clarithromycin
(klar ith' ro my sin)
Biaxin, Biaxin XL
Pregnancy Category C
Drug class
Macrolide antibiotic
Therapeutic actions
Inhibits protein synthesis in susceptible bacteria, causing cell death.
Indications
· Treatment of URIs caused by Streptococcus pyogenes, S. pneumoniae
· Treatment of lower respiratory infections caused by Mycoplasma pneumoniae, S. pneumoniae, Haemophilus influenzae, Moraxella catarrhalis
· Treatment of skin and skin-structure infections caused by Staphylococcus aureus, S. pyogenes
· Treatment of disseminated mycobacterial infections due to Myobacterium avium and M. intracellular
· Treatment of active duodenal ulcer associated with Helicobacter pylori in combination with proton pump inhibitor
· Treatment of acute otitis media, acute maxillary sinusitis due to H. influenzae, M. cararrhalis, S. pneumoniae
· Treatment of mild to moderate community-acquired pneumonia in adults
Contraindications and cautions
· Contraindicated with hypersensitivity to clarithromycin, erythromycin, or any macrolide antibiotic.
· Use cautiously with colitis, hepatic or renal impairment, pregnancy, lactation.
Available forms
Tablets—250, 500 mg; granules for suspension—125, 250 mg/5 mL; ER tablets–500 mg
Dosages
ADULTS
· Pharyngitis, tonsillitis; pneumonia due to S. pneumoniae, M. pneumoniae; skin or skin-structure infections; lower respiratory infections due to S. pneumoniae, M. catarrhalis: 250 mg PO q 12 hr for 7–14 days.
· Acute maxillary sinusitis, lower respiratory infections caused by H. influenzae: 500 mg PO q 12 hr for 7–14 days.
· Mycobacterial infections: 500 mg PO bid.
· Treatment of duodenal ulcers: 500 mg PO tid plus omeprazole 40 mg PO q AM for 14 days, then omeprazole 20 mg PO q morning for 14 days.
· Treatment of community-acquired pneumonia: 250 mg PO q 12 hr for 7–14 days or 1,000 mg PO of ER tablet q 24 hr for 7 days.
PEDIATRIC PATIENTS
Usual dosage, 15 mg/kg/day PO q 12 hr for 10 days.
· Mycobacterial infections: 7.5 mg/kg PO bid.
GERIATRIC PATIENTS OR PATIENTS WITH IMPAIRED RENAL FUNCTION
Decrease dosage or prolong dosing intervals as appropriate.
Pharmacokinetics
Route | Onset | Peak |
Oral | Varies | 2 hr |
Metabolism: Hepatic; T1/2: 3–7 hr
Distribution: Crosses placenta; enters breast milk
Excretion: Urine
Adverse effects
· CNS: Dizziness, headache, vertigo, somnolence, fatigue
· GI: Diarrhea, abdominal pain, nausea, dyspepsia, flatulence, vomiting, melena, pseudomembranous colitis
· Other: Superinfections, increased PT, decreased WBC
Interactions
Drug-drug
· Increased serum levels and effects of carbamazepine, theophylline, lovastatin, phenytoin
Drug-food
· Food decreases the rate of absorption of clarithromycin but does not alter effectiveness
· Decreased metabolism and risk of toxic effects if combined with grapefruit juice; avoid this combination.
Nursing considerations
Assessment
· History: Hypersensitivity to clarithromycin, erythromycin, or any macrolide antibiotic; pseudomembranous colitis, hepatic or renal impairment, lactation, pregnancy
· Physical: Site of infection; skin color, lesions; orientation, GI output, bowel sounds, liver evaluation; culture and sensitivity tests of infection, urinalysis, LFTs, renal function tests
Interventions
· Culture infection before therapy.
· Do not cut or crush, and ensure that patient does not chew ER tablets.
· Monitor patient for anticipated response.
· Administer without regard to meals; administer with food if GI effects occur.
Teaching points
· Take drug with food if GI effects occur. Take the full course of therapy. Do not drink grapefruit juice while taking this drug.
· Shake suspension before use; do not refrigerate; do not cut, crush, or chew extended-release tablets; swallow them whole.
· You may experience these side effects: Stomach cramping, discomfort, diarrhea; fatigue, headache (medication may be ordered); additional infections in the mouth or vagina (consult with care provider for treatment).
· Report severe or watery diarrhea, severe nausea or vomiting, rash or itching, mouth sores, vaginal sores.
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