Important Safety Information
Prescribing Information
Medication Guide
Clinical References
References Request
Why Vibativ
Potency
Dual MOA
Dosing
Safety Info
HABP/VABP
Treating HABP/VABP
Subgroups
Lung Penetration
Concurrent Bacteremia
cSSSI
TREATING cSSSI
Subgroups
Tissue Penetration
Concurrent Bacteremia
Real World Results
Outcomes
Setting Of Care
Pathogens
Order of Therapy
Adverse Effects
Access
Order
Storage and Handling
Billing
MIC Test Strips
Patient Identifier
Why Vibativ
Potency
Dual MOA
Dosing
Safety Info
HABP/VABP
Treating HABP/VABP
Subgroups
Lung Penetration
Concurrent Bacteremia
cSSSI
TREATING cSSSI
Subgroups
Tissue Penetration
Concurrent Bacteremia
Real World Results
Outcomes
Setting Of Care
Pathogens
Order of Therapy
Adverse Effects
Access
Order
Storage and Handling
Billing
MIC Test Strips
Patient Identifier
ONCE-DAILY DOSING WITH NO THERAPEUTIC DRUG-LEVEL MONITORING REQUIRED
1
No loading dose required
Administered over a 60-minute period
Dosed 10 mg/kg every 24 hours
For 7 to 14 days in cSSSI
For 7 to 21 days in HABP/VABP
Duration of therapy should be guided by the severity and site of the infection, and by the patient’s clinical progress
Monitoring of serum creatinine is recommended in all patients
Monitoring Renal Function
Monitor renal function in all patients as new onset or worsening renal impairment has occurred
Prior to initiation of treatment
During treatment (at 48- to 72-hour intervals or more frequently, if clinically indicated)
At end of treatment
Other Considerations
No drug interactions were observed
VIBATIV shares the same potential as vancomycin for infusion reactions if not infused over at least 60 minutes
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