Azithromycin: Difference between revisions
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==General== | ==General== | ||
*Type: | *Type: [[Is DrugClass::Macrolide]] | ||
*Dosage Forms: | *Dosage Forms: powder for solution, suspension reconstituted, packet, tablet | ||
*Common Trade Names: | *Dosage Strengths: powder for solution: 500mg, 2.5g; suspension reconstituted: 100, 200mg/5mL; packet: 1g; tablet: 250, 500, 600mg | ||
*Routes of Administration: PO, IV | |||
*Common Trade Names: Zithromax, Z-Pak, Zmax | |||
==Adult Dosing== | ==Adult Dosing== | ||
===[[Babesiosis]]=== | |||
''In combination with Atovaquone'' | |||
*Mild/Moderate: 500mg PO x1 on day 1, then 250mg PO q24h x7-10 days | |||
*Severe 500mg IV q24hr for 7 to 10 days] | |||
===Bacterial Infections=== | |||
*500mg PO x1 on day 1, then 250mg PO q24h x4 days | |||
===[[Strep Pharyngitis]]/tonsillitis=== | |||
*500mg PO x1 on day 1, then 250mg PO q24h x4 days] | |||
*Alt: 500mg PO q24h x3 days | |||
===[[COPD exacerbation]]=== | |||
*500mg PO x1 on day 1, then 250mg PO q24h x4 days | |||
*Alt: 500mg PO q24h x3 days | |||
===Community-acquired [[pneumonia]]=== | |||
*500mg PO x1 on day 1, then 250mg PO q24h x4 days | |||
*Alt: 500mg IV q24h x2 or more days, then 500mg PO q24h to complete 7-10 day course | |||
===[[Chlamydia]] (uncomplicated urethritis, cervicitis, oropharygeal)=== | |||
*1 g PO x1 | |||
===[[Gonorrhea]]=== | |||
*Initial or recurrent: 1 g PO x1 | |||
*Persistent: 2 g PO x1 | |||
===[[PID]]=== | |||
*500mg IV q24h x1-2 days, then 250mg PO q24h x5-6 days | |||
===[[Urethritis]], non-gonococcal initial infection=== | |||
*1 g PO x1 | |||
===[[Chancroid]]=== | |||
*1 g PO x1 | |||
===MAC=== | |||
*Disseminated: 500-600mg PO q24h (not 1st-line agent; use with ethambutol) | |||
*Primary prophylaxis: 1200mg PO qwk Alt: 600mg PO 2x/wk | |||
*Secondary prophylaxis: 500-600mg PO q24h (not 1st-line agent; use with ethambutol) | |||
===[[Endocarditis]] prophylaxis (dental)=== | |||
*500mg PO x1 (Start: 30-60min before procedure) | |||
===Pertussis=== | |||
*500mg PO on day 1, followed by 250mg q24hr for days 2-5 | |||
===Presumptive [[cervicitis]]=== | |||
*1 g PO x1 | |||
===[[Salmonella]]=== | |||
*1 g PO q24h x1 day, then 500mg PO q24h x2-6 days | |||
===[[Typhoid fever]]=== | |||
*10mg/kg PO q24h x1wk | |||
==Pediatric Dosing== | ==Pediatric Dosing== | ||
===[[Pneumonia (peds)]]=== | |||
*10mg/kg/day PO in a once daily dose on day 1 (max 500mg) | |||
**Followed by 5mg/kg/day PO once daily on days 2-5 | |||
===Bacterial sinusitis=== | |||
*Children ≥6 months: Oral: 10mg/kg PO once daily for 3 days (maximum: 500mg daily) | |||
===[[Otitis media]]=== | |||
*Children ≥6 months: | |||
**1-day regimen: 30mg/kg PO a single dose (maximum dose: 1,500mg) | |||
**3-day regimen: 10mg/kg PO once daily for 3 days (maximum: 500mg daily) | |||
**5-day regimen: 10mg/kg PO on day 1 (maximum: 500mg daily) followed by 5mg/kg/day once daily on days 2 to 5 (maximum: 250mg daily) | |||
===[[Pharyngitis]] (as an alternative agent in penicillin allergic patients)=== | |||
*Children ≥2 years and Adolescents: Oral: 12mg/kg/dose once daily for 5 days (maximum: 500mg daily) | |||
==Special Populations== | ==Special Populations== | ||
*Pregnancy: | *[[Drug Ratings in Pregnancy|Pregnancy Rating]]: B | ||
*Lactation: | *[[Lactation risk categories|Lactation risk]]: Excreted in low amounts of breast milk and may lead to rash, somnolence, and diarrhea in nursing infants | ||
*Renal Dosing | *Renal Dosing: Caution in patients with GFR <10 mL/minute, though primarily elimated through hepatic metabolism | ||
*Hepatic Dosing: Caution is indicated for potential hepatotoxicity though it is rare, and there are no specific dosage adjustments indicated for patients with liver failure | |||
*Hepatic Dosing | |||
==Contraindications== | ==Contraindications== | ||
* | *Hypersensitivity to azithromycin or other macrolides or any component of the formulation | ||
*History of cholestatic jaundice/hepatic dysfunction with prior Azithromycin use | |||
==Adverse Reactions== | ==Adverse Reactions== | ||
===Serious=== | ===Serious=== | ||
*[[Prolonged QT]] | |||
*[[Torsades]] | |||
*hepatic necrosis | |||
*Eaton-Lambert | |||
*[[Myasthenia gravis]] | |||
*Corneal erosion | |||
===Common=== | ===Common=== | ||
*[[Vomiting]] | |||
*[[Diarrhea]] | |||
*[[Abdominal pain]] | |||
*[[Headache]] | |||
*Vision changes | |||
==Pharmacology== | ==Pharmacology== | ||
*Half-life: | *Half-life: 68 hrs | ||
*Metabolism: | *Metabolism: Hepatic | ||
*Excretion: | *Excretion: Biliary | ||
*Mechanism of Action: | *Mechanism of Action:Binds 50S ribosomal subunit interfering with microbial protein synthesis | ||
==[[Antibiotic Sensitivities]]<ref>Sanford Guide to Antimicrobial Therapy 2014</ref>== | ==[[Antibiotic Sensitivities]]<ref>Sanford Guide to Antimicrobial Therapy 2014</ref>== | ||
| Line 157: | Line 237: | ||
*[[Antibiotics (Main)]] | *[[Antibiotics (Main)]] | ||
== | ==References== | ||
<references/> | |||
[[Category:Pharmacology]] [[Category:ID]] | |||
*Epocrates | |||
*Micromedex | |||
Latest revision as of 19:53, 28 January 2026
General
- Type: Macrolide
- Dosage Forms: powder for solution, suspension reconstituted, packet, tablet
- Dosage Strengths: powder for solution: 500mg, 2.5g; suspension reconstituted: 100, 200mg/5mL; packet: 1g; tablet: 250, 500, 600mg
- Routes of Administration: PO, IV
- Common Trade Names: Zithromax, Z-Pak, Zmax
Adult Dosing
Babesiosis
In combination with Atovaquone
- Mild/Moderate: 500mg PO x1 on day 1, then 250mg PO q24h x7-10 days
- Severe 500mg IV q24hr for 7 to 10 days]
Bacterial Infections
- 500mg PO x1 on day 1, then 250mg PO q24h x4 days
Strep Pharyngitis/tonsillitis
- 500mg PO x1 on day 1, then 250mg PO q24h x4 days]
- Alt: 500mg PO q24h x3 days
COPD exacerbation
- 500mg PO x1 on day 1, then 250mg PO q24h x4 days
- Alt: 500mg PO q24h x3 days
Community-acquired pneumonia
- 500mg PO x1 on day 1, then 250mg PO q24h x4 days
- Alt: 500mg IV q24h x2 or more days, then 500mg PO q24h to complete 7-10 day course
Chlamydia (uncomplicated urethritis, cervicitis, oropharygeal)
- 1 g PO x1
Gonorrhea
- Initial or recurrent: 1 g PO x1
- Persistent: 2 g PO x1
PID
- 500mg IV q24h x1-2 days, then 250mg PO q24h x5-6 days
Urethritis, non-gonococcal initial infection
- 1 g PO x1
Chancroid
- 1 g PO x1
MAC
- Disseminated: 500-600mg PO q24h (not 1st-line agent; use with ethambutol)
- Primary prophylaxis: 1200mg PO qwk Alt: 600mg PO 2x/wk
- Secondary prophylaxis: 500-600mg PO q24h (not 1st-line agent; use with ethambutol)
Endocarditis prophylaxis (dental)
- 500mg PO x1 (Start: 30-60min before procedure)
Pertussis
- 500mg PO on day 1, followed by 250mg q24hr for days 2-5
Presumptive cervicitis
- 1 g PO x1
Salmonella
- 1 g PO q24h x1 day, then 500mg PO q24h x2-6 days
Typhoid fever
- 10mg/kg PO q24h x1wk
Pediatric Dosing
Pneumonia (peds)
- 10mg/kg/day PO in a once daily dose on day 1 (max 500mg)
- Followed by 5mg/kg/day PO once daily on days 2-5
Bacterial sinusitis
- Children ≥6 months: Oral: 10mg/kg PO once daily for 3 days (maximum: 500mg daily)
Otitis media
- Children ≥6 months:
- 1-day regimen: 30mg/kg PO a single dose (maximum dose: 1,500mg)
- 3-day regimen: 10mg/kg PO once daily for 3 days (maximum: 500mg daily)
- 5-day regimen: 10mg/kg PO on day 1 (maximum: 500mg daily) followed by 5mg/kg/day once daily on days 2 to 5 (maximum: 250mg daily)
Pharyngitis (as an alternative agent in penicillin allergic patients)
- Children ≥2 years and Adolescents: Oral: 12mg/kg/dose once daily for 5 days (maximum: 500mg daily)
Special Populations
- Pregnancy Rating: B
- Lactation risk: Excreted in low amounts of breast milk and may lead to rash, somnolence, and diarrhea in nursing infants
- Renal Dosing: Caution in patients with GFR <10 mL/minute, though primarily elimated through hepatic metabolism
- Hepatic Dosing: Caution is indicated for potential hepatotoxicity though it is rare, and there are no specific dosage adjustments indicated for patients with liver failure
Contraindications
- Hypersensitivity to azithromycin or other macrolides or any component of the formulation
- History of cholestatic jaundice/hepatic dysfunction with prior Azithromycin use
Adverse Reactions
Serious
- Prolonged QT
- Torsades
- hepatic necrosis
- Eaton-Lambert
- Myasthenia gravis
- Corneal erosion
Common
- Vomiting
- Diarrhea
- Abdominal pain
- Headache
- Vision changes
Pharmacology
- Half-life: 68 hrs
- Metabolism: Hepatic
- Excretion: Biliary
- Mechanism of Action:Binds 50S ribosomal subunit interfering with microbial protein 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
- Epocrates
- Micromedex
