What is the recommended dose of clarithromycin (Biaxin) for adults?

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Clarithromycin Dosing for Adults

For most adult infections, clarithromycin should be dosed at 500 mg twice daily for 7-14 days depending on the indication, or alternatively 1000 mg once daily using the extended-release formulation. 1, 2, 3

Standard Adult Dosing by Indication

Respiratory Tract Infections

  • Community-acquired pneumonia: 500 mg twice daily for 7-14 days (immediate-release) OR 1000 mg once daily for 7 days (extended-release) 4, 3
  • Acute bacterial exacerbation of chronic bronchitis: 500 mg twice daily for 7 days (immediate-release) OR 1000 mg once daily for 7 days (extended-release) 3
  • Acute maxillary sinusitis: 500 mg twice daily for 14 days (immediate-release) OR 1000 mg once daily for 14 days (extended-release) 3
  • Group A streptococcal pharyngitis: 250 mg twice daily for 10 days 4

Mycobacterial Infections

  • Mycobacterium avium complex (MAC) treatment: 500 mg twice daily in combination with ethambutol 15 mg/kg daily 1
  • MAC prophylaxis in AIDS (CD4 <50 cells/μL): 500 mg twice daily 1
  • Pertussis: 500 mg twice daily for 7 days 1

Critical Dosing Considerations

Renal Impairment

  • Severe renal impairment (CrCl <30 mL/min): Reduce dose by 50% 2, 3
  • Moderate renal impairment (CrCl 30-60 mL/min) with concomitant ritonavir or atazanavir: Reduce dose by 50% 4, 3
  • Severe renal impairment (CrCl <30 mL/min) with concomitant ritonavir or atazanavir: Reduce dose by 75% 4, 3

Special Populations

  • Elderly patients (>70 years) or low body weight (<50 kg): Consider reducing to 250 mg twice daily due to increased risk of gastrointestinal intolerance 1
  • No dosage adjustment required for hepatic impairment alone 5

Administration Guidelines

Extended-Release Formulation

  • Must be taken with food to maximize bioavailability (30% reduction in absorption when taken fasting) 3, 6
  • Swallow tablets whole—do not chew, break, or crush 3
  • Extended-release provides equivalent bioavailability to immediate-release with lower peak concentrations and reduced gastrointestinal side effects 6

Immediate-Release Formulation

  • Can be taken with or without food 7
  • Absorption is unaffected by food 7

Drug Interaction Adjustments

HIV Antiretrovirals

  • With ritonavir or lopinavir-ritonavir: Reduce clarithromycin dose by 50% if CrCl <60 mL/min; reduce by 75% if CrCl <30 mL/min 4, 2
  • With efavirenz: Clarithromycin AUC decreases by 39%; efficacy may be uncertain, monitor closely for treatment failure 4, 2
  • With nevirapine: Clarithromycin AUC decreases by 35%; monitor closely for treatment failure 4

Contraindicated Combinations

  • Absolutely contraindicated with cisapride, pimozide, astemizole, or terfenadine due to risk of fatal cardiac arrhythmias (torsades de pointes) 2, 3
  • Contraindicated with colchicine in patients with renal or hepatic impairment 3
  • Contraindicated with lomitapide, lovastatin, or simvastatin due to risk of rhabdomyolysis 3

Common Pitfalls to Avoid

Adverse Effects

  • Gastrointestinal symptoms (metallic taste, nausea, vomiting, diarrhea) are dose-related and most common 1, 6
  • Doses >1000 mg/day are poorly tolerated in most adults and should be avoided 1
  • Extended-release formulation has significantly less severe gastrointestinal adverse events compared to immediate-release (P = 0.018) 6

Resistance Considerations

  • Macrolide resistance in Streptococcus pneumoniae and Staphylococcus aureus is well-documented and varies geographically 4, 3
  • Use 500 mg twice daily (not 250 mg twice daily) when treating H. pylori to minimize resistance development 8
  • Susceptibility testing should be performed when clinically indicated 3

CYP3A4 Interactions

  • Clarithromycin is a potent CYP3A4 inhibitor and can increase levels of carbamazepine, cyclosporine, digoxin, theophylline, warfarin, and midazolam 2, 5
  • Monitor closely and adjust doses of these medications as needed 5

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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