Pharm
Ciprofloxacin
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Ciprofloxacin
, Cipro
See Also
Ofloxacin
Fluoroquinolone
Second Generation Fluoroquinolone
Indications
See
Second Generation Fluoroquinolone
Complicated
Urinary Tract Infection
s
Specific types of
Bacteria
l
Gastroenteritis
Prostatitis
Sexually Transmitted Disease
Avoid in
Community Acquired Pneumonia
Risk of pneumococcal bacteremia and
Meningitis
Additional Indications specific to Ciprofloxacin (not with
Ofloxacin
)
Pseudomonas
aeruginosa
Bacillus anthracis
or
Anthrax
(first line agent)
Vibrio Cholerae
(
Norfloxacin
also covers)
Yersinia pestis
or
Plague
(first line agent)
Tularemia
(alternative medication)
Contraindications
See
Fluoroquinolone
Myasthenia Gravis
(exacerbates motor weakness)
Tizanidine
use
Children
Relative contraindication due to risk of
Arthropathy
in animals
Studies have not demonstrated
Arthropathy
(other than transient large joint
Arthralgia
s)
Ciprofloxacin is commonly used off label in children with
Cystic Fibrosis
(due to
Pseudomonas
coverage)
Mechanism
See
Fluoroquinolone
Medications
Tablets: 250, 500 and 750 mg
Oral Suspension 250 and 500 mg per 5 ml
Shake container well for 15 seconds before administering dose
Do not give via nasogastric or
Feeding Tube
Extended release tablets: 500 and 1000 mg
Not interchangeable with regular, non-extended release formulations
Dosing
Adult
See
Anthrax
Urinary Tract Infection
Use higher dose of range for
Pyelonephritis
for 7 to 14 days
Give 200 to 400 mg IV every 12 hours OR
Take 250 to 500 mg orally twice daily OR
Extended Release Ciprofloxacin 1000 mg orally daily
Chronic Bacterial Prostatitis
Take 500 mg orally twice daily for up to 28 days
Diverticulitis
or Complicated intraabdominal infections (with
Metronidazole
)
Give 400 mg IV every 12 hours OR
Take 500 mg orally twice daily
Infectious Diarrhea
Take 500 mg orally twice daily for 5 to 7 days
Use 1 to 3 days (or 750 mg for one dose) for
Traveler's Diarrhea
Use 10 days for
Typhoid Fever
Malignant Otitis Externa
(not FDA approved)
Give 400 mg IV every 12 hours, or
Take 750 mg orally every 12 hours
Foot
Osteomyelitis
due to
Pseudomonas Osteochondritis
(
Sweaty Tennis Shoe Syndrome
)
Take 750 mg orally twice daily for up to 6 to 8 weeks
Bone and joint infections (based on sensitivity testing, treated for 4 to 8 weeks)
Give 400 mg IV every 8 to 12 hours initially, then
Take 500 to 750 mg orally twice daily
Plague
(treated for 14 days)
Give 400 mg IV every 8 to 12 hours OR
Take 500 mg orally twice daily
Chancroid
(not FDA approved)
Take 500 mg orally twice daily for 3 days
Renal Dosing
(immediate release)
eGFR 30 to 50 ml/min: 250 to 500 mg orally every 12 hours
eGFR 5 to 29 ml/min: 200 to 400 mg IV every 18 to 24 hours OR 250 to 500 mg every 18 hours
Hemodialysis
: 250 to 500 mg orally every 24 hours after
Dialysis
Dosing
Child
See
Anthrax
See Precautions above under contraindications
Complicated
Urinary Tract Infection
or
Pyelonephritis
(age 1 to 17 years)
Give 6 to 10 mg/kg IV (up to 400 mg/dose) every 8 hours, then
Give 10 to 20 mg/kg (up to 750 mg/dose) orally every 12 hours
Plague
(age birth to 17 years, treated for 10 to 21 days)
Give 10 mg/kg IV (up to 400 mg/dose) every 8 to 12 hours, then
Give 15 mg/kg (up to 500 mg/dose) orally every 8 to 12 hours
Acute respiratory exacerbation of
Cystic Fibrosis
Give 10 mg/kg IV (up to 400 mg/dose) every 8 to 12 hours for 7 days, then
Give 20 mg/kg (up to 750 mg/dose) orally every 12 hours for a total course of 10 to 21 days
Adverse Effects
See
Fluoroquinolone
Fluoroquinolone
s have several serious warnings (e.g. tendon rupture,
Neuropathy
,
Aortic Dissection
)
QTc Prolongation
Hypersensitivity
Urine Crystal
formation (in alkaline urine)
Photosensitivity (
Sunburn
risk)
Gastrointestinal (
Nausea
,
Vomiting
,
Diarrhea
,
Abdominal Pain
)
Neurologic (
Headache
,
Dizziness
, confusion)
Rash
Serum transaminase increase
Serum Creatinine
increase
White cell changes (
Eosinophilia
,
Neutropenia
)
Seizure
risk (class effect due to
GABA
inhibition)
Safety
Avoided in pregnancy (despite pregnancy Category C)
Cartilage damage risk
Considered safe in
Lactation
However, risk of pediatric
Arthropathy
Pharmacokinetics
Rapid but variable absorption, reaching peak levels within 1 to 2 hours of ingestion
Half-Life
: 4 hours
Partial hepatic metabolism and renal excretion
Urine concentrations remain high for many hours after dose
Distributes widely (except CSF), with high concentrations in urine, stool, bile,
Prostate
, bone and
Sputum
Drug Interactions
Sulfonylurea
s
Hypoglycemia
risk
Warfarin
May potentiate
Anticoagulant
effects
Tizanidine
Do not use with Ciprofloxacin
Ciprofloxacin is a strong
CYP1A2 Inhibitor
and increases drug levels of its substrates
Olanzapine
Ropinirole
Zolpidem
Drugs that interfere with absorption (give at least 2 hours before or after dose)
Antacid
s containing
Calcium
, aluminum or
Magnesium
Sucralfate
Iron
Zinc
Yogurt, milk or
Calcium
fortified juice (but may take with dairy containing meals)
Resources
Ciprofloxacin Tablet (DailyMed)
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3e4402d4-e0d3-9846-3e81-ed46f34137fe
Ciprofloxacin Injection Solution (DailyMed)
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e82f52f2-ecf8-4c04-a206-f3253b265903
References
(1988) Med Lett Drugs Ther 30(758): 11-3
King (2000) Am Fam Physician 61(9):2741-8 [PubMed]
O'Donnell (2000) Infect Dis Clin North Am 14(2):489-513 [PubMed]
Oliphant (2002) Am Fam Physician 65(3):455-64 [PubMed]
Owens (2000) Med Clin North Am 84(6):1447-69 [PubMed]
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