Injectable drugs requiring prior authorization all plans Updated January 2012 |
Click the drug name to get the PA form |
Code |
Benefit |
Use |
Criteria for coverage |
| Actemra (tocolizumab) |
J3262 |
Medical |
Rheumatoid arthritis |
- Moderate to severe rheumatoid arthritis in adults
- Trial of at least one self-injectable anti-TNF
- Negative TB test (must be done yearly)
- Pretreatment labs completed and within normal limits (CBC with diff, LFTs, Lipid panel)
- Patient must not be receiving Actemra in combination with and other biologic drug
|
| Acthar (corticotrophin) |
J0800 |
Pharmacy |
Up to 40 units; treatment for infantile spasms Length of initial authorization: 2 weeks Length of continuation authorization: 4 weeks |
Diagnosis of infantile spasms |
| Adcetris (brentuximab) |
J9999 C9287 |
Medical |
Treatment of Hodgkins lymphoma and anaplastic large cell lymphoma |
One of the following diagnoses: - Adult patients with Hodgkin lymphoma after failure of autologous stem cell transplant (ASCT) or after failure of at least two prior multi-agent chemotherapy regimens
- Adult patients with Systemic anaplastic large cell lymphoma (ALCL) after failure of at least one prior multi-agent chemotherapy regimen
|
| Aloxi (palonosetron) |
J2469 |
Medical |
Per 10 mg; antiemetic; PA required ONLY for home infusion providers |
|
| Amevive (alefacept)2 |
J0215 |
Medical |
Per 10mg; biologic treatment for moderate to severe chronic plaque psoriasis Length of initial authorization: 3 months Length of continuation authorization: 1 year Two courses of therapy must be separated by at least 3 months |
- Diagnosis of chronic moderate-to-severe plaque psoriasis affecting >10% of BSA (unless hands, feet, head and neck, or genitalia)
- Documented trial of one topical agent, one systemic treatment, AND phototherapy
|
| Anzemet (dolasetron) |
J1260 |
Medical |
Per 10 mg; antiemetic; PA required ONLY for home infusion providers |
See PA form for Medicare |
| Aralast (alpha 1 proteinase inhibitor - human) |
J0256 |
Medical |
Alpha-antitrypsin deficiency |
- Diagnosis of congenital alpha 1-antitrypsin deficiency
- Clinically evident emphysema
- FEV1 30-65% predicted
- Serum AAT level < 11mM/L (< 60 mg/dL)
|
| Arzerra (ofatumumab) |
J9032 |
Medical |
Treatment of refractory CLL |
- Diagnosis of CLL
- Trial and failure of fludarabine (Fludara) and alemtuzumab (Campath)
|
| Benlysta (belimumab) |
J0490 |
Medical |
Treatment of SLE |
- Active, auto-antibody positive SLE
- Baseline SELENA-SLEDAI score of 6 or more
- Free of severe nephritis, CNS manifestations, and chronic infections
- Currently receiving standard therapy for at least 3 months
- Not receiving any biologic therapy or intravenous cyclophosphamide
|
Click the drug name to get the PA form |
Code |
Benefit |
Use |
Criteria for coverage |
Boniva (ibandronate sodium)7
|
J1740 |
Medical |
Injection 1 mg for treatment of osteoporosis Length of authorization: 2 years (given one injection every 3 months)
|
- Diagnosis of postmenopausal osteoporosis (T-score < -2.5)
- Clinical trial of Fosamax, Actonel, and Reclast
See PA form for Medicare |
| Botox (Botulinum toxin type A)1 |
J0585 |
Medical |
Per unit, for various neuro-muscular uses: see PA form for covered conditions Length of authorization: 1 year (given one injection every 3 months) Injections must be separated by at least 90 days |
- See PA form for a list of covered indications
- Treatment for anal fissures and headache diagnoses require a clinical trial of conventional therapies
See PA form for Medicare |
| Cimzia (certolizumab) |
J0718 |
Medical or Pharmacy |
Per 1mg; treatment of moderate to severe Crohn's disease and rheumatoid arthritis Medical coverage if administered by health professional Pharmacy coverage if self-injected |
- Documented therapeutic trial and clinical failure with either Enbrel or Humira
- Diagnosis of Rheumatoid arthritis with documented therapeutic trial of at least one DMARD AND documented therapeutic trial and clinical failure with either Enbrel or Humira
- Diagnosis of Crohn's Disease with documented therapeutic trial of at least two of the following formulary alternatives: corticosteroids, sulfasalazine, osalazine, and mesalamine AND documented therapeutic trial and clinical failure with Humira
- Negative TB test (must be done yearly)
See Medical necessity form for complete details. |
| Dysport (abobotulinumtoxin A)1 |
J0586 |
Medical |
Per 5 units, for various neuro-muscular uses: see PA form for covered conditions Length of authorization: 1 injection Injections must be separated by at least 90 days |
- See PA form for a list of covered indications
- Treatment for anal fissures and headache diagnoses require a clinical trial of conventional therapies
See PA form for Medicare |
| Enbrel (etanercept)3 |
J1438 |
Pharmacy |
Treatment of rheumatoid arthritis, juvenile RA, ankylosing spondylosis, plaque psoriasis, psoriatic arthritis, and ankylosing spondylitis Length of initial authorization: 3 months Length of continuation authorization: 1 year (3 months for plaque psoriasis)
|
- Diagnosis of rheumatoid arthritis, juvenile RA, ankylosing spondylosis, plaque psoriasis, psoriatic arthritis, or ankylosing spondylitis
- Negative TB test (provided on an annual basis)
- Treatment failure with one or more DMARD (except ankylosing spondylitis and plaque psoriasis)
- Ankylosing spondylitis requires failure of at least 2 NSAIDs, intra-articular steroids, and sulfasalazine in patients with peripheral arthritis
- Plaque psoriasis affecting > 10% of BSA (unless hands, feet, head and neck, or genitalia) and a documented trial of one topical agent, one systemic treatment, and phototherapy
|
| Erbitux (cetuximab) |
J9055 |
Medical |
Treatment of advanced metastatic colorectal cancer and head and neck cancer Length of authorization: 4 injections
|
- Patient is 18 years of age
- Diagnosis of metastatic colorectal cancer or sqamous cell carcinoma of the head and neck
- Documented KRAS negative mutation status for colorectal cancer
- Used in combination with other therapy or as a single agent in members that have failed or been intolerant to other therapy
|
| Extavia (interferon beta 1b) |
J1830 |
Pharmacy |
Treatment of multiple sclerosis |
Requires a trial and failure with both Rebif and Copaxone |
Fabrazyme (agalsidase beta) |
J0180 |
Medical |
Treatment of Fabry disease Length of authorization: 1 year |
Diagnosis of Fabry disease |
| Firmagon (degrelix) |
J9155 |
Medical |
Treatment of prostate cancer |
- Diagnosis of prostate cancer
- Trial and failure with leuprolide (Lupron Depot), goserelin (Zoladex) or triptorelin (Trelstar Depot) with or without anti-androgen therapy for the first 30 days
|
Click the drug name to get the PA form |
Code |
Benefit |
Use |
Criteria for coverage |
| Forteo (teriparatide)2,3 |
J3110 |
Pharmacy |
Treatment of osteoporosis Length of authorization: 2 years
|
- Diagnosis of postmenopausal osteoporosis in women or primary or hypogonadal osteoporosis in men
- Clinical trial and failure with Fosamax (alendronate) and Actonel
|
| Glassia (alpha 1 proteinase inhibitor - human) |
J0257 |
Medical |
Alpha-antitrypsin deficiency |
- Diagnosis of congenital alpha 1-antitrypsin deficiency
- Clinically evident emphysema
- FEV1 30-65% predicted
- Serum AAT level < 11mM/L (< 60 mg/dL)
|
Human growth hormone3: Preferred: Norditropin
Other: Nutropin Nutropin AQ Humatrope Saizen Genotropin Serostim Zorptive (somatropin)3 Protropin |
J2941 J2940 (Protropin) |
Pharmacy |
Per 1 mg; human growth hormone (HGH) Length of initial authorization: 1 year Authorization of a non-preferred agent requires a clinical failure of a preferred agent
|
- Pediatrics: Diagnosis of idiopathic growth hormone deficiency (requires submission of appropriate lab tests) or Turner's syndrome
- Adults: Documented growth hormone deficiency and hypothalamic pituitary disease, history of cranial radiation, pituitary surgery, or continued treatment of childhood growth hormone deficiency
|
| Humira (adalimumab)2,3 |
J0135 |
Pharmacy |
Treatment of rheumatoid arthritis, juvenile idiopathic arthritis, ankylosing spondylitis, Crohn's disease, and plaque psoriasis Length of initial authorization: 3 months Length of continuation authorization: 1 year (3 months for plaque psoriasis) |
- Diagnosis of rheumatoid arthritis, juvenile RA, ankylosing spondylosis, Crohn's disease, plaque psoriasis, psoriatic arthritis, or ankylosing spondylitis
- Negative TB test (provided on an annual basis)
- Treatment failure with one or more DMARD (except Crohn's disease, ankylosing spondylitis and plaque psoriasis)
- Crohn's disease requires treatment failure with two or more conventional therapies
- Ankylosing spondylitis requires failure of at least 2 NSAIDs, intra-articular steroids, and sulfasalazine in patients with peripheral arthritis
- Plaque psoriasis affecting > 10% of BSA (unless hands, feet, head and neck, or genitalia) and a documented trial of one topical agent, one systemic treatment, AND phototherapy
|
Hyaluronic acid derivatives4 Preferred: Euflexxa (no PA required for Euflexxa) PA does not apply to Priority Health Medicare plans |
J7323 |
Medical |
Euflexxa: Treatment of osteoarthritis of the knee(s) |
- Diagnosis of osteoarthritis of the knee(s)
- Clinical trial and failure of at least two other pharmacologic therapies (NSAIDs, COX-2 selective NSAIDs, acetaminophen, IA corticosteroids, tramadol)
- Euflexxa is the preferred product. All other hyaluronic acid derivative products require a therapeutic trial and clinical failure with Euflexxa.
- Prior authorization is not required for Euflexxa
|
J7321 |
Medical |
Hyalgan or Supartz: Treatment of osteoarthritis of the knee(s) Length of authorization: 3-5 injections |
J7322 |
Medical |
Synvisc or Synvisc One: Treatment of osteoarthritis of the knee(s) Length of authorization: 1-5 injections |
J7324 |
Medical |
Orthovisc: Treatment of osteoarthritis of the knee(s) Length of authorization: 3-5 injections |
J7326 |
Medical |
Gel-One: Treatment of osteoarthritis of the knee(s) |
Ilaris (canakinumab)
|
J0638 |
Medical
|
Medical treatment of Familial Cold Autoinflammatory Syndrome (FCAS) and Muckle-Wells Syndrome (MWS) C-code billable by facility only
|
One of the following diagnoses: Cryopyrin-Associated Periodic Syndromes (CAPS): including Familial Cold Autoinflammatory Syndrome (FCAS) and Muckle-Wells Syndrome (MWS) in patients ≥ 4 years old. |
Click the drug name to get the PA form |
Code |
Benefit |
Use |
Criteria for coverage |
Increlex
|
J2170
|
Medical
|
Treatment of insulin-like growth factor-1 deficiency Length of authorization: 1 year
|
- Diagnosis of severe primary insulin-like growth factor-1 deficiency or growth hormone gene deletion who have developed neutralizing antibodies to GH
- Must be evaluated by a pediatric endocrinologist
|
| IVIG (immune globulin) - various brand names7 |
J1561 |
Medical |
Gamunex |
See PA form for covered indications |
J1566 |
Immune globulin, lyophilized (e.g., powder), 500 mg IV |
J1568 |
Injection, immune globulin (Octagam), intravenous, non-lyphilized (e.g. liquid), 500 mg |
J1569 |
Gammagard liquid |
J1572 |
Flebogamma |
90283 |
Immune globulin, 100 mg subcutaneous |
J1459 |
Privigen |
J1562/90284 |
Vivaglobin (SC1g), 100 mg, subcutaneous |
J1559 |
Hizentra |
J1557 |
Gammaplex |
| Jevtana (carbazitaxel) |
J9043 |
Medical |
Treatment of hormone-refractor metastatic prostate cancer |
- Diagnosis of hormone-refractory metastatic prostate cancer
- Prior use of a docetaxel-containing treatment regimen
- Serum prostate-specific antigen (PSA) ≥ 5 ng/mL
- Two sequential rising PSA levels obtained 2–3 weeks apart or other evidence of disease progression
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
- Serum testosterone < 50 ng/dL
- Jevtana will not be authorized for patients with any of the following:
- Congestive heart failure
- Myocardial infarction within the last 6 months
- Uncontrolled cardiac arrhythmias, angina pectoris, and/or hypertension
- ECOG performance status ≥ 3
|
| Kineret (anakinra)3 |
J3490 |
Pharmacy |
For treatment of moderate to severe symptoms of rheumatoid arthritis Length of initial authorization: 3 months Length of continuation authorization: 1 year |
- Diagnosis of moderate to severe rheumatoid arthritis
- Negative TB test (provided on an annual basis)
- Treatment failure with one or more DMARD
- Treatment failure with Enbrel
|
| Krystexxa (pegloticase) |
J2507 |
Medical |
For treatment of chronic gout refractory to conventional therapy Length of initial authorization: 3 months Length of continuation authorization: 1 year |
- Symptomatic gout and has experienced three or more flares within the past 18 months
- Patient has at least one gout tophus or has gouty arthritis
- Therapeutic trial (at least 6 months) and clinical failure of conventional therapy
- Continuation requires SUA level ≤ 6 mg/dL
|
| Lucentis (ranibizumab)6 |
J2778 |
Medical |
Treatment of AMD and RVO |
Documented therapeutic trial and clinical failure with Avastin (bevacizumab) |
| Macugen (pegaptinib)6 |
J2503 |
Medical |
Treatment of AMD |
Documented therapeutic trial and clinical failure with Avastin (bevacizumab) |
| Makena (hydroxyprogesterone caproate)7 |
J1725 |
Medical |
Prevention of preterm birth |
- Not covered
- Compounded 17P (17 alpha-hydroxyprogesterone caproate) is covered, no PA required
|
| Myobloc (Botulinum toxin type B)1 |
J0587 |
Medical |
Per 100 units; for treatment of cervical dystonia Length of authorization: 1 year, given as 1 injection every 3 months Injections must be separated by at least 90 days |
- See PA form for a list of covered indications
- Treatment for anal fissures and headache diagnoses require a clinical trial of conventional therapies
See PA form for Medicare |
| Nplate (romiplostim) |
J2796 |
Medical |
For treatment of chronic immune (idiopathic) thrombocyctopenia (ITP) Starting Dose 1 mck/kg SC weekly. Median dose to achieve response: 2-3 mcg/kg weekly. (Max dose 10 mcg/kg weekly). Dose to achieve platelet count above 50 x 109/L (not to normal platelet levels). Length of initial authorization: 4 injections Length of continuation authorization: If platelet count increases to a level sufficient to avoid clinically important bleeding, approved for an additional 4 injections |
- Diagnosis of chronic immune (idiopathic) thrombocytopenic purpura (ITP)
- Patient has had an insufficient response to corticosteroids, immunoglobulins or splenectomy
- Current platelet count < 50 x 109/L with clinical risk of bleeding
|
| Nulojix (belatacept) |
C9286 J3590 |
Medical |
For treatment of Hodgkins lymphoma and anaplastic large cell lymphoma |
- New kidney transplant (started Day 1 after transplant), given in combination with basiliximab induction, mycophenolate mofetil, and corticosteroids
- Seropositive for Epstein-Barr virus (EBV)
- Allergy or intolerance to tacrolimus and/or cyclosporine
|
Click the drug name to get the PA form |
Code |
Benefit |
Use |
Criteria for coverage |
| Orencia (abatacept)6 |
J0129 |
Medical |
For treatment of moderate to severe symptoms of rheumatoid arthritis Length of initial authorization: 3 months Length of continuation authorization: 1 year
|
- Diagnosis of moderate to severe rheumatoid arthritis
- Negative TB test (provided on an annual basis)
- Treatment failure with one or more self-injectable TNF antagonists (Enbrel, Humira)
- Patient must not have moderate to severe heart failure
- Cannot be used in combination with TNF antagonists or Kineret
|
| PEG-Intron (interferon alpha 2b)3 |
S0148 |
Pharmacy |
Hepatitis C Length of initial authorization: 3 months Length of continuation authorization: 3-9 months (dependent on genotype) |
- Diagnosis of chronic hepatitis C with liver disease
- No alcohol use within the past 6 months
- Cannot have decompensated liver disease
- Continued therapy will be approved if RNA titer is undetectable or < 100 times the original titer
|
| Prolastin (alpha 1 proteinase inhibitor) |
J0256 |
Medical |
Alpha-antitrypsin deficiency |
- Diagnosis of congenital alpha 1-antitrypsin deficiency
- Clinically evident emphysema
- FEV1 30-65% predicted
- Serum AAT level < 11mM/L (< 60 mg/dL)
|
| Prolia (denosumab) |
J0897 |
Medical |
Treatment of postmenopausal osteoporosis |
- Diagnosis of postmenopausal osteoporosis
- Documented therapeutic trial of alendronate (step 1) and Actonel (step 2)
|
| Provenge (sipuleucel-T)7 |
Q2043 |
Medical |
Treatment of advanced prostate cancer |
- Diagnosis of asymptomatic or minimally symptomatic metastatic castrate resistant (hormone refractory) prostate cancer
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-1
- Life expectancy greater than 6 months
- Serum prostate-specific antigen (PSA) ≥ 5 ng/mL
- Two sequential rising PSA levels obtained 2–3 weeks apart or other evidence of disease progression
- Serum testosterone < 50 ng/dL
- Prior use of docetaxel every 3 weeks and steroids (NCCN category 1 recommendation)
- Provenge will not be authorized for patients with any of the following:
- Requirement for systemic corticosteroid use
- Use of opioid analgesics for cancer-related pain
- Visceral metastases
- ECOG performance status ≥ 2
- Pathologic long-bone fractures
- Spinal cord compression
See PA form for Medicare |
| Qutenza (capsaicin 8% patch) |
J7335 |
Medical |
Post-herpetic neuralgia |
- Diagnosis of post-herpetic neuralgia
- Trial and failure of all of the following:
- Gabapentin
- Lyrica (requires step therapy with gabapentin)
- Generic tricyclic antidepressant (TCA)
- oxycodone CR or morphine CR
- Lidoderm Patch (requires prior authorization)
|
Click the drug name to get the PA form |
Code |
Benefit |
Use |
Criteria for coverage |
| Reclast (zoledronic acid)6 |
J3488 |
Medical |
Per 1 mg; treatment of osteoporosis Length of authorization: 2 years, given as 1 infusion per year |
- Diagnosis of Paget's disease or postmenopausal osteoporosis (T-score < -2.5)
- Documented trial and failure with both Fosamax (alendronate) and Actonel
|
Remicade (infliximab)7
|
J1745 |
Medical |
Per 10 mg; for treatment of rheumatoid arthritis, ankylosing spondylosis, Crohn's disease, ulcerative colitis, plaque psoriasis, psoriatic arthritis, or ankylosing spondylitis Length of initial authorization: 14 weeks Length of continuation authorization: 1 year (3 months for psoriasis)
|
- Diagnosis of rheumatoid arthritis, ankylosing spondylosis, Crohn's disease, ulcerative colitis, plaque psoriasis, psoriatic arthritis, or ankylosing spondylitis
- Negative TB test (provided on an annual basis)
- Rheumatoid arthritis requires treatment failure with steroids and methotrexate
- Crohn's disease requires treatment failure with two or more conventional therapies
- Ankylosing spondylitis requires BASDAI of at least 4, failure of at least 2 NSAIDs, intra-articular steroids, and sulfasalazine in patients with peripheral arthritis
- Psoriatic arthritis requires treatment failure with one or more DMARD
- Ulcerative colitis requires therapeutic trial of conventional therapy
- Plaque psoriasis affecting > 10% of BSA (unless hands, feet, head and neck, or genitalia) and a documented trial of one topical agent, one systemic treatment, and phototherapy
- The following indications require treatment failure with a self-injectable anti-TNF agent (e.g. Enbrel, Humira, Raptiva):
- Rheumatoid arthritis
- Psoriatic arthritis
- Plaque psoriasis
- Crohn's disease
- Ankylosing spondylitis
See PA form for Medicare |
| Remodulin (treprostinil sodium) |
J3285 |
Medical |
Per 1 mg; for treatment of pulmonary hypertension Length of initial authorization: 3 months Length of continuation authorization: 1 year |
- Diagnosis of pulmonary arterial hypertension
- Trial of Tracleer
- Trial of Flolan
- Completion of six-minute walk
|
| Rituxan (rituximab)5,7 |
J9310 |
Medical |
10mg/mL Length of initial authorization: 3 months Length of continuation authorization
|
- Treatment of Non-Hodgkins Lymphoma
- Treatment of CD20-expressing neoplasm (e.g. chronic lymphocytic leukemia, Waldenström macroglobulinemia, hairy cell leukemia, mantle cell lymphoma)
- Treatment of Thrombocytopenic purpura. One of the following is required:
- Patient did not respond to plasma exchange;
- Patient developed worsening disease in spite of continuing plasma exchange plus glucocorticoids;
- Patient has relapsing disease
- Treatment of Rheumatoid Arthritis. Requires one or more DMARDs AND prior use of self-injectable anti-TNF.
See PA form for Medicare |
| Simponi (golimumab) |
J3590 |
Pharmacy |
Treatment of Ankylosing spondylitis, Psoriatic arthritis and Rheumatoid arthritis |
Requires a trial and failure of preferred agents, Enbrel and Humira. (PA required for preferred agents) |
| Soliris (golimumab) |
J1300 |
Medical |
Treatment of paroxysmal nocturnal hemoglobinemia (PNH) |
- Diagnosis of paroxysmal nocturnal hemoglobinuria (PNH)
- Age ≥ 18 years
- At least four or more transfusions in the last 12 months
- Flow cytometric confirmation or at least 10% PNH cells
- Platelet counts at least 100,000/mm3
- Meningococcal vaccinated at least 2 weeks before treatment initiation
|
| Stelara (ustekinumab) |
J3357
|
Medical |
Treatment of moderate to severe plaque psoriasis
|
- Moderate to Severe Plaque Psoriasis (BSA ≥10%) who are candidates for phototherapy or systemic therapy.
- Patient age ≥ 18 years
- Documented therapeutic trial of at one self-injectable biologic agent (Enbrel, Humira)
- Trial of topical, systemic and phototherapy for at least 3 months.
- Negative TB test (must be done yearly)
- Patient cannot take in combination with other biologics (Enbrel, Humira, Cimzia, Simponi, Remicade, Kineret, Amevive)
|
| Synagis (palvizumab) |
90378
|
Medical |
Immune globulin for respiratory syncytial virus (RSV) Length of authorization: 5 infusions (given monthly November - March) |
See PA form for complete details coverage information |
| Teflaro (ceftaroline fosamil) |
J0712 |
Medical |
Medical Treatment of CABP and ABSSSI |
- Diagnosis of community-acquired bacterial pneumonia (CABP) requires trial and failure with ceftriaxone
- Diagnosis of acute bacterial skin and skin structure infection requires trial and failure with vancomycin
|
Click the drug name to get the PA form |
Code |
Benefit |
Use |
Criteria for coverage |
Tysabri (natalizumab)
|
J2323 |
Medical |
Per 1 mg; for treatment of multiple sclerosis Length of authorization: Indefinite |
- Diagnosis of relapsing-remitting form of multiple sclerosis
- > 18 years of age
- Previous use of Copaxone
- Previous use of Interferon product
|
Vectibix (panitumumab)6
|
J9303 |
Medical |
Treatment of advanced metastatic colorectal cancer Length of authorization: 4 injections
|
- Documented negative KRAS mutation status for colorectal cancer
- Previous treatment with fluoropyridimine-containing chemo, oxaliplatin-containing chemo, or irinotecan-containing chemo
|
Vibativ (telavancin)
|
C9399 J3490 |
Medical |
Treatment of complicated skin and skin structure infections |
- Diagnosis of suspected or confirmed MRSA
- Trial/failure with IV vancomycin (unless contraindicated)
|
| Xeomin (incobotulinumtoxin A)1 |
J0588 |
Medical |
Per unit, for various neuro-muscular uses: see PA form for covered conditions Length of authorization: 1 injection Injections must be separated by at least 90 days |
- See PA form for a list of covered indications
- Treatment for anal fissures and headache diagnoses require a clinical trial of conventional therapies
See PA form for Medicare |
| Xgeva (denosumab) |
J0897 |
Medical |
Treatment of metastatic breast and prostate cancer |
- Diagnosis of bone metastases.
- Documented therapeutic trial and clinical failure with Zometa® (not required if the patient has advanced breast or prostate cancer).
|
| Xiaflex (collagenase clostridium histolyticum) |
J0775 |
Medical |
Treatment of adult Dupuytren's contracture |
- Diagnosis of Dupuytren's contracture
- Flexion contracture of at least one finger, other than the thumb, of ≥ 20 degrees at the MP or PIP joints
- Patient is free of a chronic muscular, neurological, or neuromuscular disorder affecting the hands
- Patient is not a candidate for surgical palmar fasciotomy
|
Xolair (omalizumab)2,7
|
J2357 |
Medical or Pharmacy
|
Anti-IgE therapy for treating moderate to severe allergic asthma Length of initial authorization: 6 months Length of continuation authorization: 1 year |
- Diagnosis of allergic asthma requiring daily inhaled corticosteroids
- Compliant and persistent use of inhaled corticosteroids (75% adherence)
- Steroid dependency > 3 months, > 2 steroid bursts in last 12 months, or > 2 ED visits in last 12 months
- Positive perennial aeroallergen test
- IgE level 30-700 IU/ml
- > 12 years of age
- No tobacco use
See PA form for Medicare |
| Yervoy (ipilimumab) |
J9228 |
Medical |
Treatment of unresectable or metastatic melanoma |
- Diagnosis of unresectable or metastatic melanoma
- Agreement to permanently discontinue Yervoy if the patient experiences any severe adverse reactions
- Prescriber must communicate directly, face-to-face, with patient to provide both verbal and printed materials regarding the safety risks associated with the use of Yervoy.
|
| Zemaira (alpha 1 proteinase inhibitor) |
J0256
|
Medical |
Alpha-antitrypsin deficiency
|
- Diagnosis of congenital alpha 1-antitrypsin deficiency
- Clinically evident emphysema
- FEV1 30-65% predicted
- Serum AAT level < 11mM/L (< 60 mg/dL)
|
Zevalin (ibritumomab tiuxetan)
|
A9543 |
Medical |
Radioimmunotherapy; indicated for the treatment of relapsed or refractory low-grade, follicular, or transformed B-cell non-Hodgkin's lymphoma (NHL) |
- Diagnosis of relapsed or refractory low grade, follicular, or transformed B-cell non-Hodgkin's lymphoma or rituximab refractory follicular B-cell Hodgkin's lymphoma
- Platelet count > 100,000/mm3
- < 25% bone marrow involvement
- Neutrophil count > 1500/mm3
- Cannot have had prior myeloablative therapies with autologous bone marrow transplantation or peripheral stem cell collection
- Cannot have history of failed stem cell collection
- Cannot have history of prior external radiation to > 25% of active marrow
|
Zyvox IV
|
J2020
|
Medical |
2mg/mL in 100, 200, and 300ml single use bags
|
- Patient was started on Zyvox oral or IV in the hospital, or other inpatient setting and will be continuing therapy
- Patient has vancomycin-resistant Enterococcus faecium infection
- Patient has a documented methicillin-resistant staph aureus (MRSA) infection
See PA form for complete details |
back to top - No authorization required when Botulinum toxin is billed by neurologists, rehabilitation medicine or physical medicine.
- Once criteria are met, review for annual renewal of authorization. Documentation should not need to be submitted.
- Covered only with prescription benefit. Must be purchased through a specialty pharmacy.
- No authorization required when Euflexxa billed by orthopedic specialists, physiatrists, or rheumatologists.
- No authorization required for Rituxan for Non-Hodgkin's Lymphoma and other CD20-expressing neoplasm (e.g. chronic lymphocytic leukemia, Waldenström macroglobulinemia, hairy cell leukemia, mantle cell lymphoma).
- No authorization required for Medicare. Must use CPT code outlined in the CMS local coverage determination (LCD) available at www.cms.hhs.gov/mcd/search.asp?from2=search.asp&
- Priority Health Medicare applies CMS local coverage determination criteria when available for Part B drugs.
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