The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6552556 7573280 I 6552556-0 20091218 20100106 20100121 EXP US-1180316 ALCON LABORATORIES, INC. 87 YR M N 20100118 OT UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6552556 1013003401 PS BSS 1 INTRAOCULAR (500 ML INTRAOCULAR), (15 ML INTRAOCULAR) D D 20742
6552556 1013068223 C VIGAMOX 1
6552556 1013068250 C OMNIPRED 1
6552556 1013068267 C VANCOMYCIN 1
6552556 1013068270 C CEFTAZIDIME 1
6552556 1013068273 C VISCOAT 2
6552556 1013068274 C PROVISC 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6552556 1013003401 INTRAOCULAR LENS IMPLANT

Outcome of event

Event ID OUTC COD
6552556 OT

Reactions reported

Event ID PT
6552556 POST PROCEDURAL COMPLICATION
6552556 TOXIC ANTERIOR SEGMENT SYNDROME

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

Event ID RPSR COD
6552556 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6552556 1013003401 20091217 20091217
6552556 1013003401 20091217 20091217