adalimumab
Drug Name | Form | Strength | Formulary Unrestricted | Formulary Restricted | Non-Formulary | Interchange |
---|---|---|---|---|---|---|
Hulio (adalimumab-fkjp) | DEVICE, SUBCUTANEOUS | 40 mg/0.8 mL, 20 mg/0.4 mL | ||||
Abrilada (adalimumab-afzb) | INJECTION, SUBCUTANEOUS | 10 mg/0.2 mL, 20 mg/0.4 mL, 40 mg/0.8 mL | ||||
Amjevita (adalimumab-atto) | INJECTION, SUBCUTANEOUS | 20 mg/0.4 mL, 40 mg/0.8 mL | ||||
Cyltezo (adalimumab-adbm) | INJECTION, SUBCUTANEOUS | 40 mg/0.8 mL | ||||
Hadlima (adalimumab-bwwd) | INJECTION, SUBCUTANEOUS | 40 mg/0.8 mL | ||||
Hyrimoz (adalimumab-adaz) | INJECTION, SUBCUTANEOUS | 40 mg/0.8 mL | ||||
Idacio | INJECTION, SUBCUTANEOUS | 40 mg/0.8 mL | ||||
Yusimry (adalimumab-aqvh) | INJECTION, SUBCUTANEOUS | 40 mg/0.8 mL | ||||
Humira Pen | KIT, SUBCUTANEOUS | 40 mg/0.8 mL, 80 mg/0.8 mL |
Humira medication guide
All biosimilars were classified as therapeutically equivalent to Humira and other adalimumab biosimilars for all FDA approved indications if need arises in adult patients.
Inpatients may use home supply.
As of May 2022, the HUMIRA First Dose Program (a no cost loading dose) has been discontinued by the manufacturer.
If the loading dose is ordered, the pharmacist should contact the prescriber and inform them that the program has been discontinued.
Dose administration should be deferred until after discharge.
Reviewed: March 25, 2014 (IBD loading dose), January 2022 (Biosimilars), April 2023 (Idacio), September 2023 (Yusimry)
Update: May 2022 (First Dose Program Discontinued)
Spotlight Adalimumab-aacf (Idacio)
Adalimumab-aqvh (Yusimry)