Actemra (Tocilizumab) 162mg ACTPen SC Prefilled AutoInjector

$1,300.00

Drug Info: ApoThera Drug Disease Clinical Support App

Rheumatoid Arthritis
Weight <100 kg
– 162 mg SC every other week
– Followed by an increase to every week based on clinical response
Weight ≥100 kg
– 162 mg SC every week
Transition from IV to SC
– Administer first SC dose instead of the next scheduled IV dose
Giant Cell Arteritis
Initial Dose
– 162 mg SC once weekly in combination with a tapering course of glucocorticoids
Maintenance Dose
– Based on clinical considerations, may consider administering 162 mg SC every other week in combination with a tapering course of glucocorticoids
Cytokine Release Syndrome (CRS)
Initial Dose
– 8 mg/kg IV infusion over 60 min
– SC is not approved for CRS
Maintenance Dose
– May administer up to 3 additional doses of tocilizumab if no clinical improvement in signs/symptoms of CRS after first dose
– Interval between consecutive doses should be >8 hr
– May be administered as monotherapy or with corticosteroids
Maximum Dose
– 800 mg/dose
COVID-19 (Adjunct Therapy)
Initial Dose
– 8 mg/kg IV infusion over 60 min
Maintenance Dose
– May administer up to 3 additional doses of tocilizumab if no clinical improvement in signs/symptoms of CRS after first dose
Find a Physician:
NDC: 50242-0143-01 Category:

2 Syringes = 1 Unit

Description

Drug Info: ApoThera Drug Disease Clinical Support App

Actemra Instructions for Use

SC Administration
– Administer the full amount in the prefilled syringe
– Allow to reach room temperature prior to use
– Do not use if particulate matter or discoloration is visible; solution should be clear and colorless to pale yellow
– Rotate injection sites; avoid injecting into moles, scars, or tender, bruised, red, or hard skin.
– Prefilled syringe is available for use by patients (self-administration).
 
Storage
– Store intact syringes at 2°C to 8°C (36°F to 46°F).
– Do not freeze.
– Protect vials and syringes from light (store in the original package until time of use)
– Keep syringes dry
 
Monitoring
– Latent TB screening prior to therapy initiation (all patients)
– Neutrophils, platelets, ALT/AST (prior to therapy, 4 to 8 weeks after start of therapy, and every 3 months thereafter [rheumatoid arthritis])
– Neutrophils, platelets, ALT/AST (prior to therapy, at second infusion, and every 2 to 4 weeks [systemic juvenile idiopathic arthritis] or 4 to 8 weeks [polyarticular juvenile idiopathic arthritis] thereafter)
– Additional liver function tests (bilirubin) as clinically indicated
– Lipid panel (prior to, at 4 to 8 weeks following initiation, and approximately every 6 months during therapy)
– Monitor all patients for signs and symptoms of infection (prior to, during, and after therapy)
– Signs and symptoms of CNS demyelinating disorders