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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125637541 | 12563754 | 1 | I | 20160124 | 20160701 | 20160716 | 20160716 | EXP | FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-055247 | BRISTOL MYERS SQUIBB | 86.36 | YR | M | Y | 0.00000 | 20160716 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125637541 | 12563754 | 1 | PS | COUMADINE | WARFARIN SODIUM | 1 | Oral | 2 MG, QD | U | 9218 | 2 | MG | TABLET | QD | |||||
125637541 | 12563754 | 2 | SS | COUMADINE | WARFARIN SODIUM | 1 | U | 9218 | TABLET | ||||||||||
125637541 | 12563754 | 3 | C | ZOXAN /00639302/ | DOXAZOSIN MESYLATE | 1 | Oral | 8 MG, QD | U | 0 | 8 | MG | QD | ||||||
125637541 | 12563754 | 4 | C | LASILIX /00032601/ | FUROSEMIDE | 1 | Oral | 60 MG, UNK | U | 0 | 60 | MG | |||||||
125637541 | 12563754 | 5 | C | MONOPROST | LATANOPROST | 1 | Unknown | 1 DF, QD | U | 0 | 1 | DF | EYE DROPS | QD | |||||
125637541 | 12563754 | 6 | C | TIAPRIDAL | TIAPRIDE HYDROCHLORIDE | 1 | Unknown | U | 0 | ||||||||||
125637541 | 12563754 | 7 | C | TRAMADOL. | TRAMADOL | 1 | Oral | U | 0 | ||||||||||
125637541 | 12563754 | 8 | C | TRUSOPT | DORZOLAMIDE HYDROCHLORIDE | 1 | Unknown | UNK, QD | U | 0 | EYE DROPS | QD | |||||||
125637541 | 12563754 | 9 | C | INEXIUM /01479302/ | ESOMEPRAZOLE MAGNESIUM | 1 | Oral | 20 MG, UNK | U | 0 | 20 | MG | |||||||
125637541 | 12563754 | 10 | C | AUGMENTIN | AMOXICILLINCLAVULANATE POTASSIUM | 1 | Oral | UNK | U | 0 | |||||||||
125637541 | 12563754 | 11 | C | SOLUPRED /00016201/ | PREDNISOLONE | 1 | Oral | 20 MG, QD | U | 0 | 20 | MG | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125637541 | 12563754 | 1 | Arrhythmia |
125637541 | 12563754 | 2 | Atrial fibrillation |
125637541 | 12563754 | 3 | Product used for unknown indication |
125637541 | 12563754 | 4 | Product used for unknown indication |
125637541 | 12563754 | 5 | Product used for unknown indication |
125637541 | 12563754 | 6 | Product used for unknown indication |
125637541 | 12563754 | 7 | Product used for unknown indication |
125637541 | 12563754 | 8 | Product used for unknown indication |
125637541 | 12563754 | 9 | Product used for unknown indication |
125637541 | 12563754 | 10 | Product used for unknown indication |
125637541 | 12563754 | 11 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125637541 | 12563754 | HO |
125637541 | 12563754 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125637541 | 12563754 | Anaemia | |
125637541 | 12563754 | Bronchitis | |
125637541 | 12563754 | Fall | |
125637541 | 12563754 | Haematoma | |
125637541 | 12563754 | International normalised ratio increased | |
125637541 | 12563754 | Lumbar vertebral fracture | |
125637541 | 12563754 | Osteoporosis | |
125637541 | 12563754 | Overdose | |
125637541 | 12563754 | Rib fracture |
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 |
---|---|---|---|---|---|---|
125637541 | 12563754 | 1 | 20160123 | 0 | ||
125637541 | 12563754 | 10 | 20160119 | 20160123 | 0 | |
125637541 | 12563754 | 11 | 20160119 | 0 |