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
98930962 9893096 2 F 20160722 20140213 20160722 EXP TR-BRISTOL-MYERS SQUIBB COMPANY-20169314 BRISTOL MYERS SQUIBB 63.00 YR F Y 0.00000 20160722 CN TR TR

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
98930962 9893096 1 PS WARFARIN SODIUM. WARFARIN SODIUM 1 Unknown 5 MG, QD Y 9218 5 MG QD
98930962 9893096 2 I HERBAL MIXTURE HERBALS 1 Unknown Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98930962 9893096 1 Pulmonary embolism
98930962 9893096 2 Arthralgia

Outcome of event

Event ID CASEID OUTC COD
98930962 9893096 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
98930962 9893096 Drug interaction
98930962 9893096 Haematuria
98930962 9893096 Rash

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

no results found

Therapies reported

no results found