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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125871891 | 12587189 | 1 | I | 20160528 | 20160713 | 20160725 | 20160725 | EXP | FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-059097 | BRISTOL MYERS SQUIBB | 93.47 | YR | F | Y | 0.00000 | 20160725 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125871891 | 12587189 | 1 | PS | COUMADINE | WARFARIN SODIUM | 1 | Oral | 0.5 OTHER, UNK | Y | 9218 | .5 | DF | TABLET | ||||||
125871891 | 12587189 | 2 | SS | COUMADINE | WARFARIN SODIUM | 1 | Oral | 0.75 OTHER, UNK | Y | 9218 | .75 | DF | TABLET | ||||||
125871891 | 12587189 | 3 | C | NEBIVOLOL. | NEBIVOLOL | 1 | Oral | 0.5 DF, QD | U | 0 | .5 | DF | QD | ||||||
125871891 | 12587189 | 4 | C | LASILIX FAIBLE | FUROSEMIDE | 1 | Oral | 1 DF, QD | U | 0 | 1 | DF | TABLET | QD | |||||
125871891 | 12587189 | 5 | C | INEXIUM /01479302/ | ESOMEPRAZOLE MAGNESIUM | 1 | Oral | 1 DF, QD | U | 0 | 1 | DF | GASTRO-RESISTANT TABLET | QD | |||||
125871891 | 12587189 | 6 | C | SERESTA | OXAZEPAM | 1 | Oral | 1 DF, QD | U | 0 | 1 | DF | TABLET | QD | |||||
125871891 | 12587189 | 7 | C | ZYMAD | CHOLECALCIFEROL | 1 | Oral | 1 DF, QD | U | 0 | 1 | DF | ORAL SOLUTION | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125871891 | 12587189 | 1 | Product used for unknown indication |
125871891 | 12587189 | 3 | Hypertension |
125871891 | 12587189 | 4 | Product used for unknown indication |
125871891 | 12587189 | 5 | Gastrooesophageal reflux disease |
125871891 | 12587189 | 6 | Anxiety |
125871891 | 12587189 | 7 | Vitamin D deficiency |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125871891 | 12587189 | OT |
125871891 | 12587189 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125871891 | 12587189 | Fall | |
125871891 | 12587189 | 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 |
---|---|---|---|---|---|---|
125871891 | 12587189 | 1 | 20160614 | 0 | ||
125871891 | 12587189 | 7 | 20160509 | 0 |