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
126838831 12683883 1 I 20160817 20160825 20160825 EXP BR-PFIZER INC-2016392380 PFIZER 71.00 YR F Y 0.00000 20160825 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
126838831 12683883 1 PS XALATAN LATANOPROST 1 Ophthalmic 1 DROP ON BOTH EYES, UNK L26349 20597 EYE DROPS, SOLUTION
126838831 12683883 2 C OCUPRESS /01264102/ 2 Ophthalmic 1 DROP IN BOTH EYES, UNK 0 2 GTT

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126838831 12683883 1 Intraocular pressure increased
126838831 12683883 2 Intraocular pressure increased

Outcome of event

Event ID CASEID OUTC COD
126838831 12683883 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126838831 12683883 Cataract
126838831 12683883 Drug intolerance
126838831 12683883 Eye irritation
126838831 12683883 Foreign body sensation in eyes
126838831 12683883 Head discomfort
126838831 12683883 Intraocular pressure increased
126838831 12683883 Ocular discomfort
126838831 12683883 Vision blurred
126838831 12683883 Visual impairment

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
126838831 12683883 1 20160814 0
126838831 12683883 2 20160702 0