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
122258932 12225893 2 F 20151001 20160707 20160331 20160720 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-021550 BRISTOL MYERS SQUIBB 77.00 YR F Y 0.00000 20160720 MD 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
122258932 12225893 1 PS COUMADIN WARFARIN SODIUM 1 Unknown UNK Y 9218
122258932 12225893 2 SS COUMADIN WARFARIN SODIUM 1 Y 9218

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122258932 12225893 1 Pulmonary embolism
122258932 12225893 2 Deep vein thrombosis

Outcome of event

Event ID CASEID OUTC COD
122258932 12225893 OT
122258932 12225893 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122258932 12225893 Acute kidney injury
122258932 12225893 Constipation
122258932 12225893 Gastrointestinal haemorrhage
122258932 12225893 Haemorrhagic anaemia
122258932 12225893 Hypokalaemia
122258932 12225893 Hypomagnesaemia
122258932 12225893 Internal haemorrhage
122258932 12225893 International normalised ratio increased
122258932 12225893 Pyelonephritis
122258932 12225893 Transfusion

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
122258932 12225893 1 201308 0