Below are a list of core therapy drugs we provide and a list of potential diagnoses that they may treat.
Core Neuro Therapies:
Neuro Diagnoses
- IVIG
- Gamunex-C J1561
- Pribigen J1459
- Gammagard J1569
- Octagam J1568
- Gammaked J1561
- Lemtrada (alemtuzumab) J0202
- Lumizyme (algucosidase alfa) J0221
- Ocrevus (ocrelizumab) J2350
- Onpattro (patisiran) J0222
- Radicava (edaravone) J1301
- Rituxan (rituximab J9312 (Truxima Q5115 & Ruxience Q5119)
- Soliris (eculizumab) J1300
- Tysabri (natalizumab) J2323
- Uplina (inebilizumab-cdon) J1823
- Vyepti (eptinezumab-jjmr) J3021
- ALS
- CIDP (Chronic INflammatory Demyelinating Polyneuropathy)
- hATTR (Heriditary transthyretin-mediated amyloidosis)
- Migraines
- MS
- Myasthenia Gravis
- NMOSD (Neuromyelitis Optica Spectrum Disorder)
- Pompe Disease
Core Rheumatology Therapies:
- Actemra (tocolizumab) J3262
- Benlysta (belimuab) J0490
- Boniva (ibandronate) J1740
- Cimiza (certolizumab pego) J0717
- Evenity (romosuzmab-aqqg) J311
- Krystexxa (pegloticase) J2507
- Orencia (abatacept) J0129
- Prolia (denosumab) J0897
- Reclast (zoletronic acid) J3489
- Remicade (infliximab) J1745 (Inflectra Q5103, Renflexis Q5104 & Avsola Q5121)
- Rituxan (ritumimab) J8312 (Truxima Q5115 & Ruxience !5119)
- Simponi Aria (golimumab) J1602
- Stelara (ustekinumab) J3358
- Tepezza (teprotumumab-trbw) J3241
Rheumatology Diagnoses:
- Ankylosing Spondylitis
- Gout
- Microscopic Polyangiitis (MPA)
- Osteoporosis
- Paget’s Diesase
- Plaque Psoriasis
- Psoriatic arthritis
- Rheumatoid arthritis (RA)
- Systemic Lupus Erythematosus
- Thyroid Eye Disease
- Wegener’s Disease (GPA)
Core GI Therapies:
- Cimizia (certolizumab pego) J0717
- Entyvio (vedolisumab) J3380
- Remicade (infliximab) J1745 (Inflectra Q5103, Renflexis Q5104 & Avsola Q5121)
- Stelara (ustekinumab) J3358
- Tysabri (natalizumab) J2323
GI Diagnoses:
- Crohn’s Disease
- Ulcerative colitis
Core Immunodeficiency Therapies:
- Asceniv
- Octagam
Immunodeficiency Diagnoses:
- Common Variable Immunodeficiency (CVID)
- Congenital agammaglobulinemia
- Hypogammaglobulinemia
- Primary Humoral Immunodeficiency (PI)
- Severe Combined Immunodeficiency (SCID)
- Wiskott-Aldritch Syndrome
- X-inked agammaglobulinemia (XLI)
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