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
126290221 12629022 1 I 20160726 20160808 20160808 EXP IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-061881 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160808 CN IT IT

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
126290221 12629022 1 PS COUMADIN WARFARIN SODIUM 1 Oral UNK U 9218 TABLET
126290221 12629022 2 C ATIMOS FORMOTEROL 1 Unknown U 0
126290221 12629022 3 C VYTORIN EZETIMIBESIMVASTATIN 1 Unknown U 0
126290221 12629022 4 C LANOXIN DIGOXIN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126290221 12629022 1 Anticoagulant therapy
126290221 12629022 2 Product used for unknown indication
126290221 12629022 3 Product used for unknown indication
126290221 12629022 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126290221 12629022 DE
126290221 12629022 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126290221 12629022 Cerebral haemorrhage
126290221 12629022 Contusion
126290221 12629022 Laceration

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
126290221 12629022 1 20150101 20151216 0