DE); Performer® (IT); Pinaclor® (IE); PMS-Cefaclor (CA); Razicef® (BG); Remeclor® (CY); Rolab-Cefaclor® (ZA); Selviclor® (IT); Serviclor® (CZ, PL); Sifaclor® (TH); Sigacefal® [caps.] (DE); Sinclor® (RO); Soficlor® (SG); Suclor® (DO); Taracef® (PL, RU, SI); Tibifor® (IT); Vercef® (CZ, HU, PL, RO, RU, SG, TH, ZA); Vercef MR® (CZ, HU, PL)
References
American Thoracic Society, "Guidelines for the Initial Management of Adults With Community-Acquired Pneumonia: Diagnosis, Assessment of Severity, and Initial Antimicrobial Therapy,"Am Rev Respir Dis, 1993, 148(5):1418-26.
Boguniewicz M and Leung DYM, "Hypersensitivity Reactions to Antibiotics Commonly Used in Children,"Pediatr Infect Dis J, 1995, 14(3):221-31.
Donowitz GR and Mandell GL, "Beta-Lactam Antibiotics,"N Engl J Med, 1988, 318(7):419-26 and 318(8):490-500.
Hyslop DL, "Cefaclor Safety Profile: A Ten Year Review,"Clin Ther, 1988, 11(Suppl A):83-94.
Levine LR, "Quantitative Comparison of Adverse Reactions to Cefaclor vs Amoxicillin in a Surveillance Study,"Pediatr Infect Dis, 1985, 4(4):358-61.
Marshall WF and Blair JE, "The Cephalosporins,"Mayo Clin Proc, 1999, 74(2):187-95.
Saxon A, Beall GN, Rohr AS, et al, "Immediate Hypersensitivity Reactions to Beta-Lactam Antibiotics,"Ann Intern Med, 1987, 107(2):204-15.
Smith GH, "Oral Cephalosporins in Perspective,"DICP, 1990, 24(1):45-51.
Wright AJ, "The Penicillins,"Mayo Clin Proc, 1999, 74(3):290-307.