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Actemra - labeled renal guidance
Product / population
Tocilizumab (Actemra), IV / subcutaneous injection
Renal method
Renal impairment categories as defined by the cited product label
DailyMed / product prescribing information · Tocilizumab (Actemra), IV / subcutaneous injection
Renal method: Renal impairment categories as defined by the cited product label Source date: DailyMed SPL version 53, posted Dec 19, 2025 Retrieved: 2026-11-07
Qualified no-adjustment statement. Apply only to the population, product and renal range described in this source.
No renal dose change is required in mild or moderate impairment. Severe impairment has not been studied. Choose IV or subcutaneous dosing according to the indication and product presentation.
This reference does not select a regimen. Complete the indication, measured/estimated renal function and trend, dialysis setting, source rationale, monitoring and reassessment plan in your institution's approved documentation system. Confirm the complete current source before adopting its regimen.
GlobalRPh Renal Dosing Master v7.4. Review the retrieval and revision dates attached to each source. Selecting a reference does not imply clinical verification.
