Actemra Injection

Actemra Injection

S4
PDF Leaflet Revision Date: 26 May 2023

API: Tocilizumab | Company: Roche Products

Clinical Summary

Quick overview from the medicine insert

Indication

Treatment of severe rheumatoid arthritis and juvenile idiopathic arthritis.

Dosage (summary)

RA: 8 mg/kg IV every 4 weeks; pJIA: 10 mg/kg (<30 kg) or 8 mg/kg (u226530 kg) IV every 4 weeks; sJIA: 12 mg/kg (<30 kg) or 8 mg/kg (u226530 kg) IV every 2 weeks.

Onset of Action / Duration

Onset: 6-12 weeks for clinical improvement.

Special Populations

  • Children
  • Elderly
  • Renal impairment
  • Hepatic impairment

Pregnancy & Breastfeeding

Not recommended in pregnancy; unknown if excreted in breast milk.

Key Drug Interactions

  • MTX
  • CYP450 substrates
  • TNF antagonists

Contraindications

  • Hypersensitivity to tocilizumab
  • Active severe infections

Common side effects

  • Upper respiratory tract infections
  • Headache
  • Hypertension
  • Increased ALT

Counselling Points

  • Monitor for infections
  • Avoid live vaccines
  • Report any allergic reactions
  • Regular lab monitoring for liver and blood counts

Serious warnings

  • Serious infections
  • Gastrointestinal perforation
  • Hypersensitivity reactions
  • Liver enzyme elevations
Important Disclaimer

The Actemra Injection professional information leaflet below is the property of Roche Products and is provided on Medinsert exactly as issued, with no.. alterations or editorial changes. We make every effort to keep content current by updating documents as soon as new versions become available. Medinsert serves as a trusted access point for healthcare professionals, but does not replace official sources or clinical judgement. For more details, please read our full disclaimer. read more>>

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