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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125317711 | 12531771 | 1 | I | 20160520 | 20160629 | 20160706 | 20160706 | EXP | FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-054066 | BRISTOL MYERS SQUIBB | 85.96 | YR | M | Y | 0.00000 | 20160706 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125317711 | 12531771 | 1 | PS | COUMADINE | WARFARIN SODIUM | 1 | Oral | UNK, QD | Y | 9218 | TABLET | QD | |||||||
125317711 | 12531771 | 2 | SS | KARDEGIC | ASPIRIN LYSINE | 1 | Oral | 75 MG, QD | Y | 0 | 75 | MG | QD | ||||||
125317711 | 12531771 | 3 | C | INEXIUM /01479302/ | ESOMEPRAZOLE MAGNESIUM | 1 | Unknown | U | 0 | ||||||||||
125317711 | 12531771 | 4 | C | INEXIUM /01479302/ | ESOMEPRAZOLE MAGNESIUM | 1 | Unknown | U | 0 | ||||||||||
125317711 | 12531771 | 5 | C | UROREC | SILODOSIN | 1 | Unknown | U | 0 | ||||||||||
125317711 | 12531771 | 6 | C | AVODART | DUTASTERIDE | 1 | Unknown | U | 0 | ||||||||||
125317711 | 12531771 | 7 | C | SEROPLEX | ESCITALOPRAM OXALATE | 1 | Unknown | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125317711 | 12531771 | 1 | Product used for unknown indication |
125317711 | 12531771 | 2 | Product used for unknown indication |
125317711 | 12531771 | 3 | Product used for unknown indication |
125317711 | 12531771 | 4 | Product used for unknown indication |
125317711 | 12531771 | 5 | Product used for unknown indication |
125317711 | 12531771 | 6 | Product used for unknown indication |
125317711 | 12531771 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125317711 | 12531771 | HO |
125317711 | 12531771 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125317711 | 12531771 | Anaemia | |
125317711 | 12531771 | Fall | |
125317711 | 12531771 | International normalised ratio increased | |
125317711 | 12531771 | Subdural haematoma |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |