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CUBICIN (DAPTOMYCIN FOR INJECTION) 500MG [SIN13501P]
Active ingredients: CUBICIN (DAPTOMYCIN FOR INJECTION) 500MG
Product Info
CUBICIN (DAPTOMYCIN FOR INJECTION) 500MG
[SIN13501P]
Product information
Active Ingredient and Strength | DAPTOMYCIN - 500 MG/VIAL |
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Manufacturer and Country | OSO BIOPHARMACEUTICALS MANUFACTURING LLC (MANUFACTURE, PRIMARY PACKAGING) - UNITED STATES |
Registration Number | SIN13501P |
Licence Holder | MSD PHARMA (SINGAPORE) PTE. LTD. |
Forensic Classification | PRESCRIPTION ONLY MEDICINES |
Anatomical Therapeutic Chemical (ATC) code | NA |
1. INDICATIONS AND USAGE
CUBICIN is indicated for the treatment of the infections listed below.
1.1 Complicated Skin and Skin Structure Infections
Adult (≥18 years of age) and pediatric (1 to 17 years of age) patients with complicated skin and skin structure infections (cSSSI) caused by susceptible isolates of the following Gram-positive bacteria: Staphylococcus aureus (including methicillin-resistant isolates), Streptococcus pyogenes, Streptococcus agalactiae, Streptococcus dysgalactiae subsp. equisimilis, and Enterococcus faecalis (vancomycin-susceptible isolates only).
1.2 Staphylococcus aureus Bloodstream Infections (Bacteremia)
Adult patients (≥18 years of age) with Staphylococcus aureus bloodstream infections (bacteremia), including those with right-sided infective endocarditis (SAB/RIE), caused by methicillin-susceptible and methicillin-resistant isolates.
Pediatric patients (1 to 17 years of age) with S. aureus bloodstream infections (bacteremia) caused by methicillin-susceptible and methicillin-resistant isolates.
CUBICIN is not indicated for the treatment of left-sided infective endocarditis due to S. aureus. The efficacy of CUBICIN in patients with left-sided infective endocarditis due to S. aureus has not been demonstrated. The clinical trial of CUBICIN in patients with S. aureus bloodstream infections included limited data from patients with left-sided infective endocarditis; outcomes in these patients were poor. CUBICIN has not been studied in patients with prosthetic valve endocarditis.
CUBICIN is not indicated for the treatment of pneumonia [See 5 WARNINGS AND PRECAUTIONS, 5.2 Pneumonia – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information].
2. DOSAGE AND ADMINISTRATION
2.1 General
CUBICIN is given by intravenous (IV) administration.
CUBICIN is a sterile product contained in a single-dose vial.
2.2 Adults
Complicated Skin and Skin Structure Infections
CUBICIN 4 mg/kg is administered to adult patients intravenously in 0.9% sodium chloride for injection once every 24 hours for 7 to 14 days, either by injection over a 2-minute period or by infusion over a 30-minute period. Do not dose CUBICIN more frequently than once a day, and measure creatine phosphokinase (CPK) levels at baseline and at regular intervals (at least weekly). [See 3 INSTRUCTIONS FOR USE, 3.1 Preparation of CUBICIN for Administration – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information.]
Staphylococcus aureus Bloodstream Infections (Bacteremia)
CUBICIN 6 mg/kg is administered to adult patients intravenously in 0.9% sodium chloride for injection once every 24 hours for 2 to 6 weeks, either by injection over a 2-minute period or by infusion over a 30-minute period. Duration of treatment is based on the treating physician’s working diagnosis. Do not dose CUBICIN more frequently than once a day, and measure CPK levels at baseline and at regular intervals (at least weekly). [See 3 INSTRUCTIONS FOR USE, 3.1 Preparation of CUBICIN for Administration – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information.]
2.3 Pediatric Patients (1 to 17 Years of Age)
Complicated Skin and Skin Structure Infections
The recommended dosage regimens based on age for pediatric patients with cSSSI are shown in Table 1. CUBICIN should be administered intravenously in 0.9% sodium chloride for injection once every 24 hours for up to 14 days.
Unlike in adults, CUBICIN should not be administered by injection over a two (2) minute period in pediatric patients.

Staphylococcus aureus Bloodstream Infections (Bacteremia)
The recommended dosage regimens based on age for pediatric patients with S. aureus bloodstream infections (bacteremia) are shown in Table 2. CUBICIN should be administered intravenously in 0.9% sodium chloride for injection once every 24 hours for up to 42 days.

2.4 Renal Impairment
Daptomycin is eliminated primarily by the kidneys; therefore, an adjustment of CUBICIN dosage interval is recommended for adult patients with creatinine clearance (CLCR) <30 mL/min, including patients receiving hemodialysis or continuous ambulatory peritoneal dialysis (CAPD). The recommended dosing regimen for these adult patients is 4 mg/kg (cSSSI) or 6 mg/kg (S. aureus bloodstream infections) once every 48 hours. When possible, administer CUBICIN following the completion of hemodialysis on hemodialysis days. In adult patients with renal impairment, monitor both renal function and CPK more frequently than once weekly.
No dosage interval adjustment is required for adult patients with CLCR ≥30 mL/min.
Due to limited clinical experience, CUBICIN should only be used in adult patients with any degree of renal impairment (creatinine clearance <80 mL/min) when it is considered that the expected clinical benefit outweighs the potential risk. The response to treatment and renal function should be closely monitored in all adult patients with some degree of renal impairment.
Dose adjustments in adult patients with renal impairment by indication and creatinine clearance:

The dosage regimen for CUBICIN in pediatric patients with renal impairment has not been established.
4. CONTRAINDICATIONS
CUBICIN is contraindicated in patients with known hypersensitivity to daptomycin.
