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
126429531 12642953 1 I 20160727 20160811 20160811 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-063535 BRISTOL MYERS SQUIBB 57.00 YR F Y 0.00000 20160811 OT 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
126429531 12642953 1 PS WARFARIN SODIUM. WARFARIN SODIUM 1 Unknown 5 MG, QD 9218 5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126429531 12642953 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126429531 12642953 HO
126429531 12642953 LT
126429531 12642953 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126429531 12642953 Acute kidney injury
126429531 12642953 Acute respiratory failure
126429531 12642953 Adrenal haemorrhage
126429531 12642953 Anticoagulation drug level below therapeutic
126429531 12642953 Pneumonia
126429531 12642953 Sepsis

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

no results found

Therapies reported

no results found