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CRITERIA: UPDL Paramount Advantage (Medicaid) APPROVED: 03/01/2021 VERIFIED: 03/30/2021 REVIEWED: 03/30/2021 /CHRONIC IDIOPATHIC CONSTIPATION Prior Authorization Override Request PHARMACY FAX # 844-256-2025 • Pertinent office notes and past medical history must be submitted with the prior authorization request.

PATIENT INFORMATION Patient Name Date

Paramount ID DOB Gender: M/F

Medication Allergies

PROVIDER INFORMATION Prescriber Name NPI # DEA #

Prescriber Specialty Prescriber Address

Office Fax Phone Office Contact Name

MEDICATION REQUESTED Drug Name Strength Directions (Sig)

Duration of Therapy: Quantity Diagnosis Days: Months: Are you requesting brand (DAW): _ NO _ YES *PLEASE NOTE DAW REQUESTS REQUIRE RATIONALE- SEE BELOW

Is the Patient currently being treated with this medication?  Yes; Date started mm/dd/yy / /  No

(alosetron – generic of Lotronex) LINZESS (linaclotide) MOTEGRITY (prucalopride) MYTESI (crofelemer) TRULANCE (plecanatide) VIBERZI () XIFAXAN () ZELNORM (tegaserod) DULOLAX PERI-COLACE MIRALAX KONSYL SENOKOT BENTYL LOMOTIL LOTRONEX

MEDICAL JUSTIFICATION: Include Other Relevant Medications Tried and Results Please indicate previous treatment and outcomes below Previous Medication Strength Qty Directions (Sig) Dates (mmddyy to mmddyy) Reason for Discontinuation 1

2

3

4

CRITERIA: UPDL Paramount Advantage (Medicaid) APPROVED: 03/01/2021 VERIFIED: 03/30/2021 REVIEWED: 03/30/2021 CRITERIA FOR APPROVAL

1 Is this request for Linzess 145mcg OR 290mcg capsule? Yes No [If no, then skip to question 4.]

2 Is this request for continuation of therapy? Yes No [If no, then skip to question 7.]

3 Has the provider submitted clinical documentation and rationale supporting that Yes No the member’s disease state is currently controlled on the requested medication? [Note: Documentation is required for approval.]

[If no, then skip to question 7.]

4 Is this request for any of the following: A) Linzess 72mcg B) Motegrity, C) Yes No Trulance? [If yes, then skip to question 12.]

5 Is this request for Zelnorm? Yes No [If no, then skip to question 7.]

6 Is the requested drug being prescribed for a woman 64 years of age or younger? Yes No [If yes, then skip to question 12.]

7 Has the patient experienced an inadequate treatment response with no less than Yes No a 14 day trial of TWO preferred medications (which do not require prior approval)? [If yes, then skip to question 9.]

8 Is the patient unable to be changed to a preferred medication (which does not Yes No require prior approval) for any of the following acceptable reasons: A) Allergy, B) Contraindication or drug interaction, C) History of unacceptable or toxic side effects? [If no, then no further questions.]

9 Is the patient 18 years of age or older? Yes No [If no, then no further questions.] 10 Is this request for Mytesi? Yes No [If no, then no further questions.] 11 Does the patient have a diagnosis of non-infectious and evidence of Yes No concurrent HIV antiviral therapy? [No further questions]

12 Has the patient experienced an inadequate treatment response with no less than Yes No a 14 day trial of TWO step therapy products (i.e. Amitiza and Linzess 145mcg and 290mcg)? [Note: Step therapy product approval requires trial and failure or inability to use at least TWO preferred medications (not requiring prior approval).]

[If yes, then skip to question 14.]

CRITERIA: UPDL Paramount Advantage (Medicaid) APPROVED: 03/01/2021 VERIFIED: 03/30/2021 REVIEWED: 03/30/2021 13 Is the patient unable to be changed to a preferred medication for any of the Yes No following acceptable reasons: A) Allergy, B) Contraindication or drug interaction, C) History of unacceptable or toxic side effects? [If no, then no further questions.]

14 Is the patient 18 years of age or older? Yes No

RELEVANT MEDICAL RATIONALE FOR REQUEST/ADDITIONAL CLINICAL INFORMATION INCLUDING WHY PATIENT REQUIRES BRAND OVER GENERIC. (Attach Relevant Lab Results and Chart Notes)*

*In order to process this request, please complete all boxes completely.

This facsimile and any attached document are confidential and are intended for the use of individual or entity to which it is addressed. If you have received this in error, please notify us by telephone immediately 1-800-891-2520.