The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
127966911 12796691 1 I 20160919 20160929 20160929 EXP PHHY2016US132471 ALCON 26.00 YR F Y 0.00000 20160929 OT US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
127966911 12796691 1 PS DORZOLAMIDE/TIMOLOL SANDOZ DORZOLAMIDETIMOLOL 1 Unknown U 0
127966911 12796691 2 SS LATANOPROST. LATANOPROST 1 Unknown U 0
127966911 12796691 3 SS BRIMONIDINE BRIMONIDINE TARTRATE 1 Topical U 0
127966911 12796691 4 SS ACETAZOLAMIDE. ACETAZOLAMIDE 1 Oral U 0
127966911 12796691 5 C METHOTREXATE. METHOTREXATE 1 0
127966911 12796691 6 C TRIAMCINOLONE ACETATE TRIAMCINOLONE ACETONIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127966911 12796691 1 Intraocular pressure increased
127966911 12796691 2 Intraocular pressure increased
127966911 12796691 3 Intraocular pressure increased
127966911 12796691 4 Intraocular pressure increased
127966911 12796691 5 Uveitis
127966911 12796691 6 Uveitis

Outcome of event

Event ID CASEID OUTC COD
127966911 12796691 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127966911 12796691 Drug ineffective

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found