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
126817971 12681797 1 I 20160413 20160810 20160824 20160824 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-066759 BRISTOL MYERS SQUIBB 88.08 YR M Y 0.00000 20160824 CN FR FR

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
126817971 12681797 1 PS COUMADINE WARFARIN SODIUM 1 Oral 1 DF, QD Y 9218 1 DF TABLET QD
126817971 12681797 2 C NORSET MIRTAZAPINE 1 Unknown 15 MG, QD U 0 15 MG TABLET QD
126817971 12681797 3 C CASODEX BICALUTAMIDE 1 Unknown U 0
126817971 12681797 4 C SERESTA OXAZEPAM 1 Unknown U 0
126817971 12681797 5 C MOVICOL POLYETHYLENE GLYCOL 3350POTASSIUM CHLORIDESODIUM BICARBONATESODIUM CHLORIDE 1 Unknown U 0
126817971 12681797 6 C FOLIC ACID. FOLIC ACID 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126817971 12681797 1 Product used for unknown indication
126817971 12681797 2 Product used for unknown indication
126817971 12681797 3 Product used for unknown indication
126817971 12681797 4 Product used for unknown indication
126817971 12681797 5 Product used for unknown indication
126817971 12681797 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126817971 12681797 OT
126817971 12681797 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126817971 12681797 Fall
126817971 12681797 Product use issue
126817971 12681797 Subdural haematoma

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
126817971 12681797 1 20160413 0