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
126791931 12679193 1 I 20160816 20160824 20160824 EXP BR-PFIZER INC-2016392214 PFIZER 60.00 YR F Y 62.00000 KG 20160824 CN BR BR

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
126791931 12679193 1 PS XALATAN LATANOPROST 1 Ophthalmic UNK L51597L44855 20597 EYE DROPS, SOLUTION
126791931 12679193 2 SS GLAUB BRIMONIDINE TARTRATE 1 Ophthalmic UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126791931 12679193 1 Glaucoma
126791931 12679193 2 Glaucoma

Outcome of event

Event ID CASEID OUTC COD
126791931 12679193 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126791931 12679193 Cataract
126791931 12679193 Diabetes mellitus

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
126791931 12679193 1 201511 0
126791931 12679193 2 201510 20160803 0