Indications |
Oral Susceptible infections Adult: 250 mg bid increased to 500 mg bid for severe infections if necessary for 7-14 days. Child: 7.5 mg/kg bid for 5-10 days.
Oral Respiratory tract infections Adult: 250 mg bid increased to 500 mg bid for severe infections if necessary for 7-14 days. Child: 7.5 mg/kg bid for 5-10 days.
Oral Skin and soft tissue infections Adult: 250 mg bid increased to 500 mg bid for severe infections if necessary for 7-14 days. Child: 7.5 mg/kg bid for 5-10 days.
Oral Mycobacterium avium complex infections Adult: 500 mg bid in combination with other antimycobacterials. Child: 7.5 mg/kg bid; to be used with other antimycobacterials. May increase dose to 15 mg/kg (max: 500 mg) bid.
Oral Leprosy Adult: 500 mg daily as part of an alternative multidrug therapy.
Oral Eradication of H. pylori associated with peptic ulcer disease Adult: 500 mg bid; given in combination with another antibacterial and either a proton pump inhibitor or H2-receptor antagonist for 7-14 days. Child: ≥1 yr: 7.5 mg/kg bid; may be given with another antibacterial and a proton pump inhibitor for 7 days.
Intravenous Respiratory tract infections Adult: 500 mg bid for 2-5 days. Dose to be infused over 60 minutes in a 0.2% solution; revert to oral therapy whenever possible. Child: 1 mth-12 yr: 7.5 mg/kg every 12 hr. Dose to be given via infusion into proximal vein.
Intravenous Skin and soft tissue infections Adult: 500 mg bid for 2-5 days. Dose to be infused over 60 minutes in a 0.2% solution; revert to oral therapy whenever possible. Child: 1 mth-12 yr: 7.5 mg/kg every 12 hr. Dose to be given via infusion into proximal vein.
Intravenous Susceptible infections Adult: 500 mg bid for 2-5 days. Dose to be infused over 60 minutes in a 0.2% solution; revert to oral therapy whenever possible. Child: 1 mth-12 yr: 7.5 mg/kg every 12 hr. Dose to be given via infusion into proximal vein.
|
||||||||||||||||||||||||||||||||||||
Contraindications |
Hypersensitivity. Patients receiving terfenadine, astemizole, pimozide, cisapride and ergot derivatives. Pregnancy; history of acute porphyria. | ||||||||||||||||||||||||||||||||||||
Warnings / Precautions |
Renal and hepatic impairment; macrolide cross-resistance; lactation, children. | ||||||||||||||||||||||||||||||||||||
Adverse Reactions |
GI upset, glossitis, stomatitis, altered taste; headache, dizziness, hallucinations, insomnia, other CNS effects; rash; hepatic dysfunction, Potentially Fatal: Pseudomembranous colitis, anaphylaxis, Stevens-Johnson syndrome. |
||||||||||||||||||||||||||||||||||||
Overdose Reactions |
GI symptoms e.g. abdominal pain, vomiting, nausea and diarrhoea. Prompt elimination of unabsorbed drug and supportive treatment should be instituted. Haemodialysis or peritoneal dialysis not expected to be helpful. | ||||||||||||||||||||||||||||||||||||
Drug Interactions |
May potentiate oral anticoagulant action. May elevate serum digoxin concentration. Potentially Fatal: Increases plasma concentrations of terfenadine or astemizole. Increases the risk of ventricular arrhythmias in patients with preexisting cardiac diseases. See Below for More clarithromycin Drug Interactions |
||||||||||||||||||||||||||||||||||||
Food Interactions |
Food may interfere with absorption though not clinically significant. | ||||||||||||||||||||||||||||||||||||
Mechanism of Actions |
Clarithromycin inhibits protein synthesis by binding to 50s ribosomal subunits of susceptible organisms. It has activity against susceptible streptococci and staphylococci as well as other species including B. catarrhalis, L. spp, C. trachomatis and U. urealyticum. Absorption: Rapidly absorbed from the GI tract (oral). Distribution: Widely distributed (concentrations exceed those in serum); enters the breast milk. Metabolism: Hepatic (extensive); converted to 14-hydroxyclarithromycin and other metabolites. Excretion: Via the bile into the faeces; via the urine (20-30% as unchanged, 10-15% as 14-hydroxyclarithromycin and other metabolites).3-4 hr and 5-7 hr (elimination half-life) |
||||||||||||||||||||||||||||||||||||
Administration |
Standard release tab & oral susp: May be taken with or without food. XL & MR tab: Should be taken with food. (Swallow whole, do not chew/crush.) |
||||||||||||||||||||||||||||||||||||
Storage Conditions |
Intravenous: Store at 15-25°C. | ||||||||||||||||||||||||||||||||||||
ATC Classification |
J01FA09 - clarithromycin ; Belongs to the class of macrolides. Used in the systemic treatment of infections. | ||||||||||||||||||||||||||||||||||||
Storage |
Intravenous: Store at 15-25°C. | ||||||||||||||||||||||||||||||||||||
Available As |
|
Clarithromycin
Post Review about Clarithromycin Click here to cancel reply.
Clarithromycin Containing Brands
Clarithromycin is used in following diseases
Drug - Drug Interactions of Clarithromycin
Latest News
- FDA approves Ruconest for treatment of hereditary angioedema
- FDA recommend against aspirin to prevent First Heart Attacks
- FDA approves Pomalyst (pomalidomide) for advanced multiple myeloma
- FDA approves three new drug treatments for type 2 diabetes
- Long-term consequences of vaginal delivery on the pelvic floor
No comments yet.