KLACID TABLET 250 mg

Aesica Queenborough Limited (UNITED KINGDOM)AbbVie S.r.l. (ITALY)🇸🇬 Health Sciences Authority

Approval Date: Jun 22, 1992
Approval ID: a4ea71f6dfcbd64c
Company: Aesica Queenborough Limited (UNITED KINGDOM)AbbVie S.r.l. (ITALY)
Type: Therapeutic

Approval Details

Approval Id: a4ea71f6dfcbd64c
Drug Name: KLACID TABLET 250 mg
Product Name: KLACID TABLET 250 mg
Approval Number: SIN07085P
Approval Date: 1992-06-22
Registrant: ABBOTT LABORATORIES (SINGAPORE ) PRIVATE LIMITED
Licence Holder: ABBOTT LABORATORIES (SINGAPORE) PRIVATE LIMITED
Drug Type: Therapeutic
Forensic Classification: Prescription Only
Dosage Form: TABLET, FILM COATED
Dosage: 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.
Route Of Administration: ORAL
Indication Info: 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: <ol> <li>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).</li> <li>Upper respiratory tract infections for example, sinusitis and pharyngitis.</li> <li>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.</li> <li>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).</li> <li>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.</li> </ol> Consideration should be given to national official guidance on the appropriate use of antibacterial agents.
Contraindications: 4.3. Contraindications <ul> <li>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).</li> <li>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).</li> <li>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).</li> <li>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)</li> <li>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).</li> <li>Clarithromycin should not be given to patients with electrolyte disturbances (hypokalemia or hypomagnesaemia, due to the risk of prolongation of the QT-interval).</li> <li>Clarithromycin should not be used in patients who suffer from severe hepatic failure in combination with renal impairment.</li> <li>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).</li> <li>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).</li> <li>Concomitant administration with ticagrelor, ivabradine or ranolazine is contraindicated.</li> <li>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).</li> </ul>
Atc Code: J01FA09
Atc Item Name: clarithromycin
Pharma Manufacturer Name: ABBOTT LABORATORIES (SINGAPORE ) PRIVATE LIMITED

Active Ingredients

Clarithromycin

250 mg

Clarithromycin

250 mg

Approved

Quick Info

Agency

HSA

Country

🇸🇬

Approval Date

Jun 22, 1992

Approval ID

a4ea71f6dfcbd64c

Type

Therapeutic

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