Rpharmy Memorial
Approved Hospital Formulary
Formulary Addition Requisition (Position 1)
Rpharmy Memorial Formweb Change Request (Position 2)
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Rpharmy Memorial
Approved Hospital Formulary
Formulary Addition Requisition (Position 1)
Rpharmy Memorial Formweb Change Request (Position 2)
Search by name
Additional search options
Search by class
Browse alphabetically
Select...
NUM
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
High Alert
Black Box Warning
LASA
Do Not Crush
Therapeutic Interchange
Non-Formulary
REMS
High Cost Drugs
Renal Dosing
Hazardous Drugs
Restricted
Questions & Suggestions (Position 3)
Webpage Links
Linezolid Zyvox Data Collection
LINEZOLID (ZYVOX) DATA COLLECTION SHEET
*Indicates Required Fields
*Patient Name
:
Admitting diagnosis :
Acct # :
Attending MD :
Age :
Prescribing MD :
Sex :
Service line :
Admit Date :
Discharge date :
Allergies :
Indication for Use (check all that apply)
Approved Indications
Clinically significant, documented vancomycin-resistant Enterococcus faecium infection
Clinically significant, documented methicillin-resistnat Staphylococci infections that are not treatable with any other agents
FDA-Approved Indications
Nosocomial pneumonia caused by:
MSSA
MRSA
Streptococcus pneumoniae (penicillin susceptible)
Community acquired pneumonia caused by:
Streptococcus pneumoniae (penicillin susceptible)
MSSA
Complicated skin and skin structure infections caused by:
MSSA
MRSA
Streptococcus pyogenes
Streptococcus agalactiae
Uncomplicated skin and skin structure infections caused by:
MSSA
Streptococcus pyogenes
Other Reasons for Use (please describe in detail)
Was organism confirmed by culture? Yes
No
Was culture obtained before drug initiated? Yes
No
Contraindications
Hypersensitivity to linozolid or any of its components
Dose and Administration
Date therapy initiated :
Date therapy ended :
IV Therapy
PO Therapy
Dose Given:
600 mg IV BID
400 mg IV BID (uncomplicated SSI only)
Dose Given:
600 mg PO BID
400 mg PO BID (uncomplicated SSI only)
Date patient eligible for PO therapy:
Date patient changed to PO therapy:
Did PHh recommend IV to PO conversion? Yes
No
Durg Interactions
(Does patient receive concomtantly)
Pseudoephedrine (increased BP)
Tramadol (increased seizure risk)
Monitoring
Date
WBC
S/B
Temp
H/H
Plt
Adverse Effects
(Check any/all that apply and describe reaction)
Hematologic (anemia, thrombocytopenia, leukopenia, pancytopenia, etc.):
Cardiovascular (HTN):
CNS (headache, neuropathy):
GI (n/v, diarrhea, abd pain):
Oral or vaginal yeast infection:
Dermatologic reactions:
Other:
Outcomes
Signs/symptoms of infection improved? Yes
No
Repeat cultures demonstrate organism eradication? Yes
No
Treatment discontinued due to (select all that apply):
Course of therapy complete/infection resolved
Inadequate response to therapy (specify which agent to which linezolid was changed)
Adverse effects/intolerant of drug
Discharged home
Expired
Other
Inadequate response comments:
Other comments:
Other Pertinent Patient Information