FDA Adverse Event Injury Summary report: N

CEEON

MDR report key: 401659 · Received June 21, 2002

Report

Report Number
9614546-2002-00019
Event Type
Injury
Date Received
June 21, 2002
Report Date
June 21, 2002
Manufacturer
PHARMACIA & UPJOHN GRONINGEN
Product Code
HQL
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

MALPOSITIONED INTRAOCULAR LENSES [LENS DISLOCATION]. UVEITIS [UVEITIS NOS]. GLAUCOMA [GLAUCOMA NOS]. HYPHEMA [HYPHAEMA]. CASE DESCRIPTION: SPONTANEOUS LITERATURE, LOCAL REF. N. 02-00468, ARGUS N. 2002111387US. A LITERATURE PAPER (AM.J.OPHTHALMOL; 133(6);839-41;2002) REPORTED A CASE REGARDING A PT WHO UNDERWENT A LENS IMPLANTATION FOR CATARACT EXTRACTION ON UNK DATE. SIX YEARS AFTER THE SURGICAL INTERVENTION, THE PT DEVELOPED UVEITIS-GLAUCOMA-HYPHEMA SYNDROME OF THE RIGHT EYE. UVEITIS-GLAUCOMA-HYPHEMA SYNDROME CAN LEAD TO LOSS OF VISION FROM GLAUCOMATOUS OPTIC NEUROPATHY, CHRONIC INFLAMMATION, CYSTOID MACULAR EDEMA, AND INTRAOCULAR HEMORRHAGE. SURGICAL INTERVENTION IS OFTEN REQUIRED TO RESTORE NORMAL INTRAOCULAR ANATOMY, REPLACE POORLY POSITIONED INTRAOCULAR LENSES, OR CONTROL GLAUCOMA. AN ULTRASOUND BIOMICROSCOPY, REVEALED A LENS MALPOSITION, IN WHICH BOTH THE HAPTICS ERODED INTO THE CILIARY BODY. THE OUTCOME IS UNK.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CEEON INTRAOCULAR LENS HQL PHARMACIA & UPJOHN GRONINGEN 912 UNK

Patients

Seq Age Sex Outcome Treatment
1 79 YR Required Intervention| S