Cubicin.com

For General Information About CUBICIN and Cubist Pharmaceuticals
Patient Assistance & Reimbursement
For questions about patient assistance and reimbursement, call 1-866-RXDAPTO (1-866-793-2786) and select option #2.

About CUBICIN Orders
For any questions regarding orders for CUBICIN, please call 1-888-8CUBIST (1-888-828-2478).

About CUBICIN Clinical Information
For more clinical information on CUBICIN, please contact our Medical Affairs Department at 1-866-793-2786.

About Clinical Trials
For more information on CUBICIN clinical trials, please contact our Medical Affairs Department at 1-866-793-2786.

The Daptomycin Reference Lab

Simply call the daptomycin reference lab (LSI) at 1-800-520-4890
An organism shipment kit will be shipped by next day service with a pre-paid completed air-bill for your convenience
Daptomycin MIC testing will be performed according to CLSI microbroth dilution methods and results will be sent by fax or email 2 days following receipt of the strain(s)
NOTE: Daptomycin MBC testing is also available upon request

The Daptomycin Reference Lab
Laboratory Specialists, Inc. (LSI)
1651 A Crossings Parkway
Westlake, OH 44145
Phone: 1-800-520-4890
Fax: 1-440-835-5786

Cubist Corporate Headquarters
Lexington Headquarters
65 Hayden Avenue
Lexington, MA 02421
781-860-8660 (Telephone)
781-861-0566 (Fax)

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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All rights reserved. CUBICIN is a registered trademark of Cubist Pharmaceuticals, Inc.
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