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
127295671 12729567 1 I 20160719 0 20160907 20160907 DIR FDA-CTU 67.00 YR M N 147.60000 KG 20160907 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
127295671 12729567 1 PS WARFARIN WARFARIN 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127295671 12729567 1 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
127295671 12729567 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127295671 12729567 Dizziness
127295671 12729567 Gastric haemorrhage
127295671 12729567 Palpitations
127295671 12729567 Radiation proctitis
127295671 12729567 Rectal haemorrhage

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

Event ID CASEID RPSR COD
127295671 12729567 HP

Therapies reported

no results found