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
126302621 12630262 1 I 20160422 20160726 20160808 20160808 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-061940 BRISTOL MYERS SQUIBB 64.76 YR F Y 0.00000 20160808 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
126302621 12630262 1 PS COUMADINE WARFARIN SODIUM 1 Oral 8 MG, QD U 9218 8 MG TABLET QD
126302621 12630262 2 C NEO MERCAZOLE CARBIMAZOLE 1 Unknown 5 MG, QD U 0 5 MG QD
126302621 12630262 3 C UVEDOSE CHOLECALCIFEROL 1 Unknown U 0
126302621 12630262 4 C FLUIDABAK POVIDONE 1 Unknown U 0
126302621 12630262 5 C VITAMIN A /00056001/ RETINOL 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126302621 12630262 1 Pulmonary embolism
126302621 12630262 2 Product used for unknown indication
126302621 12630262 3 Product used for unknown indication
126302621 12630262 4 Product used for unknown indication
126302621 12630262 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126302621 12630262 HO
126302621 12630262 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126302621 12630262 Fall
126302621 12630262 Subdural haematoma
126302621 12630262 Subdural haematoma evacuation

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
126302621 12630262 1 20160109 0