Pharmacy Prior Authorization

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

Pharmacy Prior Authorization

3. Does the patient meet ALL of the following requirements? Y N

Pharmacy Prior Authorization

Please submit supporting medical documentation, notes and test results.

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

Thrombopoietin Receptor Agonists Prior Authorization with Quantity Limit Program Summary

Circle Yes or No Y N. (Note: requests without this information will not be accepted.) [If no, then no further questions.]

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

2. Is the patient responding to medication? Y N

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

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

Circle Yes or Y N. [Note: requests without this information will not be accepted.] [If no, then no further questions.

2. Is therapy prescribed by, or in consultation with, a hematologist and/or oncologist?

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

3. Has the member received the requested drug for less than 2 years? Y N

Prior Authorization. Drug Name (select from list of drugs shown) Viekira Pak (ombitasv-paritaprev-ritonav-dasabuv) Quantity Frequency Strength

Circle Yes or No Y N. [If yes, skip to question 30.] 2. Is this request for a child? Y N. [If no, skip to question 20.]

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

3. Has the member received the requested drug for less than 2 years? Y N

2. Does the member have a diagnosis of central precocious puberty? Y N

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

Pharmacy Prior Authorization

3. Have baseline A1c or fasting glucose, thyroid-stimulating hormone (TSH), and electrocardiography (EKG) been checked?

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

Pharmacy Prior Authorization

eltrombopag (Promacta )

Pharmacy Prior Authorization

2. Does the patient have a diagnosis of giant cell arteritis (GCA)? Y N

2. Is this request for a preferred medication? Y N

3. Is the prescribed dose within the Food and Drug Administration (FDA)- approved dosing for giant cell arteritis?

1. Has this plan authorized this medication in the past for this patient (i.e., previous authorization is on file under this plan)?

2. Does the patient have chronic urticaria? Y N

Circle Yes or No Y N. [If yes, skip to question 29.] 2. Is the request for Sandostatin LAR? Y N. [If no, skip to question 5.] Prior Authorization

Circle Yes or No Y N. [If no, then no further questions.]

2. Has this plan authorized this medication in the past for this member (i.e., previous authorization is on file under this plan)?

[If no, skip to question 10.] Y N. 2. Does the member have a diagnosis of Paget s disease of bone? Y N. [If no, skip to question 4.

3. Has bone specific alkaline phosphatase level increased OR does the member have symptoms related to active Paget s?

Pharmacy Prior Authorization

3. Has the patient had a sustained improvement in Pain or Function (e.g. PEG scale with a 30 percent response from baseline)?

Pharmacy Prior Authorization

Circle Yes or No Y N. [If no, skip to question 8.] 2. Has the patient been compliant with therapy as verified by the prescriber?

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.

PROMACTA (eltrombopag olamine) oral tablet and oral suspension

Pharmacy Prior Authorization

3. Does the patient continue to receive nutritional or psychological counseling? Y N

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

1. Has this plan authorized this medication in the past for this member (i.e., previous authorization is on file under this plan)?

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

2. Did the member receive this medication during a recent hospitalization? Y N

2. Did the patient receive this medication during a recent hospitalization? Y N

2. Has this plan authorized this medication in the past for this member (i.e., previous authorization is on file under this plan)?

2. Has this plan authorized this medication in the past for this member (i.e., previous authorization is on file under this plan)?

3. Does the member continue to receive nutritional or psychological counseling?

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

Promacta (eltrombopag)

2. Is the request for Alli, Xenical or Belviq? Y N. 3. Has the patient received 6 months or more of therapy? Y N

Ribavirin (Medicare Prior Authorization)

Promacta. Promacta (eltrombopag) Description

Prior Authorization. Drug Name (select from list of drugs shown) Gilenya (fingolomid) Quantity Frequency Strength. Physician Name:

2. Is the request for Humatrope? Y N [If no, skip to question 6.]

Drug Name (specify drug) Quantity Frequency Strength

Drug Name (specify drug) Quantity Frequency Strength

Promacta. Promacta (eltrombopag) Description

2. Has this plan authorized this medication in the past for this member (i.e., previous authorization is on file under this plan)?

2. Has this plan authorized this medication in the past for this member (i.e., previous authorization is on file under this plan)?

Drug Name (specify drug) Quantity Frequency Strength

Prior Authorization. Physician Name: Specialty: NPI Number: Physician Fax: Physician Phone: Physician Address: City, State, Zip:

[If yes, no further questions.]

Circle Yes or No Y N. [If yes, no further questions.]

2. Has this plan authorized this medication in the past for this member (i.e., previous authorization is on file under this plan)?

Cynthia Fata, MD, MSPH 6/23/15

9/9/2016. Drug Name (select from list of drugs shown) Bunavail Buccal Film (buprenorphinenaloxone) Suboxone Sublingual Film (buprenorphine-naloxone)

Form 2033 R3.0: Wiskott-Aldrich Syndrome Pre-HSCT Data

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

How I treat acquired aplastic anemia

What should I discuss with my health care provider before taking eltrombopag?

Atgam (lymphocyte immune globulin, anti-thymocyte globulin [equine])

Prior Authorization Criteria Form This form applies to Paramount Commercial Members Only. Non-Preferred Growth Hormone Products

QUICK REFERENCE Clinical Practice Guideline on the Evaluation and Management of Immune Thrombocytopenia (ITP)

TIBSOVO (ivosidenib) oral tablet

Committee Approval Date: May 9, 2014 Next Review Date: May 2015

Priority Health Medicare prior authorization form Fax completed form to: toll free, or

Address: City: State: ZIP code: Inferferon Product Requested (Include Strength):

Cigna Drug and Biologic Coverage Policy

Drug Class Prior Authorization Criteria Immune Globulins

Pharmacy Coverage Guidelines are subject to change as new information becomes available.

Attending Physician Statement- Aplastic Anaemia

Use of TPO mimetics for Indications Other Than ITP

Aplastic Anemia. is a bone marrow failure disease 9/19/2017. What you need to know about. The 4 major components of blood

Appendix to Notification Letter for rituximab and eltrombopag dated 20 February 2014

UKITP INITAL INFORMATION SHEET (2.4)

Hepatitis C Medications Hawaii PRIOR AUTHORIZATION REQUEST FORM

PRIOR AUTHORIZATION BYPASS Tanzeum (albiglutide) Bypass the Prior Authorization by Modifying the following Prescription Forms to the Patient's Needs

Texas Standard Prior Authorization Form Addendum

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

Transcription:

Pharmacy Prior Authorization MERC CARE (MEDICAID) Promacta (Medicaid) This fax machine is located in a secure location as required by HIPAA regulations. Complete/review information, sign and date. Fax signed forms to Mercy Care at 1-800-854-7614. When conditions are met, we will authorize the coverage of Promacta (Medicaid). Please note that all authorization requests will be reviewed as the AB rated generic (when available) unless states otherwise. Drug ame (circle drug) Promacta (eltrombopag) Other, specify drug Quantity Frequency Strength Route of administration Expected length of therapy Patient information Patient name: Patient ID: Patient Group o.: Patient DOB: Patient phone: Prescribing physician Physician name: Specialty: PI number: Physician fax: Physician phone: Physician address: City, state, zip: Diagnosis: ICD Code: Circle the appropriate answer for each question. Question Circle es or o Requests for Promacta will only be accepted by fax and with the appropriate medical records and lab results. Requests will not be taken over the phone. 1. Is this a request for a patient who is CURRETL taking Promacta? [If no, skip to question 16.] 2. Does the patient have a diagnosis of chronic idiopathic thrombocytopenic purpura (ITP)? Reference umber: C6582-A/ Effective Date: 09/01/2016 1

[If no, skip to question 6.] Circle es or o 3. Does the patient have a platelet count of at least 50,000/mm3? OTE: Lab results for platelets must be submitted with 4. Has the patient received 8 weeks of treatment with Promacta? 5. Is the dose of Promacta being increased? OTE: Dose should be increased by 25mg to a maximum of 75mg [o further questions.] 6. Does the patient have a diagnosis of aplastic anemia? [If no, skip to question 11.] 7. Does the patient have a platelet count of at least 50,000/mm3? OTE: Lab results for platelets must be submitted with 8. Has the patient received 16 weeks of treatment with Promacta? [If no, skip to question 10.] 9. Has the patient had a response to treatment indicated by at least OE of the following: A) Platelet count increase by at least 20,000/mm3 above baseline; B) Stable platelet count without requiring transfusions for at least 8 weeks; C) Hemoglobin increase by more than 1.5 g/dl above baseline; D) Reduction in RBC transfusions by at least 4 units for 8 consecutive weeks; E) Doubling of baseline AC or an increase in AC to above 500? OTE: Lab results to support a response to Promacta must be submitted with request. Requests without lab results will Reference umber: C6582-A/ Effective Date: 09/01/2016 2

not be accepted. Circle es or o [o further questions.] 10.Is the dose of Promacta being increased? OTE: The dose should be increased by 50mg every 2 weeks until platelets are at least 50,000/mm3 or to a maximum of 150mg. [o further questions.] 11.Does the patient have a diagnosis of Hepatitis C with thrombocytopenia? 12.Does the patient have a platelet count of at least 90,000/mm3? OTE: Lab results for platelets must be submitted with [If no, skip to question 14.] 13.Has a separate prior authorization been submitted to start antiviral treatment with pegylated interferon? [o further questions.] 14.Has the patient received 8 weeks of treatment with Promacta OR has the dose been increased to the maximum of 100mg? 15.Is the dose of Promacta being increased? OTE: The dose should be increased by 25mg every 2 weeks until platelets are at least 90,000 or to a maximum of 100mg. [o further questions.] 16.Does the patient have a diagnosis of idiopathic thrombocytopenic purpura (ITP)? [If no, skip to question 20.] 17.Has the patient had an insufficient response to corticosteroids, immunoglobulins, or splenectomy? Reference umber: C6582-A/ Effective Date: 09/01/2016 3

Circle es or o If yes, please document prior therapies or submit records: 18.Is Promacta being used to prevent major bleeding in a patient with a platelet count of less than 30,000/mm3? OTE: Promacta is not approved to achieve platelet counts in the normal range (i.e., 150,000-450,000/mm3) OTE: Lab results for platelets must be submitted with 19.Is the patient at least 1 year of age? [o further questions.] 20.Is Promacta requested to treat thrombocytopenia due to chronic hepatitis C infection in a patient with a platelet count of less than 90,000/mm3? OTE: Lab results for platelets must be submitted with [If no, skip to question 22.] 21.Does the patient require treatment for hepatitis C with a regimen that contains pegylated interferon? If yes, please document patient characteristics and rationale for requiring Peg-IF: [If yes, skip to question 25.] 22.Does the patient have a diagnosis of severe aplastic anemia confirmed by bone marrow biopsy showing less than 25% of normal cellularity? OTE: Medical records to support diagnosis must be submitted with request. Requests without records will not be accepted. [If yes, skip to question 24.] Reference umber: C6582-A/ Effective Date: 09/01/2016 4

Circle es or o 23.Does the patient have a diagnosis of severe aplastic anemia confirmed by bone marrow biopsy showing less than 50% of normal cellularity AD at least TWO of the following: A) Absolute neutrophil count (AC) less than 500/mm3; B) Platelet count less than 20,000/mm3; C) Absolute reticulocyte count less than 40,000/mm3? OTE: Medical records and lab results to support diagnosis must be submitted with request. Requests without records will not be accepted. 24.Is the anemia refractory to first line treatment with either hematopoietic cell transplantation OR immunosuppressive therapy with a combination of cyclosporine A and antithymocyte globulin (ATG)? OTE: Documentation of previous treatment must be included with request. 25.Is the patient at least 18 years old? Comments: I affirm that the information given on this form is true and accurate as of this date. Prescriber (Or Authorized) Signature Prescriber (Or Authorized) Signature Date Date Reference umber: C6582-A/ Effective Date: 09/01/2016 5