Clarithromycin: Difference between revisions
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==General== | ==General== | ||
*Type: | *Type: [[Is DrugClass::Macrolide]] | ||
*Dosage Forms: | *Dosage Forms: 250, 500, 500ER; 125, 250/5ml | ||
*Common Trade Names: | *Common Trade Names: Biaxin, Biaxin XL | ||
==Adult Dosing== | ==Adult Dosing== | ||
===Infections, bacterial=== | |||
*250-500mg PO q12h x 7-14d | |||
*Alt: 1000mg ER PO QD x 7-14d | |||
===Indications by Disease=== | |||
{{#ask: [[Has DrugName::Clarithromycin]] [[Has Population::Adult]] | |||
|?Treats disease=Disease | |||
|?Has Dose=Dose | |||
|?Has Context=Context | |||
|format=table | |||
|limit=50 | |||
|mainlabel=- | |||
|headers=show | |||
|sort=Treats disease | |||
}} | |||
==Pediatric Dosing== | ==Pediatric Dosing== | ||
===Infections, bacteria=== | |||
*> 6 months: 15mg/kg/day PO divided q12h, max 1000mg/day | |||
===Indications by Disease=== | |||
{{#ask: [[Has DrugName::Clarithromycin]] [[Has Population::Pediatric]] | |||
|?Treats disease=Disease | |||
|?Has Dose=Dose | |||
|?Has Context=Context | |||
|format=table | |||
|limit=50 | |||
|mainlabel=- | |||
|headers=show | |||
|sort=Treats disease | |||
}} | |||
==Special Populations== | ==Special Populations== | ||
*Pregnancy: | *Pregnancy: C (risk cannot be ruled out) | ||
*Lactation: | *Lactation: safety unknown | ||
*Renal Dosing | *Renal Dosing | ||
**Adult | **Adult | ||
***all uses with out ritonavir or atazanavir | |||
****GFR < 30: decrease dose 50% or give IR form q24h or ER form q48h | |||
****HD/PD: no supplement | |||
***concomitant ritonavir or atazanavir | |||
****GFR 30-60: decrease dose 50% | |||
****GFR < 30: decrease dose 75% | |||
****HD/PD: no supplement | |||
**Pediatric | **Pediatric | ||
***all uses without ritonavir or atazanavir | |||
****GFR < 30: decrease dose 50% or give q24h | |||
****HD/PD: no supplement | |||
***concomitant ritonavir or atazanavir | |||
****not defined | |||
*Hepatic Dosing | *Hepatic Dosing | ||
**Adult | **Adult: no adjustment | ||
**Pediatric | **Pediatric: no adjustment | ||
==Contraindications== | ==Contraindications== | ||
*Allergy to class/drug | *Allergy to class/drug | ||
*Liver disease | |||
*Renal disease | |||
*prolonged QT | |||
*ventricular arrythmias or history of | |||
*history of torsades de pointes | |||
*uncorrected electrolyte abnormalities | |||
*significant bradycardia | |||
*caution if recent MI | |||
*caution if CHF | |||
*caution in female and elderly | |||
*caution in myasthenia gravis | |||
*caution with digoxin co-administration | |||
==Adverse Reactions== | ==Adverse Reactions== | ||
===Serious=== | ===Serious=== | ||
*superinfection | |||
*C-difficile-associated diarrhea | |||
*hepatotoxicity | |||
*interstitial nephritis | |||
*pancreatitis | |||
*QT prolongation | |||
*ventricular arrhythmias | |||
*torsades de pointes | |||
*thrombocytopenia | |||
*leukopenia | |||
*neutropenia | |||
*hearing loss, reversible | |||
*seizures | |||
*behavioral disturbances | |||
*psychosis | |||
*hallucinations | |||
*psychiatric disturbance | |||
*anaphylaxis | |||
*erythema multiforme | |||
*Stevens-Johnson Syndrome | |||
*drug rash with eosinophilia and systemic sx | |||
*myasthenia gravis exacerbation | |||
*rhabdomyolysis | |||
===Common=== | ===Common=== | ||
*diarrhea | |||
*nausea and vomiting | |||
*taste changes | |||
*abdominal pain | |||
*dyspepsia | |||
*headache | |||
*rash | |||
==Pharmacology== | ==Pharmacology== | ||
*Half-life: | *Half-life: 3-4 hours (increased with dosage increase)<ref>Ferrero JL, Bopp BA, Marsh KC, et al. Metabolism and Disposition of Clarithromycin in Man. Drug Metab Dispos. 1990;18(4):441–446. [PubMed 1976065]</ref> | ||
*Metabolism: | *Metabolism: hepatic (rapid first-pass metabolism), CYP3A4 | ||
*Excretion: | *Excretion: renal | ||
*Mechanism of Action: | *Mechanism of Action: interferes with bacterial protein synthesis by binding to a component of the 50S subunit | ||
==[[Antibiotic Sensitivities]]<ref>Sanford Guide to Antimicrobial Therapy 2014</ref>== | |||
{| class="wikitable" | |||
| align="center" style="background:#f0f0f0;"|'''Group''' | |||
| align="center" style="background:#f0f0f0;"|'''Organism''' | |||
| align="center" style="background:#f0f0f0;"|'''Sensitivity''' | |||
|- | |||
| Gram Positive||[[Strep. Group A, B, C, G]]||I | |||
|- | |||
| ||[[Strep. Pneumoniae]]||I | |||
|- | |||
| ||[[Viridans strep]]||X1 | |||
|- | |||
| ||Strep. anginosus gp||X1 | |||
|- | |||
| ||[[Enterococcus faecalis]]||R | |||
|- | |||
| ||[[Enterococcus faecium]]||R | |||
|- | |||
| ||[[MSSA]]||'''S''' | |||
|- | |||
| ||[[MRSA]]||R | |||
|- | |||
| ||[[CA-MRSA]]||I | |||
|- | |||
| ||[[Staph. Epidermidis]]||R | |||
|- | |||
| ||[[C. jeikeium]]||R | |||
|- | |||
| ||[[L. monocytogenes]]||'''S''' | |||
|- | |||
| Gram Negatives||[[N. gonorrhoeae]]||I | |||
|- | |||
| ||[[N. meningitidis]]||X1 | |||
|- | |||
| ||[[Moraxella catarrhalis]]||'''S''' | |||
|- | |||
| ||[[H. influenzae]]||'''S''' | |||
|- | |||
| ||[[E. coli]]||R | |||
|- | |||
| ||[[Klebsiella]] sp||R | |||
|- | |||
| ||E. coli/Klebsiella ESBL+||R | |||
|- | |||
| ||E coli/Klebsiella KPC+||R | |||
|- | |||
| ||[[Enterobacter]] sp, AmpC neg||R | |||
|- | |||
| ||[[Enterobacter]] sp, AmpC pos||R | |||
|- | |||
| ||[[Serratia]] sp||X1 | |||
|- | |||
| ||Serratia marcescens||R | |||
|- | |||
| ||[[Salmonella]] sp||R | |||
|- | |||
| ||[[Shigella]] sp||R | |||
|- | |||
| ||[[Proteus mirabilis]]||X1 | |||
|- | |||
| ||[[Proteus vulgaris]]||R | |||
|- | |||
| ||[[Providencia sp.]]||X1 | |||
|- | |||
| ||[[Morganella sp.]]||X1 | |||
|- | |||
| ||[[Citrobacter freundii]]||X1 | |||
|- | |||
| ||[[Citrobacter diversus]]||X1 | |||
|- | |||
| ||[[Citrobacter sp.]]||X1 | |||
|- | |||
| ||[[Aeromonas sp]]||X1 | |||
|- | |||
| ||[[Acinetobacter sp.]]||R | |||
|- | |||
| ||[[Pseudomonas aeruginosa]]||R | |||
|- | |||
| ||[[Burkholderia cepacia]]||R | |||
|- | |||
| ||[[Stenotrophomonas maltophilia]]||R | |||
|- | |||
| ||[[Yersinia enterocolitica]]||R | |||
|- | |||
| ||[[Francisella tularensis]]||X1 | |||
|- | |||
| ||[[Brucella sp.]]||R | |||
|- | |||
| ||[[Legionella sp.]]||'''S''' | |||
|- | |||
| ||[[Pasteurella multocida]]||X1 | |||
|- | |||
| ||[[Haemophilus ducreyi]]||X1 | |||
|- | |||
| ||[[Vibrio vulnificus]]||X1 | |||
|- | |||
| Misc||[[Chlamydophila sp]]||'''S''' | |||
|- | |||
| ||[[Mycoplasm pneumoniae]]||'''S''' | |||
|- | |||
| ||[[Rickettsia sp]]||X1 | |||
|- | |||
| ||[[Mycobacterium avium]]||'''S''' | |||
|- | |||
| Anaerobes||[[Actinomyces]]||'''S''' | |||
|- | |||
| ||[[Bacteroides fragilis]]||R | |||
|- | |||
| ||[[Prevotella melaninogenica]]||'''S''' | |||
|- | |||
| ||[[Clostridium difficile]]||X1 | |||
|- | |||
| ||[[Clostridium (not difficile)]]||'''S''' | |||
|- | |||
| ||[[Fusobacterium necrophorum]]||R | |||
|- | |||
| ||[[Peptostreptococcus sp.]]||I | |||
|} | |||
===Key=== | |||
{{Template:Antibacterial Spectra Key}} | |||
==See Also== | ==See Also== | ||
*[[Antibiotics (Main)]] | *[[Antibiotics (Main)]] | ||
== | ==References== | ||
<references/> | <references/> | ||
[[Category: | [[Category:Pharmacology]] | ||
[[Category:ID]] | |||
Latest revision as of 11:07, 20 March 2026
General
- Type: Macrolide
- Dosage Forms: 250, 500, 500ER; 125, 250/5ml
- Common Trade Names: Biaxin, Biaxin XL
Adult Dosing
Infections, bacterial
- 250-500mg PO q12h x 7-14d
- Alt: 1000mg ER PO QD x 7-14d
Indications by Disease
| Disease | Dose | Context |
|---|---|---|
| COPD exacerbation | 1000mg ER PO q24 x 7d (with food, do not cut/crush/chew); Alt: 250-500mg PO q12h x 7-14d | Chronic bronchitis, acute bacterial exacerbation |
| Endocarditis | 500mg (15mg/kg) PO | Dental Procedure Prophylaxis |
| Helicobacter pylori | triple treatment: 500mg PO q12hr x 7-14d; dual treatment: 500mg PO q8h x 14d (give with Omeprazole 40mg QD x 14d) | H. pylori infection |
| Infectious tenosynovitis | 500mg PO twice daily | Mycobacteria |
| Mycobacterium avium complex | 500mg PO q12h | Primary prophylaxis |
| Mycobacterium avium complex | 500mg PO q12h (use with ethambutol) | Treatment, disseminated |
| Mycobacterium avium complex | 500mg PO q12h (use with ethambutol) | Secondary prophylaxis |
| Pertussis | 500mg BID x7 days | Adults |
| Pneumonia (main) | 500 mg BID or clarithromycin ER 1,000 mg daily | Outpatient, Healthy |
| Pneumonia (main) | 500 mg BID OR clarithromycin ER 1,000 mg daily | Outpatient, Unhealthy |
| Pneumonia (main) | 500 mg BID | Inpatient, CAP Non-ICU |
| Streptococcal pharyngitis | 7.5 mg/kg/dose PO BID (maximum = 250 mg/dose) x 10 days | Penicillin Allergy (anaphylaxis) |
Pediatric Dosing
Infections, bacteria
- > 6 months: 15mg/kg/day PO divided q12h, max 1000mg/day
Indications by Disease
| Disease | Dose | Context |
|---|---|---|
| Acute otitis media | 7.5mg/kg PO BID x 10 days | Penicillin Allergy |
| Helicobacter pylori | 20mg/kg/day PO divided BID x 7-14d; max 1000mg/day | H. pylori infection |
| Mycobacterium avium complex | 20mo-12yrs: 15mg/kg/day PO divided q12h (max 500mg/dose); >13yrs: 500mg PO q12h | Primary prophylaxis, HIV |
| Mycobacterium avium complex | 20mo-12yrs: 15-30mg/kg/day PO divided q12h (max 500mg/dose, use with ethambutol); >13yrs: 500mg PO q12h (use with ethambutol) | Treatment, disseminated |
| Mycobacterium avium complex | 20mo-12yrs: 15mg/kg/day PO divided q12h (max 500mg/dose, use with ethambutol); >13yrs: 500mg PO q12h (use with ethambutol) | Secondary prophylaxis, HIV |
| Pertussis | >6 months: 7.5mg/kg PO BID x 7 days (max 500mg/dose) | >1 month old |
| Pharyngitis | >6mo: 15mg/kg/day PO divided q12h x 7-10d | Pharyngitis/tonsillitis, streptococcal |
| Streptococcal pharyngitis | 7.5mg/kg PO BID x 10 days (max 250mg/dose) | Pediatric PCN Allergy (severe) |
Special Populations
- Pregnancy: C (risk cannot be ruled out)
- Lactation: safety unknown
- Renal Dosing
- Adult
- all uses with out ritonavir or atazanavir
- GFR < 30: decrease dose 50% or give IR form q24h or ER form q48h
- HD/PD: no supplement
- concomitant ritonavir or atazanavir
- GFR 30-60: decrease dose 50%
- GFR < 30: decrease dose 75%
- HD/PD: no supplement
- all uses with out ritonavir or atazanavir
- Pediatric
- all uses without ritonavir or atazanavir
- GFR < 30: decrease dose 50% or give q24h
- HD/PD: no supplement
- concomitant ritonavir or atazanavir
- not defined
- all uses without ritonavir or atazanavir
- Adult
- Hepatic Dosing
- Adult: no adjustment
- Pediatric: no adjustment
Contraindications
- Allergy to class/drug
- Liver disease
- Renal disease
- prolonged QT
- ventricular arrythmias or history of
- history of torsades de pointes
- uncorrected electrolyte abnormalities
- significant bradycardia
- caution if recent MI
- caution if CHF
- caution in female and elderly
- caution in myasthenia gravis
- caution with digoxin co-administration
Adverse Reactions
Serious
- superinfection
- C-difficile-associated diarrhea
- hepatotoxicity
- interstitial nephritis
- pancreatitis
- QT prolongation
- ventricular arrhythmias
- torsades de pointes
- thrombocytopenia
- leukopenia
- neutropenia
- hearing loss, reversible
- seizures
- behavioral disturbances
- psychosis
- hallucinations
- psychiatric disturbance
- anaphylaxis
- erythema multiforme
- Stevens-Johnson Syndrome
- drug rash with eosinophilia and systemic sx
- myasthenia gravis exacerbation
- rhabdomyolysis
Common
- diarrhea
- nausea and vomiting
- taste changes
- abdominal pain
- dyspepsia
- headache
- rash
Pharmacology
- Half-life: 3-4 hours (increased with dosage increase)[1]
- Metabolism: hepatic (rapid first-pass metabolism), CYP3A4
- Excretion: renal
- Mechanism of Action: interferes with bacterial protein synthesis by binding to a component of the 50S subunit
Antibiotic Sensitivities[2]
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
