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
127295551 12729555 1 I 20160617 0 20160907 20160907 DIR FDA-CTU 56.00 YR M N 116.80000 KG 20160805 N PH US US

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
127295551 12729555 1 PS WARFARIN WARFARIN 1 Oral Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127295551 12729555 1 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
127295551 12729555 RI

Reactions reported

Event ID CASEID DRUG REC ACT PT
127295551 12729555 Abdominal discomfort
127295551 12729555 Dizziness
127295551 12729555 Faeces discoloured
127295551 12729555 Gastric haemorrhage
127295551 12729555 Haemorrhoids
127295551 12729555 Large intestine polyp

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

Event ID CASEID RPSR COD
127295551 12729555 HP

Therapies reported

no results found