Humira® is covered for the following uses:
Requests for a non-FDA approved ("off-label") indication requires the proposed indication be listed in either the American Hospital Formulary System (AHFS), USP-DI, or Drugdex and is considered subject to evaluation of the prescriber's medical rationale, formulary alternatives, the available published evidence-based research and whether the proposed use is determined to be experimental/investigational.
NA
For Rheumatoid Arthritis must be prescribed by (or in consultation with) a rheumatologist.
For Chronic Plaque Psoriasis must be prescribed by (or in consultation with) a rheumatologist or dermatologist.
For initiation of treatment, a prior authorization form and relevant chart notes documenting medical rationale are required and for continuation of therapy, ongoing documentation of successful response to the medication may be necessary.
For Rheumatoid Arthritis the following additional criteria must be met:
For Chronic Plaque Psoriasis the following additional criteria must be met:
For Crohn's Disease the following additional criteria must be met:
For all diagnoses, dosing must be consistent with labeling.
For reauthorization, documentation of adequate response to the medication must be provided.
NA:
Initial authorization will be for up to six months. Reauthorization will be for up to one year.