Zyvox® Prior Authorization Worksheet
New York State MedicaidClinical Drug Review Program
Instructions
Program Information
Drugs included in the Clinical Drug Review Program (CDRP) require prior authorization.
A list of CDRP drugs is available at and at
Fax requests are NOT permitted for some CDRP drugs.
Prescriber Procedure
If your fax includes the standardized fax form, only the Member Name, ID, DOB, and Clinical Criterianeed to be completed and faxed as an attachment to process your request.
PA requests from 3rd party agencies to include faxes or any media are not allowed. Please have the prescribing physician or an agent employed by the prescribing practitionercontact our department for consideration of this request.
Additional documents required for approval include the following:
Documentation of culture and sensitivity results
Clinical notes, lab results, and documentation of the original diagnosis from an Infectious Disease Specialist must be included with this fax form.
Complete Blood Count (CBC) results
Following review of all of the required information, you will be contacted by the Clinical Support Center regarding prior authorization for Zyvox®.
If your fax includes the standardized fax form, only the Member Name, ID, DOB, and Clinical Criterianeed to be completed and faxed as an attachment to process your request.
Enrollee InformationEnrollee Name: / Date of Birth:
enrollee medicaid id number (2 letters, 5 numbers, 1 letter):
Prescriber Information
prescriber Name: / contact person:
prescriber 10-digit national provider identifier (NPI): / office Phone Number: / office Fax number:
Clinical Criteria
Name: / Zyvox®(linezolid)
strength:
directionS:
quantity[1]:
New prescription: / Yes No / If No, Date Therapy Initiated:
expected length of therapy[2]:
diagnosis2: / date of last evaluation for this diagnosis2:
What is the medication being prescribed for?
Were cultures and sensitivities performed confirming the diagnosis?
Yes No / (If YES, please include a copy of the culture and sensitivity results.)
If NO, what is the clinical rationale for prescribing Zyvox® without performing culture and sensitivities?
Are you, or have you consulted with, an Infectious Disease Specialist for this patient?[3]
Yes No
Was the patient recently hospitalized for the diagnosis you provided?
Yes No
If YES, was Zyvox® started in the hospital?
Yes No
Were there other antibiotics used to treat this diagnosis?
Yes No (If YES, provide all medications used and reason for discontinuation.)
Medication History
Please provide at least a three-month history of medication use.
Medication Trial/Previous Therapies / Date of Therapy / Strength / Frequency / Reason for Discontinuation
Start Date / End Date
Has the total duration of therapy with Zyvox®, including treatment in an inpatient setting, exceeded 14 days?
Yes No (If YES, please include a copy of the CBC taken after the patient initiated Zyvox® treatment.)
According to the Zyvox® prescribing information, myelosuppression (including anemia, leukopenia, pancytopenia, and thrombocytopenia) has been reported in patients receiving Zyvox®. Complete Blood Counts (CBCs) should be monitored weekly, particularly in patients receiving Zyvox® for longer than two weeks.
If YES, what is the rationale for exceeding 14 days of treatment?
Please be aware that The U.S. Food and Drug Administration (FDA) has received reports of serious central nervous system (CNS) reactions when Zyvox® is given to patients taking psychiatric medications that work through the serotonin system of the brain (serotonergic psychiatric medications). For more information and a list of the serotonergic psychiatric medications that can interact with Zyvox®, please visit
Attestation
I attest that Zyvox® is medically necessary for this patient and that all of the information on this form is accurate to the best of my knowledge.I attest that documentation of the above diagnosis and medical necessity is available for review if requested by New York Medicaid.
prescriber Signature / dateNote: Processing May Be Delayed if Information Submitted is Illegible or Incomplete.
Revision Date: September 24, 2018 / Prior Authorization Call Line 1-877-309-9493
For billing questions, call 1-800-343-9000.
For clinical concerns or Clinical Drug Program Review questions, visit and or
call 1-877-309-9493. / Page 1
[1] Prescriptions for Zyvox® are limited to a 14-day supply. Continuation beyond 14 days of therapy will require a new prescription and a new PA number.
[2] Diagnosis and length of therapy will be reviewed by a Clinical Pharmacist and/or Medical Director.
[3] Clinical notes, lab results, and documentation of the original diagnosis from an Infectious Disease Specialist must be included with the fax form.