Ciprofloxacin: Difference between revisions
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===General=== | ===General=== | ||
*'''PO''' | *'''PO''' | ||
**20- | **20-30mg/kg/day PO divided q12h | ||
**First Dose: 10-15mg/kg PO x 1 | **First Dose: 10-15mg/kg PO x 1 | ||
**Max: | **Max: 750mg/dose PO | ||
*'''IV''' | *'''IV''' | ||
**15- | **15-30mg/kg/day IV divided q8-12h | ||
**First Dose: 5-15mg/kg IV x 1 | **First Dose: 5-15mg/kg IV x 1 | ||
**Max: | **Max: 400mg/dose IV | ||
===[[Anthrax]]=== | ===[[Anthrax]]=== | ||
| Line 64: | Line 64: | ||
*'''Inhalational, GI, Oropharyngeal''' | *'''Inhalational, GI, Oropharyngeal''' | ||
**20- | **20-30mg/kg/day IV/PO divided q12h x 60 days | ||
**First Dose: 10-15mg/kg IV x 1 (give with 1-2 additional antibiotics) | **First Dose: 10-15mg/kg IV x 1 (give with 1-2 additional antibiotics) | ||
*'''Cutaneous''' | *'''Cutaneous''' | ||
**20- | **20-30mg/kg/day IV/PO divided q12h x 7-10 days | ||
**First Dose: 10-15mg/kg IV/PO x 1 | **First Dose: 10-15mg/kg IV/PO x 1 | ||
***Info: Give x 60 days if [[bioterrorism]] suspected | ***Info: Give x 60 days if [[bioterrorism]] suspected | ||
*'''Post-Exposure Prophylaxis''' | *'''Post-Exposure Prophylaxis''' | ||
**20- | **20-30mg/kg/day PO divided q12h x 60 days (or exposure excluded) | ||
**First Dose: 10-15mg/kg PO x 1 | **First Dose: 10-15mg/kg PO x 1 | ||
| Line 77: | Line 77: | ||
''Not first line given adverse effects'' | ''Not first line given adverse effects'' | ||
*'''IV''' | *'''IV''' | ||
**6- | **6-10mg/kg IV q8h | ||
**First Dose: | **First Dose: | ||
**Max: | **Max: 400mg/dose IV | ||
*'''PO''' | *'''PO''' | ||
**10- | **10-20mg/kg PO q12h | ||
**First Dose: | **First Dose: | ||
**Max: | **Max: 750mg/dose PO | ||
==Special Populations== | ==Special Populations== | ||
Revision as of 22:49, 18 July 2016
General
- Type: Fluoroquinolones
- Dosage Forms: IV; PO (Standard: 100, 250, 500; ER 500, 1000)
- Common Trade Names: Cipro
Adult Dosing
General
- PO
- 250-750mg PO q12h
- First Dose: 250-750mg PO x1
- IV
- 200-400mg IV q12
- First Dose: 400mg IV x 1
- Alt: 400mg IV q8h
UTI
- Uncomplicated
- 500mg ER PO q24h x 3 days
- Alt: 250mg PO q12h x 3 days
- Complicated
- IV: 400mg IV q12h x 7-14 days
- PO: 1000mg ER PO q24h x 7-14 days
- Alt: 500mg PO q12h x 7-14 days
Anthrax
- Inhalational, GI, Oropharyngeal
- 400mg IV q12h OR 500mg PO q12 x 60 days
- First dose: 400mg IV + 1-2 additional antibiotics
- Cutaneous
- 400mg IV q12h OR 500mg PO q12 x 7-10 days
- Info: Give x 60 days if bioterrorism suspected
- 400mg IV q12h OR 500mg PO q12 x 7-10 days
- Post-Exposure Prophylaxis
- 500mg PO q12h x 60 days (or exposure excluded)
Traveler's Diarrhea[1]
- 750mg PO BID x 1-3 days
Typhoid Fever
- 500mg PO q12h x 2 weeks
Chancroid
- 500mg PO q12h x 3 days
Salmonella
- Acute
- 500-750mg PO q12h x 3-7 days
- Extend treatment x 1 week if immunocompromised
- 500-750mg PO q12h x 3-7 days
- Chronic Carrier
- 750mg PO q12h x 1 month
Pediatric Dosing
General
- PO
- 20-30mg/kg/day PO divided q12h
- First Dose: 10-15mg/kg PO x 1
- Max: 750mg/dose PO
- IV
- 15-30mg/kg/day IV divided q8-12h
- First Dose: 5-15mg/kg IV x 1
- Max: 400mg/dose IV
Anthrax
Max (All): 400mg/dose IV or 500mg/dose PO
- Inhalational, GI, Oropharyngeal
- 20-30mg/kg/day IV/PO divided q12h x 60 days
- First Dose: 10-15mg/kg IV x 1 (give with 1-2 additional antibiotics)
- Cutaneous
- 20-30mg/kg/day IV/PO divided q12h x 7-10 days
- First Dose: 10-15mg/kg IV/PO x 1
- Info: Give x 60 days if bioterrorism suspected
- Post-Exposure Prophylaxis
- 20-30mg/kg/day PO divided q12h x 60 days (or exposure excluded)
- First Dose: 10-15mg/kg PO x 1
UTI, Complicated (1-17 Years Old)
Not first line given adverse effects
- IV
- 6-10mg/kg IV q8h
- First Dose:
- Max: 400mg/dose IV
- PO
- 10-20mg/kg PO q12h
- First Dose:
- Max: 750mg/dose PO
Special Populations
- Drug ratings in pregnancy: C (but indicated for anthrax)
- Lactation risk categories: Probably safe
- Renal Dosing
- Adult: renal impairment less than Cr clearance 30 mL/min, q24hrs instead of q12hrs
- Pediatric
- Hepatic Dosing - no dose adjustments needed
Contraindications
- Allergy to class/drug
- Administration with Tizanidine
Adverse Reactions
Serious
- Prolonged QT interval and Syncope/Torsades de pointes
- Photosensitivity
- Stevens-Johnson syndrome/Toxic epidermal necrolysis
- Clostridium difficile diarrhea, Pseudomembranous enterocolitis
- Rupture of tendon or Tendinitis
Common
Common
- Rash
- Diarrhea/Nausea/Vomiting
Pharmacology
- Half-life:
- Metabolism:
- Excretion:
- Mechanism of Action:
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
See Also
Source
- Micromedex
