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
96820431 9682043 1 I 20130621 20131030 20131111 20131111 EXP ALCN2013FR005589 ALCON 73.00 YR M Y 0.00000 20131111 OT FR FR

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
96820431 9682043 1 PS IOPIDINE 1 OPHTHALMIC UNK Y 20258 EYE DROPS
96820431 9682043 2 SS IOPIDINE 1 OPHTHALMIC UNK Y 20258 EYE DROPS
96820431 9682043 3 SS ACULAR 1 OPHTHALMIC UNK Y 0
96820431 9682043 4 SS ACULAR 1 UNK Y 0
96820431 9682043 5 SS MYDRIATICUM 1 OPHTHALMIC UNK D 0
96820431 9682043 6 SS NEOSYNEPHRINE 1 OPHTHALMIC UNK D 0 EYE DROPS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
96820431 9682043 1 Preoperative care
96820431 9682043 2 Postoperative care
96820431 9682043 3 Preoperative care
96820431 9682043 4 Postoperative care
96820431 9682043 5 Preoperative care
96820431 9682043 6 Preoperative care

Outcome of event

Event ID CASEID OUTC COD
96820431 9682043 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
96820431 9682043 Condition aggravated
96820431 9682043 Muscular weakness

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
96820431 9682043 1 20130619 0
96820431 9682043 2 20130724 0
96820431 9682043 3 20130619 0
96820431 9682043 4 20130724 0
96820431 9682043 5 20130619 0
96820431 9682043 6 20130619 0