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
118314252 11831425 2 F 20151125 20160714 20151214 20160725 EXP IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-083619 BRISTOL MYERS SQUIBB 92.10 YR F Y 0.00000 20160725 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
118314252 11831425 1 PS COUMADIN WARFARIN SODIUM 1 Oral 1 UNIT, UNK 9218 1 DF TABLET
118314252 11831425 2 C ATORVASTATIN ATORVASTATIN 1 Unknown U 0
118314252 11831425 3 C EUTIROX LEVOTHYROXINE SODIUM 1 Oral 50 ?G, UNK U 0 50 UG TABLET
118314252 11831425 4 C LASITONE FUROSEMIDESPIRONOLACTONE 1 Unknown 1 UNK, UNK U 0 1 DF CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118314252 11831425 1 Embolic stroke
118314252 11831425 2 Product used for unknown indication
118314252 11831425 3 Product used for unknown indication
118314252 11831425 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
118314252 11831425 HO
118314252 11831425 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118314252 11831425 Fall
118314252 11831425 Head injury
118314252 11831425 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
118314252 11831425 1 20150101 20151125 0