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Procysbi

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https://www.readbyqxmd.com/read/25560059/cystinosis-a-new-perspective
#1
Koenraad R P Veys, Martine T P Besouw, Anne-Marie Pinxten, Maria Van Dyck, Ingele Casteels, Elena N Levtchenko
Cystinosis is a rare, autosomal recessive inherited lysosomal storage disease. It is the most frequent and potentially treatable cause of the inherited renal Fanconi syndrome. If left untreated, renal function rapidly deteriorates towards end-stage renal disease by the end of the first decade of life. Due to its rarity and non-specific presentation, the entity is often not promptly recognized resulting in delayed diagnosis. Two major milestones in cystinosis management, cystine-depleting therapy with cysteamine and renal allograft transplantation, have had a considerable impact on the natural history and prognosis of cystinosis patients...
June 2016: Acta Clinica Belgica
https://www.readbyqxmd.com/read/23946626/pharmaceutical-approval-update
#2
Marvin M Goldenberg
Extended-release carbinoxamine maleate oral suspension (Karbinaler) for allergicrhinitis; brinzolamide 1.0%/brimonidine tartrate 0.2% ophthalmic suspension (simbrinza) for open-angle glaucoma and ocular hypertension; and cysteamine bitartrate (Procysbi) for nephropathic cystinosis.
June 2013: P & T: a Peer-reviewed Journal for Formulary Management
https://www.readbyqxmd.com/read/23936975/do-comparable-efficacy-convenient-dosing-justify-procysbi-s-extremely-high-price
#3
Thomas Morrow
No abstract text is available yet for this article.
July 2013: Managed Care
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