Medicine guide

RANIVISIO

As listed in the register: RANIVISIO 10 mg/mL, solution injectable

10 mg · solution injectable

  • Prescription only
Active substance
Ranibizumab
Made by
MIDAS PHARMA (ALLEMAGNE)

Quoted from the official source. Not yet reviewed by Mediclarum — the leaflet in your pack is authoritative.

What it is for

Mediclarum has not yet retrieved and stored the official label for this product, so none of its text is shown here. Open the official leaflet

How it works

From the US prescribing label for the same active substance (LUCENTIS). It describes the substance, not this exact product.

Ranibizumab binds to the receptor binding site of active forms of VEGF-A, including the biologically active, cleaved form of this molecule, VEGF 110.

VEGF-A has been shown to cause neovascularization and leakage in models of ocular angiogenesis and vascular occlusion and is thought to contribute to pathophysiology of neovascular AMD, mCNV, DR, DME and macular edema following RVO.

Peak level after1 day
Half-life9 days
Mostly cleared after≈ 6 weeksfive half-lives — our arithmetic
PeakHalf gone6 weeks0
The shape is a standard model drawn from the two times above, not a measurement. How fast a medicine acts and wears off also depends on the dose, the form and the person.

Quoted from the prescribing label, sections “Mechanism of Action” and “Pharmacokinetics”. DailyMed · 2025-11-21

Safety of the active substance

From the US prescribing label for the same active substance (LUCENTIS). It describes the substance, not this exact product.

Must not be used by
  • Ocular or periocular infections ( 4.1 ) Hypersensitivity ( 4.2 ) 4.1 Ocular or Periocular Infections LUCENTIS is contraindicated in patients with ocular or periocular infections. 4.2 Hypersensitivity LUCENTIS is contraindicated in patients with known hypersensitivity to ranibizumab or any of the excipients in LUCENTIS.
  • Hypersensitivity reactions may manifest as severe intraocular inflammation.

Quoted from the US prescribing label for the same active substance. Your own pack’s leaflet is the authority for your product. DailyMed

Same active substance, strength and form in other countries

Matched on active substance, strength and kind of form only. This is not a statement that the products are equivalent or interchangeable: other ingredients, release and approved uses can differ — ask a pharmacist before swapping.

Medicine passport: one printable page to show a pharmacist abroad

European UnionNo exact match for this strength and form

CanadaNo exact match for this strength and form

Details

Made byMIDAS PHARMA (ALLEMAGNE)
Active substanceRanibizumab
Strength10 mg
Formsolution injectable
Routeintravitréenne
Dispensing (as stated by the register)prescription réservée aux spécialistes et services OPHTALMOLOGIE · liste I
MarketedYes, according to the register
Reinforced monitoringYes — under reinforced monitoring, according to the register
Authorisation procedureProcédure centralisée
EU numberEU/1/22/1673
Name in the registerRANIVISIO 10 mg/mL, solution injectable
Packs1 flacon(s) en verre de 0,23 ml
CIS64389258
CIP133400930258675

Source: Base de données publique des médicaments · 2026-09-30 · not reviewed by a clinician

Source : Base de données publique des médicaments (ANSM / Ministère de la Santé), sous Licence Ouverte. Reuse terms: Licence Ouverte / Open Licence (Etalab).

Other strengths and forms

2 products are sold under this name. Grouped by form; a number on a strength means several companies make it.

Same active substance

These contain the same substance. That does not mean one can replace another — ask a pharmacist.