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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126953241 | 12695324 | 1 | I | 20160722 | 20160816 | 20160829 | 20160829 | EXP | FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-068323 | BRISTOL MYERS SQUIBB | 86.33 | YR | F | Y | 0.00000 | 20160829 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126953241 | 12695324 | 1 | PS | COUMADINE | WARFARIN SODIUM | 1 | Oral | 4 MG, UNK | Y | 9218 | 4 | MG | TABLET | ||||||
| 126953241 | 12695324 | 2 | C | CARDENSIEL | BISOPROLOL FUMARATE | 1 | Unknown | U | 0 | ||||||||||
| 126953241 | 12695324 | 3 | C | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | 40 MG, QD | U | 0 | 40 | MG | QD | ||||||
| 126953241 | 12695324 | 4 | C | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | 20 MG, QD | U | 0 | 20 | MG | QD | ||||||
| 126953241 | 12695324 | 5 | C | RAMIPRIL. | RAMIPRIL | 1 | Unknown | U | 0 | ||||||||||
| 126953241 | 12695324 | 6 | C | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Unknown | U | 0 | ||||||||||
| 126953241 | 12695324 | 7 | C | LEVOTHYROX | LEVOTHYROXINE | 1 | Unknown | U | 0 | ||||||||||
| 126953241 | 12695324 | 8 | C | SERESTA | OXAZEPAM | 1 | Unknown | U | 0 | ||||||||||
| 126953241 | 12695324 | 9 | C | DEXERYL /01579901/ | GLYCERINMINERAL OILPARAFFIN | 1 | Unknown | U | 0 | ||||||||||
| 126953241 | 12695324 | 10 | C | DOLIPRANE | ACETAMINOPHEN | 1 | Unknown | U | 0 | ||||||||||
| 126953241 | 12695324 | 11 | C | TRAMADOL. | TRAMADOL | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126953241 | 12695324 | 1 | Atrial fibrillation |
| 126953241 | 12695324 | 2 | Product used for unknown indication |
| 126953241 | 12695324 | 3 | Product used for unknown indication |
| 126953241 | 12695324 | 5 | Product used for unknown indication |
| 126953241 | 12695324 | 6 | Product used for unknown indication |
| 126953241 | 12695324 | 7 | Product used for unknown indication |
| 126953241 | 12695324 | 8 | Product used for unknown indication |
| 126953241 | 12695324 | 9 | Product used for unknown indication |
| 126953241 | 12695324 | 10 | Product used for unknown indication |
| 126953241 | 12695324 | 11 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126953241 | 12695324 | HO |
| 126953241 | 12695324 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126953241 | 12695324 | Fall | |
| 126953241 | 12695324 | Haemarthrosis | |
| 126953241 | 12695324 | Overdose |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |