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CORESM is a retrospective, multicenter registry which collects data and documents clinical outcomes in patients receiving CUBICIN. CORESM is not a controlled clinical trial and should not be used to predict success rates in clinical practice.

CORESM is important because it provides a real-world look at how CUBICIN is being used in a wide range of patient types within a clinical setting.

The documents below describe clinical outcomes with CUBICIN in patients with complicated skin infections, as well as bloodstream infections.

Use of CUBICIN in Patients with Surgical-Site Infections, as Reported in CORESM 2006*

CORESM is a retrospective, multicenter registry that collects data about patients who have received CUBICIN
Of 177 patients with surgical-site infections from 45 US institutions, 148 (84%) were evaluable with reported outcomes
Includes patients with surgical-site infections alone (n=134) or with concomitant bacteremia (n=13) or a complicated skin and skin structure infection (n=1)

Representative photographs; not from actual CORESM patients.

*Registry data may not reflect data obtained from randomized, prospective, double-blinded clinical trials.

CORESM 2006 Patients with Surgical-Site Infections: Risk Factors and Infection Types

*CLCR <30 mL/min.
CLCR=creatinine clearance.

CORESM 2006 Documented Pathogens, Treatment Setting, and Antibiotic Use in Patients with Surgical-Site Infections

Clinical Outcomes with CUBICIN in CORESM 2006 Registry Patients with Surgical-Site Infections

Overall clinical success = 96% (142 of 148)

*Clinical success is defined as clinical cure or clinical improvement.

*Clinical success is defined as clinical cure or clinical improvement.
†CL, <30 mL/min.

Clinical Outcomes with CUBICIN in CORESM 2006 Registry Patients with Surgical-Site Infections, cont'd

Download the 2006 Post-Marketing CORESM Registry for Surgical Site Infections
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Download the 2005 Post-Marketing CORESM Registry for S. aureus Bacteremia
Download the 2005 Post-Marketing CORESM Registry for Complicated Skin Infections
Download the 2004 Post-Marketing CORESM Registry for Complicated Skin Infections
Download CUBICIN Prescribing Information

Indications and Important Safety Information

CUBICIN® (daptomycin for injection) is indicated for the following infections:
- Complicated skin and skin structure infections caused by susceptible isolates of the following Gram-positive microorganisms: S. aureus (including methicillin-resistant isolates), Streptococcus pyogenes, Streptococcus agalactiae, Streptococcus dysgalactiae subspecies equisimilis, and Enterococcus faecalis (vancomycin-susceptible isolates only). Combination therapy may be clinically indicated if the documented or presumed pathogens include Gram-negative or anaerobic organisms
- S. aureus bloodstream infections (bacteremia), including those with right-sided infective endocarditis, caused by methicillin-susceptible and methicillin-resistant isolates. Combination therapy may be clinically indicated if the documented or presumed pathogens include Gram-negative or anaerobic organisms
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 or meningitis
Patients with persisting or relapsing S. aureus infection or poor clinical response should have repeat blood cultures. If a culture is positive for S. aureus, MIC susceptibility testing of the isolate should be performed using a standardized procedure, as well as diagnostic evaluation to rule out sequestered foci of infection. Appropriate surgical intervention (eg, debridement, removal of prosthetic devices, valve replacement surgery) and/or consideration of a change in antibiotic regimen may be required
CUBICIN is not indicated for the treatment of pneumonia
Clostridium difficile-associated diarrhea (CDAD) has been reported with the use of nearly antibacterial agents, including CUBICIN, and may range in severity from mild diarrhea to fatal colitis. CDAD has been reported to occur over 2 months post-antibiotic treatment. If CDAD is suspected, antibiotic treatment may need to be suspended
Patients receiving CUBICIN should be monitored for the development of muscle pain or weakness, particularly of the distal extremities. In patients who receive CUBICIN, creatine phosphokinase (CPK) levels should be monitored weekly, and more frequently in patients who received recent prior or concomitant therapy with an HMG-CoA reductase inhibitor. In patients with renal insufficiency, both renal function and CPK should be monitored more frequently. Patients who demonstrate unexplained elevations in CPK while receiving CUBICIN should be monitored more frequently
CUBICIN should be discontinued in patients with unexplained signs and symptoms of myopathy in conjunction with CPK elevation >1000 U/L (~5 x ULN), or in patients without reported symptoms who have marked elevations in CPK >2000 U/L (≥10 x ULN)
Most adverse events reported in CUBICIN clinical trials were mild to moderate in intensity. The most common CUBICIN adverse events were anemia, constipation, diarrhea, nausea, vomiting, injection-site reactions, and headache

Please refer to full Prescribing Information

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