Ranibizumab
رانیبیزوماب
👁️ Sensory OrgansVEGF inhibitor (intravitreal)
Market / country: 🇺🇸 USA
Lucentis (US)
🧮 Dose calculator
Neovascular (wet) age-related macular degeneration · Regimen source: FDA Lucentis · 2.2
- • Ophthalmologist only. Less effective alternative: 3 monthly doses then less frequent with monitoring. FDA Lucentis · 2.2
Enter age (weight is optional for this regimen).
🛡️ Safety & information
Contraindications
- ⛔ Ocular or periocular infection; hypersensitivity to ranibizumab. FDA Lucentis · 4
Warnings
- • Endophthalmitis and retinal detachment after injection; raised intraocular pressure; arterial thromboembolic events. FDA Lucentis · 5
- • Retinal vasculitis. FDA Lucentis · 5.5
Formulations
- 0.5 mg (0.05 mL of 10 mg/mL) prefilled syringe — injection 🇺🇸 USA FDA Lucentis · 3
- 0.3 mg (0.05 mL of 6 mg/mL) prefilled syringe — injection 🇺🇸 USA FDA Lucentis · 3
👥 Special populations
- 🤰 PregnancyUse with caution
Label states no clear risk or has limited data; use only if needed, under medical advice. FDA Lucentis · 8.1
“Risk Summary There are no adequate and well-controlled studies of LUCENTIS administration in pregnant women.”
- 🤱 BreastfeedingUse with caution
Label: use with caution while breastfeeding; see the label text. FDA Lucentis · 8.2
“Because many drugs are excreted in human milk, and because the potential for absorption and harm to infant growth and development exists, caution should be exercised when LUCENTIS is administered to a nursing woman.”
- 👶 ChildrenSafety not established
Label: safety and effectiveness in children have not been established. FDA Lucentis · 8.4
“The safety and effectiveness of LUCENTIS in pediatric patients have not been established.”
- 👴 Older adultsUse with caution
Label: use with caution in older adults, usually starting at the low end of the dose range. FDA Lucentis · 8.5
“In the clinical studies, approximately 76% (2449 of 3227) of patients randomized to treatment with LUCENTIS were ≥ 65 years of age and approximately 51% (1644 of 3227) were ≥ 75 years of age [see Clinical Studies (14) ].”
- ⚥ Females & males of reproductive potentialUse with caution
Label has advice on pregnancy testing, contraception or fertility for females and males. FDA Lucentis · 8.3
“Based on the anti-VEGF mechanism of action for ranibizumab, treatment with LUCENTIS may pose a risk to reproductive capacity.”
🔗 Reference links
- FDA (approval record)BLA125156
- DailyMed (FDA label)FDA Lucentis
- MedlinePlus (NIH)Ranibizumab ImplantRanibizumab Injection
- WHO ATC/DDDS01LA04
- Darooyab (Iran)Ranibizumab
🇮🇷 Registered in Iran Darooyab · G-4793/Ranibizumab
Dosage forms with Iranian generic codes, per Darooyab.
- 19598 · RANIBIZUMAB 0.5MG/0.05ML 0.23ML VIAL · ویال رانیبیزومب ۰٫۵ میلیگرم / ۰٫۰۵ میلیلیتر ۰٫۲۳ میلیلیتر
- 11416 · RANIBIZUMAB 10MG/ML AMP · آمپول رانیبیزومب ۱۰ میلیگرم / میلیلیتر
📚 Reference status for this drug
Shows which sources have references recorded for this drug and which do not.
- FDA label (DailyMed)✅ PresentFDA Lucentis · 3FDA Lucentis · 2.2FDA Lucentis · 2.3FDA Lucentis · 2.4FDA Lucentis · 4FDA Lucentis · 5FDA Lucentis · 5.5FDA Lucentis · SPL approval / marketing categoryFDA Lucentis · 8.1FDA Lucentis · 8.2FDA Lucentis · 8.4FDA Lucentis · 8.5FDA Lucentis · 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-4793/Ranibizumab
- Clinical review⚠ Unverified