Rituximab
ریتوکسیمب
🎗️ Antineoplastic And Immunomodulating AgentsAnti-CD20 antibody
Market / country: 🇺🇸 USA
Rituxan (US)
🧮 Dose calculator
B-cell non-Hodgkin lymphoma and CLL · Regimen source: FDA Rituxan · 2.2
- • Premedicate before each infusion: acetaminophen and an antihistamine (and steroid per regimen). IV infusion only, never push or bolus. FDA Rituxan · 2.8FDA Rituxan · 2.1
- • Relapsed/refractory: weekly for 4 or 8 doses; untreated: day 1 of each chemo cycle up to 8 doses. CLL: cycle 1 → 375, cycles 2–6 → 500 mg/m². FDA Rituxan · 2.2FDA Rituxan · 2.3
Enter age and weight.
🛡️ Safety & information
Warnings
- • Boxed warning: fatal infusion reactions (mostly the first), severe mucocutaneous reactions, hepatitis B reactivation (screen HBsAg and anti-HBc first), PML. FDA Rituxan · Boxed Warning
Formulations
- 10 mg/mL (100 mg/10 mL, 500 mg/50 mL vials) — injection 🇺🇸 USA FDA Rituxan · 3
👥 Special populations
- 🤰 PregnancyUse with caution
Label states no clear risk or has limited data; use only if needed, under medical advice. FDA Rituxan · 8.1
“Risk Summary Based on human data, RITUXAN can cause adverse developmental outcomes including B-cell lymphocytopenia in infants exposed to RITUXAN in-utero ( see Clinical Considerations ).”
- 🤱 BreastfeedingDangerous / avoid
Label: breastfeeding not recommended, or choose between the drug and breastfeeding. FDA Rituxan · 8.2
“Given that the clinical significance of this finding for children is not known, advise women not to breastfeed during treatment with RITUXAN and for 6 months after the last dose due to the potential of serious adverse reactions in breastfed children.”
- 👶 ChildrenUse with caution
The label has conditions, age limits or notes for children; the label sentence is quoted below. FDA Rituxan · 8.4
“Mature B-Cell NHL/B-AL The safety and effectiveness of RITUXAN in combination with chemotherapy for the treatment of previously untreated, advanced stage, CD20-positive DLBCL/BL/BLL/B-AL have been established in pediatric patients aged 6 months and older.”
- 👴 Older adultsUse with caution
Label: use with caution in older adults, usually starting at the low end of the dose range. FDA Rituxan · 8.5
“Patients 70 years or older received lower dose intensity of fludarabine and cyclophosphamide compared to younger patients, regardless of the addition of RITUXAN.”
- ⚥ Females & males of reproductive potentialUse with caution
Label has advice on pregnancy testing, contraception or fertility for females and males. FDA Rituxan · 8.3
“Contraception Females Advise females of reproductive potential to use effective contraception during treatment with RITUXAN and for 12 months after the last dose.”
🔗 Reference links
- FDA (approval record)BLA103705
- DailyMed (FDA label)FDA Rituxan
- MedlinePlus (NIH)Rituximab Injection
- WHO ATC/DDDL01FA01
- Darooyab (Iran)Rituximab
🇮🇷 Registered in Iran Darooyab · G-1062/Rituximab
Dosage forms with Iranian generic codes, per Darooyab.
- 02473 · RITUXIMAB 100MG/10ML VIAL · ویال ریتوکسیمب ۱۰۰ میلیگرم / ۱۰ میلیلیتر
- 02474 · RITUXIMAB 500MG/50ML VIAL · ویال ریتوکسیمب ۵۰۰ میلیگرم / ۵۰ میلیلیتر
- 52048 · RITUXIMAB INJECTION PARENTERAL 120 mg/1mL 11.7 mL · فرآورده تزریقی ریتوکسیمب ۱۲۰ میلیگرم / ۱ میلیلیتر ۱۱٫۷ میلیلیتر
- 52049 · RITUXIMAB INJECTION PARENTERAL 120 mg/1mL 13.4 mL · فرآورده تزریقی ریتوکسیمب ۱۲۰ میلیگرم / ۱ میلیلیتر ۱۳٫۴ میلیلیتر
📚 Reference status for this drug
Shows which sources have references recorded for this drug and which do not.
- FDA label (DailyMed)✅ PresentFDA Rituxan · 3FDA Rituxan · 2.2FDA Rituxan · 2.8FDA Rituxan · 2.1FDA Rituxan · 2.3FDA Rituxan · 2.5FDA Rituxan · 2.7FDA Rituxan · Boxed WarningFDA Rituxan · SPL approval / marketing categoryFDA Rituxan · 8.1FDA Rituxan · 8.2FDA Rituxan · 8.4FDA Rituxan · 8.5FDA Rituxan · 8.3
- UK SmPC (eMC / MHRA)❌ Not present
- Published guideline❌ Not present
- Licensed reference (medical school)❌ Not present
- Iranian leaflet (IFDA)❌ Not present
- Pharmacy website (secondary, unreliable)✅ PresentDarooyab · G-1062/Rituximab
- Clinical review⚠ Unverified