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
127106641 12710664 1 I 20160822 20160902 20160902 EXP BR-PFIZER INC-2016399951 PFIZER 66.00 YR M Y 83.00000 KG 20160902 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
127106641 12710664 1 PS XALATAN LATANOPROST 1 Ophthalmic UNK U 20597 EYE DROPS, SOLUTION
127106641 12710664 2 C AZORGA BRINZOLAMIDETIMOLOL MALEATE 1 UNK 0
127106641 12710664 3 C GINKO BILOBA GINKGO 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127106641 12710664 1 Glaucoma

Outcome of event

Event ID CASEID OUTC COD
127106641 12710664 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127106641 12710664 Drug ineffective
127106641 12710664 Visual acuity reduced

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

no results found

Therapies reported

no results found