Beovu

Active Ingredient(s): Brolucizumab-dbll
FDA Approved: * October 7, 2019
Pharm Company: * NOVARTIS PHARMS CORP
Category: Vision / Eye Health

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".



Beovu Overview

Brolucizumab, sold under the trade name Beovu, is a humanized single-chain antibody fragment for the treatment of neovascular (wet) age-related macular degeneration (AMD).[3][4] The most common side effects are reduced visual acuity, cataract (clouding of the lens in the eye), conjunctival haemorrhage (bleeding at the front of the eye) and vitreous floaters (spots in the vision).[3][4] The most serious side effects are blindness,...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Brolucizumab

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Possible Dosages for this and Related Drugs:

Brolucizumab-dbll
  • Injection: 6mg/0.05ml
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Beovu: (1 result)

Sorted by National Drug Code
  • 0078-0827 Beovu 6 mg/.05ml Intravitreal Injection, Solution by Novartis Pharmaceuticals Corporation

Other drugs which contain Brolucizumab-dbll or a similar ingredient: (1 result)




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