
Lucentis0.5 mg/0.0
Novartis (Bangladesh) Ltd.
Ranibizumab is a vascular endothelial growth factor (VEGF) inhibitor administered by intravitreal injection.
Ranibizumab is a vascular endothelial growth factor (VEGF) inhibitor administered by intravitreal injection. Its indications, classified by strength of evidence, are:
Ranibizumab is used only for these retinal/ocular vascular conditions; it has no approved systemic (oral/IV) indication.
Ranibizumab must be administered only by a qualified ophthalmologist experienced in intravitreal injections, under aseptic (sterile) conditions, typically in a controlled clinical setting with appropriate anesthesia and periocular antisepsis.
| Indication | Typical adult dose | Frequency |
|---|---|---|
| Wet AMD | 0.5 mg (0.05 mL) intravitreally | Monthly; may be extended after initial loading doses based on response, with regular monitoring |
| Diabetic macular edema (DME) / diabetic retinopathy | 0.5 mg (0.05 mL) intravitreally | Monthly, per physician assessment |
| Macular edema after RVO | 0.5 mg (0.05 mL) intravitreally | Monthly |
| Myopic choroidal neovascularization | 0.5 mg (0.05 mL) intravitreally | Monthly, generally up to 3 initial doses, then as needed |
| Retinopathy of prematurity (pediatric) | 0.2 mg (0.02 mL) per eye | Single dose per eye, repeat only per specialist assessment |
The exact dosing interval and duration are individualized by the treating ophthalmologist based on visual acuity, anatomical response (e.g. optical coherence tomography findings), and disease activity. See Dosage and Administration sections below for further detail; see Precautions and Warnings for injection-related risks.
Side effects of Ranibizumab may relate either to the intravitreal injection procedure itself or to the drug's pharmacological effect.
Patients should seek urgent ophthalmologic review for eye pain, redness, light sensitivity, or sudden vision changes after a Ranibizumab injection.
Ranibizumab is contraindicated in patients with:
These are true absolute contraindications; other concerns such as thromboembolic risk or intraocular pressure changes are precautions rather than contraindications and are discussed in Precautions and Warnings.
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.