RETISERT Safety Questions, RETISERT Answers
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RETISERT Safety Reports
Total RETISERT reports: 4.RETISERT FDA safety alerts: No.
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Physician from UNITED STATES reported RETISERT problem on Jan 31, 2007. Male patient, 65 years of age, was diagnosed with uveitis and was treated with RETISERT. After drug was administered, patient experienced the following problems/side effects: cytomegalovirus chorioretinitis, macular oedema, vitritis. RETISERT dosage: unknown. Patient recovered.
RETISERT problem was reported by a Physician from UNITED STATES on Nov 16, 2006. Female patient, 57 years of age, was diagnosed with uveitis, vasculitis and was treated with RETISERT. After drug was administered, patient experienced the following problems/side effects: hypotony of eye. RETISERT dosage: unknown. During the same period patient was treated with PREDTE, CYCLOSPORINE, HYDROCHLOROTHIAZIDE, SYNTHROID, SCOPOLAMINE. Patient recovered.
Consumer or non-health professional from UNITED STATES reported RETISERT problem on Apr 03, 2006. Male patient, 47 years of age, was diagnosed with uveitis and was treated with RETISERT. After drug was administered, patient experienced the following problems/side effects: eye inflammation, eye swelling, intraocular pressure decreased, vision blurred, vitreous floaters. RETISERT dosage: unknown. During the same period patient was treated with PREDTE, ATROPINE. Patient recovered.
RETISERT problem was reported by a Physician from UNITED STATES on Nov 15, 2006. Female patient, 42 years of age, was diagnosed with choroiditis and was treated with RETISERT. After drug was administered, patient experienced the following problems/side effects: activities of daily living impaired, choroidal effusion, corneal oedema, device dislocation, eye disorder, eye haemorrhage, eye inflammation, eye pain. RETISERT dosage: 0.59 MILLIGRAMS; RIGHT EYE. Patient recovered.