Advair / Dulera / Symbicort - Prior Authorization Request Form

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URGENT – 24 HOUR REQUEST
ADVAIR / DULERA / SYMBICORT
PRIOR AUTHORIZATION REQUEST FORM
Complete ENTIRE form and Fax to: 866-940-7328
SECTION A - PATIENT INFORMATION
Today‘s Date:
First Name:
Last Name:
Member ID #:
Address:
City:
State:
Zip:
Phone:
DOB:
Allergies:
Primary Insurance:
Policy #:
Group #:
NEW
CONTINUATION of THERAPY
Is the requested medication
or a
? If so, start date:_____________
Is this patient currently hospitalized?
Yes
No
SECTION B - PHYSICIAN INFORMATION
First Name:
Last Name:
M.D./D.O.
Address:
City:
State:
Zip:
Phone:
Fax:
NPI #:
Specialty:
Office Contact Name / Fax Attention to:
Medication:
Strength:
Directions for use:
ICD 10 Code:
Diagnosis (Please be specific & provide as much information as possible):
For Asthma:
Did the patient exhibit an inadequate response to treatment with at least a 30 day trial of an inhaled corticosteroid?
(e.g. Flovent, Asmanex, Pulmicort, Azmacort, or Qvar)
Yes____ No____ If yes, provide name of medication
and dates of therapy: _________________________________________________________________________
Did the patient experience an intolerance/adverse reaction to previous therapy or has a documented
contraindication to treatment with an inhaled corticosteroid? (e.g. Flovent, Asmanex, Pulmicort, Azmacort, or
Qvar) Yes____ No____ If yes, provide details:__________________________________________________________
Is this patient’s asthma diagnosis confirmed as severe persistent asthma? Yes____ No____ If yes, provide date
of diagnosis:________________________________________________________________________________
For COPD (Emphysema, Chronic Bronchitis):
Has the patient exhibited an inadequate response to treatment with at least a 60 day trial of EITHER a long-
acting beta2-agonist (e.g. Foradil, Serevent) OR an orally inhaled anticholinergic agent (e.g. Spiriva, Atrovent,
Combivent)?
Yes____ No____
If yes, provide name of medication and dates of therapy:
__________________________________________________________________________________________
Has the patient exhibited an intolerance/adverse reaction to previous therapy with at least a two-month trial of a
long-acting beta2-agonist (e.g. Foradil, Serevent) OR an orally inhaled anticholinergic agent (e.g. Spiriva,
Atrovent, Combivent)?
Yes____ No____
If yes, provide details:
__________________________________________________________________________________________
: ________________________
_______________
_______________
Physician Signature
Date:
Confidentiality Notice: This transmission contains confidential information belonging to the sender and UnitedHealthcare. This information is intended only for
the use of UnitedHealthcare. If you are not the intended recipient, you are hereby notified that any disclosure, copying, distribution or action involving the contents
of this document is prohibited. If you have received this telecopy in error, please notify the sender immediately.
Phone: 800-310-6826
Fax: 866-940-7328
Website:

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