Advantage by Peach State Health Plan 2012 Prior Authorization Listing. Approved 10/23/2011 Effective October 2011

Similar documents
2014 Step Therapy Criteria (List of Step Therapy Criteria)

UnitedHealthcare Pharmacy Clinical Pharmacy Programs

IlliniCare Health MMAI (MMP) 2016 Step Therapy Criteria

2. Does the patient have a diagnosis of ulcerative colitis or Crohn s? Y N

See Important Reminder at the end of this policy for important regulatory and legal information.

2018 Pharmacy Directory

Atopic Dermatitis and Topical Antipsoriatics

2016 FORMULARY ADDENDUM NOTICE OF CHANGE

Xeljanz. Xeljanz, Xeljanz XR (tofacitinib) Description

Pharmacy Prior Authorization

CENTENE PHARMACY AND THERAPEUTICS NEW DRUG REVIEW 3Q17 July August

ACTEMRA (tocilizumab)

1 P a g e. Systemic Juvenile Idiopathic Arthritis (SJIA) (1.3) Patients 2 years of age and older with active systemic juvenile idiopathic arthritis.

3. Has the patient shown improvement in signs and symptoms of the disease? Y N

Cosentyx. Cosentyx (secukinumab) Description

2017 Medicare Part D Formulary Change

2. Is the patient responding to Remicade therapy? Y N

2018 Step Therapy (ST) Criteria

Helping You Stay Healthy

ORDER GUIDELINES. For delivery, please allow 7-10 business days from the time your order is placed.

Medication Policy Manual. Topic: Dupixent, dupilumab Date of Origin: March 10, Committee Approval: March 10, 2017 Next Review Date: May 2018

Dupixent (dupilumab)

See Important Reminder at the end of this policy for important regulatory and legal information.

MDwise Self-Administered Codes for Medical

2018 Step Therapy Criteria (List of Step Therapy Criteria)

Xeljanz (tofacitinib), Xeljanz XR (tofacitinib extended-release)

Stelara. Stelara (ustekinumab) Description

Otezla. Otezla (apremilast) Description

Eucrisa. Eucrisa (crisaborole) Description

ALBUTEROL - SCORE. Products Affected. Details. Step Therapy Criteria Golden State Medicare Health Plan, Golden (HMO) Last Updated: 09/01/2018

2018 Step Therapy Criteria (List of Step Therapy Criteria)

RAHF PFM ALPHANINE SD COAGULATION FACTOR IX J7193 COAGULATION FACTOR IX (RFIXFC)

CIMZIA (certolizumab pegol)

Regulatory Status FDA-approved indication: Orencia is a selective T cell co-stimulation modulator indicated for: (1)

Cimzia. Cimzia (certolizumab pegol) Description

Medication Policy Manual. Topic: Otezla, apremilast Date of Origin: May 9, 2014

Biologics for Autoimmune Diseases

Eucrisa. Eucrisa (crisaborole) Description

Circle Yes or No Y N. [If no, skip to question 7.] 2. Does the patient have a diagnosis of ulcerative colitis? Y N. [If no, skip to question 4.

Pharmacy Prior Authorization

2010 Drugs Requiring Prior Authorization

Drug Class Prior Authorization Criteria Therapeutic Agents in Rheumatic and Inflammatory Diseases

SAMPLE IgE: ESR: CRP: # Joints: %BSA: Height: Weight: BMI:

Regulatory Status FDA- approved indication: Simponi and Simponi ARIA are tumor necrosis factor (TNF) blockers indicated for the treatment of: (2-3)

2. Does the patient have a diagnosis of chronic idiopathic thrombocytopenic purpura (ITP)?

2. Does the patient have a diagnosis of Crohn s disease? Y N

Pharmacy Prior Authorization

HARVARD PILGRIM HEALTH CARE RECOMMENDED MEDICATION REQUEST GUIDELINES HUMIRA PEDIATRIC

Medication Policy Manual. Topic: Xeljanz, tofacitinib Date of Origin: January 21, 2013

3. Did the patient show evidence of remission by week 8 of Humira Y N therapy?

Health & Family. How Safe is Your Family? Molina Medicare Spring Contents. June is National Safety Month!

List 1 PRESCRIPTION DRUGS REQUIRING PRE-AUTHORIZATION LIBERTY HEALTH DRUG IDENTIFICATION NUMBER (DIN)

Pharmacy Prior Authorization

Pharmacy Management Drug Policy

Circle Yes or No Y N. [If yes, skip to question 13 REAUTHORIZATION REQUESTS]

2018 Medicare Part D Formulary Change

(tofacitinib) are met.

PROVIDER DIRECTORY This information is available for free in other languages.

The safety and effectiveness of Dupixent in pediatric patients have not been established (1).

IOWA MEDICAID DRUG UTILIZATION REVIEW COMMISSION 100 Army Post Road 5)

Drug Name Tier Drug Name Tier

First Name. Specialty: Fax. First Name DOB: Duration:

2014 Quantity Limits (QL) Criteria

Inflectra Frequently Asked Questions

Actemra. Actemra (tocilizumab) Description

Clinical Policy: Eltrombopag (Promacta) Reference Number: ERX.SPA.71 Effective Date:

CIMZIA (certolizumab pegol)

3. Has the patient shown improvement in signs and symptoms of the disease? Y N

2. Has the patient had a response to treatment? Y N. 3. Does the patient have a diagnosis of rheumatoid arthritis (RA)? Y N

ADALIMUMAB Generic Brand HICL GCN Exception/Other ADALIMUMAB HUMIRA GUIDELINES FOR USE INITIAL CRITERIA (NOTE: FOR RENEWAL CRITERIA SEE BELOW)

3. Does the patient have a diagnosis of rheumatoid arthritis (RA) with moderate to high disease activity?

Drug Class Prior Authorization Criteria Immune Globulins

Clinical Policy: Ustekinumab (Stelara) Reference Number: ERX.SPA.01 Effective Date:

Clinical Policy: Certolizumab (Cimzia) Reference Number: PA.CP.PHAR.247 Effective Date: 01/18 Last Review Date: 08/17 Line of Business: Medicaid

Prior Authorization Conditions for Approval of Enbrel (etanercept) Website Form Submit request via: Fax

Subject: Remicade (Page 1 of 5)

ARANESP ALBUMIN FREE ARANESP ALBUMIN FREE SURE ARICEPT ARICEPT ODT EXELON

eltrombopag (Promacta )

See Important Reminder at the end of this policy for important regulatory and legal information.

Clinical Policy: Dupilumab (Dupixent) Reference Number: ERX.SPA.49 Effective Date:

Clinical Policy: Abatacept (Orencia) Reference Number: ERX.SPA.123 Effective Date:

Divya Jain Arwindekar, DO Transplant Nephrologist Advocate Christ Medical Center & Associates in Nephrology

Clinical Policy: Baricitinib (Olumiant) Reference Number: CP.PHAR.135 Effective Date: Last Review Date: 11.18

Appendix 1: Frequently Asked Questions

Xeljanz. Xeljanz, Xeljanz XR (tofacitinib) Description

Pharmacy Management Drug Policy

Clinical Policy: Tofacitinib (Xeljanz, Xeljanz XR) Reference Number: ERX.SPA.110 Effective Date:

See Important Reminder at the end of this policy for important regulatory and legal information.

Drugs That Require Prior Authorization (PA) Before Being Approved for Coverage

Corporate Medical Policy

Clinical Policy: Sarilumab (Kevzara) Reference Number: CP.PHAR.346 Effective Date: Last Review Date: 11.18

Immunosuppression: evolution in practice and trends,

HARVARD PILGRIM HEALTH CARE RECOMMENDED MEDICATION REQUEST GUIDELINES

GROWTH HORMONE THERAPY

Post-operative pain following CABG surgery Allergic-type reaction to aspirin, NSAIDs, or sulfonamides

GROWTH HORMONE THERAPY

Xeljanz. Xeljanz, Xeljanz XR (tofacitinib) Description

Step Therapy Criteria

Transcription:

Advantage by Peach State Health Plan 2012 Approved 10/23/2011 Effective October 2011 Note to members: The prior authorization requirements are listed to provide you with information to discuss treatment options with your doctor. Medication Locator Instructions: 1. With the PDF open, on the Edit menu, click Find. 2. In the Find box type the name of the medication you want to find. 3. Click Find Next button until you find the medications you're looking for. H7173_MEM012_012 File and Use 10/23/2011

F or certain drugs Advantage by Peach State Health Plan (HMO SNP) requires you or your physician to get prior authorization for certain drugs. This means that you will need to get approval from Advantage by Peach State Health Plan before you fill your prescriptions. If you don t get approval, Advantage by Peach State Health Plan may not cover the drug. The prior authorization requirements are listed below to provide you with information to discuss treatment options with your physicians or health care prescribers. The is subject to change and may not be comprehensive. Some of the medications on the list may also be subject to additional plan coverage rules. ALBUTEROL NEBULIZER SOLN No Part B Ongoing if no Part B AMEVIVE Amevive is approved for the treatment of plaque psoriasis and all FDAapproved Trial and failure of one systemic therapy along with one topical treatment. Systemic therapy includes DMARDs or immunosuppressants including methotrexate or cyclosporine and topical treatment includes highpotency corticosteroids or calciprotriene. Approve at six month intervals. ARANESP Aranesp is approved for treatment of anemia in end stage renal disease and cancer to maintain hemoglobin levels between 10 and 12 grams per deciliter and for all other FDA-approved uses not Three months of hemoglobin monitoring and dosage titration to maintain hemoglobin levels within the range of 10 to 12. BOTOX Botox is approved for all FDA-approved uses not A prior authorization request for FDAapproved and labeled indications. CELLCEPT LIQUID AND INJECTABLE approved H7173 MEM012_012 File and Use 10/23/2011 Page 1 of 8

CROMOLYN NEBULIZER No Part B Ongoing if no Part B CYCLOSPORINE EGRIFTA Egrifta is approved for No Part B Diagnosis of severe lipodystrophy in HIV positive patients using antiretroviral drugs. Ongoing if no Part B Initial approval for 3 months. ELIDEL Elidel is approved for the treatment of all FDA approved One trial and failure and adherent use of medium to high potency topical corticosteroids, which may include (but not limited to) betamethasone, clobetasol, desonide, desoximetasone, fluocinolone, fluocinonide, fluticasone, halobetasol, or mometasone. FORTEO Forteo is approved for the treatment of osteoporosis and all FDA-approved otherwise excluded by Part D where patient has demonstrated a trial and failure or intolerance to oral alendronate. Evidence of adherent trial and failure of oral alendronate. GENGRAF approved INTAL NEBULIZER SOLN No Part B Ongoing if no Part B H7173 MEM012_012 File and Use 10/23/2011 Page 2 of 8

IPRATROPIUM/ ALBUTEROL NEBULIZER SOLN No Part B Ongoing if no Part B KINERET Kineret is approved for Trial and failure and adherent use of at least two oral diseasemodifying anti-rheumatic drugs or immunosuppressants, unless contraindicated. Systemic therapy may include methotrexate, leflunomide, hydroxychloroquine, cyclosporine, sulfasalazine, and azathioprine. LIDODERM PATCHES Lidoderm Patches are approved for all FDAapproved uses not LOTRONEX Lotronex is approved for Female patient with severe diarrheapredominant chronic irritable bowel syndrome of greater than 6 months duration METAPROTERENOL NEBULIZER SOLN. No Part B Ongoing if no Part B MYCOPHENOLATE MOFETIL approved NEORAL approved H7173 MEM012_012 File and Use 10/23/2011 Page 3 of 8

NORDITROPIN Growth hormone is approved for the treatment of growth hormone deficiency for all FDA-approved uses not Submission of information showing a growth hormone stimulation test reading of less than 10 µg/l in children and less than 5.1 µg/l in adults. NUTROPIN, NUTROPIN AQ Growth hormone is approved for the treatment of growth hormone deficiency for all FDA-approved uses not Submission of information showing a growth hormone stimulation test reading of less than 10 µg/l in children and less than 5.1 µg/l in adults. ORENCIA Orencia is approved for the treatment of all FDA approved Trial and failure and adherent use of at least two oral diseasemodifying anti-rheumatic drugs or immunosuppressants, unless contraindicated. Systemic therapy may include methotrexate, leflunomide, hydroxychloroquine, cyclosporine, sulfasalazine, and azathioprine. ORTHOCLONE OKT3 approved PEGASYS Pegasys is approved for the treatment of hepatitis C for treatment naïve patients with compensated liver disease and for patients diagnosed with hepatitis B. Treatment must be ordered by a gastroenterologist. Baseline viral load and submission of 12 week lab values showing a viral load decrease of at least a 2 log from baseline. 24 weeks for genotypes 2 and 3 or 48 weeks for genotypes 1 and 4. H7173 MEM012_012 File and Use 10/23/2011 Page 4 of 8

PEG-INTRON Peg-Intron is approved for the treatment of hepatitis C for treatment naïve patients with compensated liver disease and for patients diagnosed with hepatitis B. Treatment must be ordered by a gastroenterologist. Baseline viral load and submission of 12 week lab values showing a viral load decrease of at least a 2 log from baseline. 24 weeks for genotypes 2 and 3 or 48 weeks for genotypes 1 and 4. PROCRIT Procrit is approved for treatment of anemia in end stage renal disease and cancer to maintain hemoglobin levels between 10 and 12 grams per deciliter and for all other FDA-approved uses not Three months of hemoglobin monitoring and dosage titration to maintain hemoglobin levels within the range of 10 to 12. PROGRAF approved PROMACTA Promacta is approved for Platelet counts of less than 50,000 per microliter following standard treatment with corticosteroids, immunoglobulins, or after splenectomy. PROTOPIC Protopic is approved for One trial and failure and adherent use of medium to high potency topical corticosteroids, which may include (but not limited to) betamethasone, clobetasol, desonide, desoximetasone, fluocinolone, fluocinonide, fluticasone, halobetasol, or mometasone. H7173 MEM012_012 File and Use 10/23/2011 Page 5 of 8

PROVIGIL Provigil is approved for the treatment of narcolepsy, obstructive sleep apnea/hypopnea syndrome, shift work sleep disorder. and all FDA-approved otherwise excluded by Evidence supporting diagnosis of an FDA approved indication. RANEXA Ranexa is approved for Trial and failure of longacting nitrate therapy. RAPAMUNE approved REGRANEX Regranex is approved for A diagnosis of diabetic neuropathic ulcers that extend into the subcutaneous tissue or beyond and have an adequate blood supply. Approve for three months initially, followed by one three month approval if ulcer has shown a decrease in size. RESTASIS Restasis is approved for Diagnosis of decrease tear production due to ocular inflammation associated with keratoconjunctivitis sicca. SAIZEN Treatment for growth hormone deficiency evidenced by growth hormone stimulation test results, bone age measurement and growth velocity as appropriate to age. Submission of information showing a growth hormone stimulation test reading of less than 10 µg/l in children and less than 5.1 µg/l in adults. SANDIMMUNE approved H7173 MEM012_012 File and Use 10/23/2011 Page 6 of 8

SEROSTIM Serostim is approved for uses not Diagnosis appropriate to FDA labeled indications. SIMULECT approved SOMAVERT Somavert is approved for uses not Confirmed diagnosis of acromegaly inadequate response to surgery and/or radiation therapy and bromocriptine. SYMLIN TACROLIMUS Treatment for growth hormone deficiency evidenced by growth hormone stimulation test results, bone age measurement and growth velocity as appropriate to age. Diabetes type 1 patients: A1c reading greater than 7 and adherent use of short acting and basal insulins. Diabetes type 2 patients: A1c reading greater that 7 and evidence of prior adherent use of standard first-line therapy with either metformin plus a sulfonylurea or metformin plus a thiazolidinedione. approved TEV-TROPIN Growth hormone is approved for the treatment of growth hormone deficiency for all FDA-approved uses not Submission of information showing a growth hormone stimulation test reading of less than 10 µg/l in children and less than 5.1 µg/l in adults. THYMOGLOBULIN approved H7173 MEM012_012 File and Use 10/23/2011 Page 7 of 8

XENAZINE Xenazine is approved for Diagnosis of chorea associated with Huntington disease. XOLAIR Xolair is approved for the treatment of all FDAapproved Prescription history evidence of adherence to inhaled corticosteroids along with long-acting beta agonists for at least 3 months prior to request. Submission of IgE serum levels between 30 and 700 IU per milliliter. XOPENEX NEBULIZER SOLN No Part B Ongoing if no Part B ZORTRESS approved transplant You can find out if your drug has any additional requirements or limits by looking in the Advantage by Peach State Health Plan Comprehensive Formulary. For a complete listing of drugs covered by Advantage by Peach State Health Plan, please visit our web site at www.pshp.com or call 1-877-725-7748, Monday through Sunday 8:00 am to 8:00 pm. TTY/TDD users should call 1-800-659-7487. This information is available for free in other languages. Please contact Member Services at 1-877-725-7748 for additional information. Advantage by Peach State Health Plan is Coordinated Care plan with a Medicare Advantage contract and a contract with the Georgia Medicaid program. This information is available for free in other languages. Please contact our Member Services number at 1-877-725-7748 for additional information. (TTY users should call 1-800-659-7487). Hours are Monday through Sunday 8:00AM to 8:00PM. Esta información está disponible gratuitamente en otros idiomas. Comuníquese con nuestro número de servicios para los miembros llamando al 1-877-725-7748 para obtener información adicional. (Los usuarios de TTY deben llamar al 1-800-659-7487). El horario es de lunes a domingo de 8:00 a. m. a 8:00 p.m. H7173 MEM012_012 File and Use 10/23/2011 Page 8 of 8