
Actemra400 mg/20
Roche Bangladesh Ltd.
Tocilizumab is a recombinant humanized monoclonal antibody that blocks the interleukin-6 (IL-6) receptor.
Tocilizumab is a recombinant humanized monoclonal antibody that blocks the interleukin-6 (IL-6) receptor. It is used for the following indications:
Because Tocilizumab is a biologic agent with a boxed warning for serious infection, it should be prescribed and monitored only by a physician experienced in its use.
Tocilizumab dosing depends on the indication, route of administration (intravenous or subcutaneous), and patient body weight. Treatment should be initiated and supervised by a physician experienced in diagnosing and treating the relevant condition.
| Indication | Route | Dose |
|---|---|---|
| Rheumatoid arthritis (adult) | IV infusion | 4 mg/kg every 4 weeks, may increase to 8 mg/kg based on clinical response (max 800 mg/infusion); infused over 60 minutes |
| Rheumatoid arthritis (adult) | Subcutaneous | 162 mg once weekly (body weight ≥100 kg) or once every other week (body weight <100 kg), adjusted by response |
| Giant cell arteritis (adult) | Subcutaneous | 162 mg once weekly, typically with a tapering glucocorticoid course |
| Polyarticular JIA (≥2 yrs) | IV infusion | Weight-based: 10 mg/kg (<30 kg) or 8 mg/kg (≥30 kg) every 4 weeks |
| Systemic JIA (≥2 yrs) | IV infusion | Weight-based: 12 mg/kg (<30 kg) or 8 mg/kg (≥30 kg) every 2 weeks |
| Cytokine release syndrome (≥2 yrs) | IV infusion | 8 mg/kg (≥30 kg) or 12 mg/kg (<30 kg) as a single dose, infused over 1 hour; up to 3 additional doses may be given if inadequate response, at least 8 hours apart (max 4 doses total) |
| COVID-19 (hospitalized, ≥2 yrs) | IV infusion | 8 mg/kg (≥30 kg) or 12 mg/kg (<30 kg) as a single dose (max 800 mg); a second dose may be given if clinical signs/symptoms worsen or fail to improve, at least 8 hours after the first |
Doses should be administered by a healthcare professional. Baseline and periodic laboratory monitoring (complete blood count, liver function tests, lipid profile) is required before and during treatment, and dose adjustments or temporary interruption may be needed based on laboratory abnormalities. See Precautions and Warnings for monitoring requirements.
The most commonly reported adverse effects of Tocilizumab (occurring in ≥5% of patients) include:
Tocilizumab is contraindicated in patients with:
Disclaimer
The information provided is accurate to the best of our knowledge, but it does not replace professional medical advice. We cannot guarantee its completeness or accuracy, and the absence of specific information about a drug should not be taken as an endorsement. We are not responsible for any consequences arising from this information, so please consult a healthcare professional for any concerns or questions.