Cefadroxil: Difference between revisions
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==General== | ==General== | ||
*Type: | *Type: [[Is Generation::1st generation]] [[Is DrugClass::cephalosporin]] | ||
*Dosage Forms: | *Dosage Forms: capsule, oral suspension, tablet | ||
*Common Trade Names: Duricef | *Dosage Strengths: capsule: 500mg; oral suspension: 250mg/5mL, 500mg/5mL; tablet: 1g | ||
*Routes of Administration: PO | |||
*Common Trade Names: Duricef, Ultracef | |||
==Adult Dosing== | ==Adult Dosing== | ||
===Infections, | ===Infections, [[bacterial]]=== | ||
*1-2g/day PO divided q12-24h | *1-2g/day PO divided q12-24h | ||
| Line 12: | Line 14: | ||
==Pediatric Dosing== | ==Pediatric Dosing== | ||
===Infections, [[bacterial]]=== | |||
*30mg/kg/day PO divided q12-24h max 2g/day | |||
===[[Pharyngitis]]/[[tonsillitis]], [[streptococcal]]=== | |||
* | *30mg/kg/day PO divided q12-24h x 10days, max 1g/day | ||
==Special Populations== | ==Special Populations== | ||
| Line 61: | Line 63: | ||
*dyspepsia | *dyspepsia | ||
*urticaria | *urticaria | ||
* | *pruritus | ||
*rash | *rash | ||
*vomiting | *vomiting | ||
| Line 203: | Line 205: | ||
<references/> | <references/> | ||
[[Category:Pharmacology]] | [[Category:Pharmacology]] [[Category:ID]] | ||
Latest revision as of 16:07, 18 July 2025
General
- Type: 1st generation cephalosporin
- Dosage Forms: capsule, oral suspension, tablet
- Dosage Strengths: capsule: 500mg; oral suspension: 250mg/5mL, 500mg/5mL; tablet: 1g
- Routes of Administration: PO
- Common Trade Names: Duricef, Ultracef
Adult Dosing
Infections, bacterial
- 1-2g/day PO divided q12-24h
Pharyngitis/tonsillitis, streptococcal
- 1g PO divided q12-24h x 10days
Pediatric Dosing
Infections, bacterial
- 30mg/kg/day PO divided q12-24h max 2g/day
Pharyngitis/tonsillitis, streptococcal
- 30mg/kg/day PO divided q12-24h x 10days, max 1g/day
Special Populations
- Pregnancy Rating: B (no evidence of harm)
- Lactation: safe (no risk/minimal risk)
- Renal Dosing
- Adult
- GFR 25-50: 1g x1, then 500mg q12h
- GFR 10-25: 1g x1 then 500mg q24h
- GFR < 10: 1g x1, then 500mg q36h
- HD: give 0.5-1g supplement
- PD: 500mg q24h
- Pediatric
- GFR 10-25: give q24h
- GFR < 10: give q36h
- HD: give supplement
- PD: no supplement
- Adult
- Hepatic Dosing
- Adult: not defined
- Pediatric: not defined
Contraindications
- Allergy to class/drug
Adverse Reactions
Serious
- anaphylaxis
- Stevens-Johnson syndrome
- toxic epidermal necrolysis
- angioedema
- neutropenia
- thrombocytopenia
- pancytopenia
- anemia, hemolytic
- aplastic anemia
- hemorrhage
- seizures
- superinfection
- C.difficile-associated diarrhea
Common
- diarrhea
- nausea
- dyspepsia
- urticaria
- pruritus
- rash
- vomiting
- ALT, AST elevation
Pharmacology
- Half-life:
- 78-96 min, 20-25hr (ESRD)
- Metabolism:
- minimal, site unknown
- Excretion:
- urine primarily (>90% unchanged)
- Mechanism of Action:
- bacteriacidal; inhibits cell wall mucopeptide synthesis
Antibiotic Sensitivities[1]
Key
- S susceptible/sensitive (usually)
- I intermediate (variably susceptible/resistant)
- R resistant (or not effective clinically)
- S+ synergistic with cell wall antibiotics
- U sensitive for UTI only (non systemic infection)
- X1 no data
- X2 active in vitro, but not used clinically
- X3 active in vitro, but not clinically effective for Group A strep pharyngitis or infections due to E. faecalis
- X4 active in vitro, but not clinically effective for strep pneumonia
See Also
References
- ↑ Sanford Guide to Antimicrobial Therapy 2014
