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cephalexin (Keflex, Panixine Disperdose)

 

Classes: Cephalosporins, 1st Generation

Dosing and uses of Keflex (cephalexin)

 

Adult dosage forms and strengths

capsule

  • 250mg
  • 500mg
  • 750mg

oral suspension

  • 125mg/5mL
  • 250mg/5mL

tablet

  • 250mg
  • 500mg

 

Genitourinary Tract Infections

250 mg PO q6hr; dosage range, 1-4 g/day in divided doses

 

Bone Infections

250 mg PO q6hr; dosage range, 1-4 g/day in divided doses

 

Uncomplicated Cystitis

250 mg PO q6hr or 500 mg PO q12hr; dosage range, 1-4 g/day in divided doses

 

Otitis Media

250 mg PO q6hr; dosage range, 1-4 g/day in divided doses

 

Skin/Skin Structure Infections

250 mg PO q6hr or 500 mg PO q12hr; dosage range, 1-4 g/day in divided doses

 

Respiratory Tract Infections

250 mg PO q6hr; dosage range, 1-4 g/day in divided doses

 

Streptococcal Pharyngitis

250 mg PO q6hr or 500 mg PO q12hr; dosage range, 1-4 g/day in divided doses

 

Cellulitis and Mastitis

500 mg PO q6hr; dosage range, 1-4 g/day in divided doses

 

Renal Impairment

CrCl <10 mL/min: 250-500 mg PO q12-24hr

CrCl 10-50 mL/min: 500 mg PO q8-12hr

 

Hepatic Impairment

Not studied

 

Dosing Considerations

Susceptible organisms

  • Gram-positive cocci, gram negative bacilli, gram-positive bacilli, gram-negative cocci, anaerobes

 

Pediatric dosage forms and strengths

capsule

  • 250mg
  • 500mg

oral suspension

  • 125mg/5mL
  • 250mg/5mL

tablet

  • 125mg
  • 250mg

 

Uncomplicated Cystitis

<15 years: 25-50 mg/kg/day PO divided q6-8hr for 10 days; not to exceed 4 g/day

>15 years: 250 mg PO q6hr; dosage range, 1-4 g/day in divided doses

 

Genitourinary Tract Infections

25-50 mg/kg/day PO divided q6-8hr for 10 days; not to exceed 4 g/day

 

Beta-Hemolytic Streptococcal Infections

25-50 mg/kg/day PO divided q6-8hr for 10 days; not to exceed 4 g/day

 

Bone Infections

25-50 mg/kg/day PO divided q6-8hr for 10 days; not to exceed 4 g/day

 

Otitis Media

75-100 mg/kg/day PO divided q6hr for 10 days; not to exceed 4 g/day

 

Skin/Skin Structure Infections

25-50 mg/kg/day PO divided q6-8hr for 10 days; not to exceed 4 g/day

 

Respiratory Tract Infections

25-50 mg/kg/day PO divided q6-8hr for 10 days; not to exceed 4 g/day

 

Streptococcal Pharyngitis

25-50 mg/kg PO q12hr for 10 days; not to exceed 500 mg q12hr

 

Cellulitis and Mastitis

Adolescents: 500 mg PO q6hr; dosage range, 1-4 g/day in divided doses

 

Keflex (cephalexin) adverse (side) effects

Frequency not defined

Abdominal pain

Agitation

Anemia

Angioedema

Confusion

Diarrhea

Dizziness

Dyspepsia

Elevated transaminases

Eosinophilia hemolytic

Epidermal necrolysis

Erythema multiform

Fatigue

Gastritis

Genital pruritus

Hallucinations

Headache

Hemolytic anemia

Hypersensitivity

Nephritis

Neutropenia

Pseudomembranous colitis

Thrombocytopenia

Transient hepatitis

Toxic epidermal necrolysis

Urticaria

Vaginal discharge

Vomiting

 

Warnings

Contraindications

Documented hypersensitivity

 

Cautions

Endocarditis prophylaxis is appropriate only for high-risk patients, per American Heart Association guidelines

Adjust dose in severe renal insufficiency (high doses may cause CNS toxicity)

Superinfections and promotion of nonsusceptible organisms may occur with prolonged use or repeated therapy

Prolonged treatment, hepatic or renal disease, or nutritional deficiency may be associated with increased international normalized ratio (INR)

Prolonged use is associated with fungal or bacterial superinfection

Use with caution in patients with history of hypersensitivity to penicillin

 

Pregnancy and lactation

Pregnancy category: B

Lactation: Drug excreted in breast milk; use with caution

 

Pregnancy categories

A: Generally acceptable. Controlled studies in pregnant women show no evidence of fetal risk.

B: May be acceptable. Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk.

C: Use with caution if benefits outweigh risks. Animal studies show risk and human studies not available or neither animal nor human studies done.

D: Use in LIFE-THREATENING emergencies when no safer drug available. Positive evidence of human fetal risk.

X: Do not use in pregnancy. Risks involved outweigh potential benefits. Safer alternatives exist.

NA: Information not available.

 

Pharmacology of Keflex (cephalexin)

Mechanism of action

Binds to one or more of the penicillin binding proteins, which in turn inhibits synthesis of bacterial cell walL

 

Absorption

Bioavailability: 90%; absorption delayed in young children

Peak serum time: 1 hr

Peak plasma concentration: 10-18 mcg/mL (500-mg dose)

 

Distribution

Distributed widely into most tissues and fluids; penetrates CSF poorly

Protein bound: 6-15%

 

Metabolism

Minimally metabolized in liver

 

Elimination

Half-life: 0.5-1.2 hr

Excretion: Urine (80-100% as unchanged drug)