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
125942012 12594201 2 F 201607 20160921 20160726 20160929 EXP BR-PFIZER INC-2016347829 PFIZER 0.00 F Y 0.00000 20160929 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
125942012 12594201 1 PS XALATAN LATANOPROST 1 Ophthalmic 1 DROP IN EACH EYE EVERY NIGHT U 8Q2392 20597 2 GTT EYE DROPS, SOLUTION QD
125942012 12594201 2 SS XALATAN LATANOPROST 1 UNK U M00717 20597 EYE DROPS, SOLUTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125942012 12594201 1 Glaucoma

Outcome of event

Event ID CASEID OUTC COD
125942012 12594201 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125942012 12594201 Accidental exposure to product
125942012 12594201 Deafness
125942012 12594201 Incorrect dose administered
125942012 12594201 Product dropper issue

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
125942012 12594201 1 20160713 0