<<

CRITERIA: UPDL Paramount Advantage (Medicaid) APPROVED: 01/01/2021 VERIFIED: 02/26/2021 REVIEWED: 02/01/2021 SKELETAL MUSCLE RELAXANTS, NON- 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

( – generic of Soma) (carisoprodol compound – generic of Soma (carisoprodol compound with – generic of compound) Soma compound with codeine) ( 375 mg and 750 mg) ( ER – generic of Amrix) (cyclobenzaprine 7.5mg - generic of Fexmid) LORZONE (chlorzoxazone) ( – generic of Skelaxin) ( - generic of Norflex) (orphenadrine compound - generic of Norgesic) (orphenadrine compound forte - generic of Norgesic ( capsules – generic of Zanaflex) Forte) LIORESAL () PARAFON FORTE (chlorzoxazone) DANTRIUM () ROBAXIN () ZANAFLEX (tizanidine capsules) SOMA (carisoprodol) SOMA COMPOUND (carisoprodol compound) SOMA COMPOUND W/CODEINE (carisoprodol FEXMID (cyclobenzaprine) compound with codeine) AMRIX (cyclobenzaprine ER) SKELAXIN (metaxalone) NORFLEX (orphenadrine) JORGESIC NORGESIC FORTE (orphenadrine compound forte)

MEDICAL JUSTIFICATION: Include Other Relevant 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: 01/01/2021 VERIFIED: 02/26/2021 REVIEWED: 02/01/2021

CRITERIA FOR APPROVAL

1 Has the patient experienced an inadequate treatment response to at least a 30 Yes No day trial with a preferred medication (which does not require prior approval)? [If yes, then go to question 3.]

2 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.]

3 Is the request for a carisoprodol (Soma) product or a combination product that Yes No contains carisoprodol? [If no, then no further questions.]

4 Would any other or agent used to treat fibromyalgia or any Yes No musculoskeletal condition serve the clinical needs of the patient?

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.