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Effective: 04/01/2020 C6499-A 12-2019 Page 1 of 2
Fax completed prior authorization request form to 800-854-7614 or submit Electronic Prior Authorization through
CoverMyMeds® or SureScripts.
All requested data must be provided. Incomplete forms or forms without the chart notes will be returned
Pharmacy Coverag
e Guideli
nes are available at www.mercycareaz.org/providers/completecare-forproviders/pharmacy
Janus Associated Kinase Inhibitors
Pharmacy Prior Authorization Request Form
Do not copy for future use. Forms are updated frequently.
REQUIRED: Office notes
, labs and medical testing relevant to request showing medical justification are required to support diagnosis
Member Information
Member Name (first & last): Date of Birth: Gender:
Male Female
Height:
Member ID: City: State: Weight:
Prescribing Provider Information
Provider Nam
e (first & last): Specialty: NPI#
DEA#
Office Address: City: State: Zip Code:
Office Contact: Office Phone Office Fax:
Dispensing Pharmacy Info
rmation
Pharmacy Name: Pharmacy Phone: Pharmacy Fax:
Requested Medication Information
Inrebic Jakaf
i Other, please specify:
Medication
request is NOT for an FDA- approved, or
compendia-supported diagnosis (circle one): Yes No
ICD-10 Code: Diagnosis:
What medication(s) have been tried and failed for diagnosis?
Are there any contraindications to formulary medications? Yes No
If yes, pleas
e specify:
Initial
Request
Continuation
of Therapy
Directions for Use: Strength: Dosage Form:
Quantity: Day Supply:
Duration
of Therapy/Use:
Turn-Around Time for Review
Standard – (2
4 hours) Urgent – If waiting 24 hours for a standard decision could seriously harm life, health,
or ability to regain maximum function, you can ask for an expedited decision.
Signature:
Clinical I
nformation
Has member been screened for
TB?
Yes No Was screeni
ng positive for latent TB? Yes No
Was treatment for latent TB receiv
ed
prior to initiating therapy?
Yes No N/A
Is there evidence showing that member ha
s a serious current ACTIVE infection? Yes No
Myelofibrosis
Is baseline PLT count at l
east 50 X 109/L? Yes No
Does member have TWO or more of the
following risk fac
tors?
Age >65 years Red Cell Tr
ansfusion
Constitutional symptoms (weight loss > 10% from bas
eline AND/OR unexplained fever
OR excessive sweats persisting > 1 month)
Hemoglobin <10g/dL WBC count ≥25
x 109/L
Peripheral Blood blasts >1% Platelet count <100 X 109/L
Unfavorable
karyotype [complex karyotype OR sole OR two abnorma
lities that include
trisomy 8, 7/7q-, i(17q), inv (3), 5/5q-, 12p- OR 11q23 rearrangement]
Additionally, for Inrebic
Is documentation showing signs of
severe hepatic
impairment (baseline
bilirubin >3-times ULN)?
Yes No Is documentation showing thiamine levels were
taken at baseline AND then periodically during
therapy to avoid Wernicke’s encephalopathy?
Yes No
Renewal Request ONLY
Was there spleen size re
duction ≥ 35%? Yes No Was there symptom improvement (≥50% reduction
in total symptom score from baseline)?
Yes No
Is there absence of disease progression? Yes No
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