Regulatory Information
HSA regulatory responsibility and product classification details
Regulatory Responsibility
Product Classification
Formulation Information
TABLET, FILM COATED
**4.2 Posology and method of administration** **Dosage and Administration** **Respiratory tract/skin and soft tissue infections** **Adults:** The usual dose in adults and children 12 years of age or older, is 250 mg twice daily for 7 days although this may be increased to 500 mg twice daily for up to 14 days in severe infections. **Children older than 12 years:** As for adults. **Children younger than 12 years:** Use Klacid® Paediatric Suspension. The use of Klacid® IR has not been studied in children less than 12 years of age. **Eradication of _H. pylori_ (Adults)** Triple Therapy Regimen Clarithromycin 500 mg twice daily in conjunction with amoxicillin 1000 mg twice daily and a proton pump inhibitor in standard dose twice daily for seven days. Dual Therapy Regimen Clarithromycin 500 mg three times daily in conjunction with omeprazole 40 mg once daily for 14 days, followed by omeprazole 40 mg once daily for an additional 14 days. Supportive studies have been conducted with omeprazole 40 mg once daily for 14 days. **Elderly:** As for adults. **Renal Impairment:** In patients with renal impairment with creatinine clearance less than 30ml/min, the dosage of clarithromycin should be reduced by one-half, i.e., 250mg once daily or 250mg twice daily in more severe infections. Treatment should not be continued beyond 14 days in these patients. Klacid® may be given without regard to meals as food does not affect the extent of bioavailability.
ORAL
Medical Information
**4.1 Therapeutic Indications** Klacid® is indicated for treatment of infections caused by one or more susceptible organisms in adults and children 12 years and older. Indications include: 1. Lower respiratory tract infections for example, acute and chronic bronchitis, and pneumonia (see **section 4.4 and 5.1** regarding Sensitivity Testing – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_). 2. Upper respiratory tract infections for example, sinusitis and pharyngitis. 3. Klacid® is appropriate for initial therapy in community acquired respiratory infections and has been shown to be active _in vitro_ against common and atypical respiratory pathogens as listed in the microbiology section. 4. Klacid® is also indicated in skin and soft tissue infections of mild to moderate severity (see **section 4.4 and 5.1** regarding Sensitivity Testing – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_). 5. Klacid® in the presence of acid suppression effected by omeprazole is also indicated for the eradication of _H. pylori_ in patients with proven duodenal ulcers. See Dosage and Administration section. Consideration should be given to national official guidance on the appropriate use of antibacterial agents.
**4.3. Contraindications** - Hypersensitivity to macrolide antibiotic drugs or any of its excipients (see **section 6.1** – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_). - Concomitant administration of clarithromycin and any of the following drugs is contraindicated: astemizole, cisapride, pimozide, terfenadine as this may result in QT prolongation and cardiac arrhythmias including ventricular tachycardia, ventricular fibrillation, and _torsades de pointes_ (see **section 4.5** – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_). - Concomitant administration of clarithromycin and ergot alkaloids (e.g., ergotamine or dihydroergotamine) is contraindicated, as this may result in ergot toxicity (see **section 4.5** – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_). - Concomitant administration of clarithromycin and oral midazolam is contraindicated (see **section 4.5** – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_) - Clarithromycin should not be given to patients with history of QT prolongation (congenital or documented acquired QT prolongation) or ventricular cardiac arrhythmia, including _torsades de pointes_ (see **sections 4.4 and 4.5** – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_). - Clarithromycin should not be given to patients with electrolyte disturbances (hypokalemia or hypomagnesaemia, due to the risk of prolongation of the QT-interval). - Clarithromycin should not be used in patients who suffer from severe hepatic failure in combination with renal impairment. - Clarithromycin should not be used concomitantly with HMG-CoA reductase inhibitors (statins) that are extensively metabolized by CYP3A4 (lovastatin or simvastatin), due to the increased risk of myopathy, including rhabdomyolysis (see **section 4.4** – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_). - Clarithromycin (and other strong CYP3A4 inhibitors) should not be used concomitantly with colchicine (see **sections 4.4 and 4.5** – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_). - Concomitant administration with ticagrelor or ranolazine is contraindicated. - Concomitant administration of clarithromycin and lomitapide is contraindicated (see **section 4.5** – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_).
J01FA09
clarithromycin
Manufacturer Information
ABBOTT LABORATORIES (SINGAPORE ) PRIVATE LIMITED
Aesica Queenborough Limited
AbbVie S.r.l.
Active Ingredients
Documents
Package Inserts
1.4.3 Package Insert_Proposed Pristine_Klacid IR 250mg & Forte 500mg.docx
Approved: February 18, 2022