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
125573642 12557364 2 F 2012 20160714 20160714 20160726 EXP BR-PFIZER INC-2016328440 PFIZER 76.00 YR F Y 48.00000 KG 20160726 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
125573642 12557364 1 PS XALATAN LATANOPROST 1 Ophthalmic 1 DROP EACH EYE TWICE A DAY 20597 2 GTT EYE DROPS, SOLUTION BID
125573642 12557364 2 SS XALATAN LATANOPROST 1 Ophthalmic 3 DROPS IN EACH EYE, 3X/DAY 20597 6 GTT EYE DROPS, SOLUTION TID
125573642 12557364 3 C HYABAK 2 Ophthalmic 1 DROP EACH EYE, TWICE A DAY 0 BID
125573642 12557364 4 C VISCOTEARS CARBOMER 1 UNK 0
125573642 12557364 5 C LUT 2 UNK 0
125573642 12557364 6 C SOMALGIN ASPIRINDIHYDROXYALUMINUM AMINOACETATE ANHYDROUSMAGNESIUM CARBONATE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125573642 12557364 1 Eye disorder
125573642 12557364 3 Lacrimal disorder

Outcome of event

Event ID CASEID OUTC COD
125573642 12557364 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125573642 12557364 Drug prescribing error
125573642 12557364 Headache
125573642 12557364 Ocular hyperaemia
125573642 12557364 Product use issue
125573642 12557364 Visual acuity reduced

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
125573642 12557364 1 2008 2012 0
125573642 12557364 2 2012 0
125573642 12557364 3 2010 0
125573642 12557364 4 2006 201604 0
125573642 12557364 5 2012 0
125573642 12557364 6 2011 0