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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123860923 | 12386092 | 3 | F | 20160503 | 20160923 | 20160519 | 20160930 | EXP | IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-035709 | BRISTOL MYERS SQUIBB | 82.68 | YR | F | Y | 0.00000 | 20160930 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123860923 | 12386092 | 1 | PS | COUMADIN | WARFARIN SODIUM | 1 | Oral | 3.75 MG, QD | Y | 9218 | 3.75 | MG | TABLET | QD | |||||
| 123860923 | 12386092 | 2 | C | VERAPAMIL | VERAPAMIL HYDROCHLORIDE | 1 | Unknown | U | 0 | ||||||||||
| 123860923 | 12386092 | 3 | C | PAROXETIN /00830801/ | PAROXETINE HYDROCHLORIDE | 1 | Oral | 20 MG, UNK | U | 0 | 20 | MG | TABLET | ||||||
| 123860923 | 12386092 | 4 | C | LANSOPRAZOLE. | LANSOPRAZOLE | 1 | Oral | 30 MG, UNK | U | 0 | 30 | MG | TABLET | ||||||
| 123860923 | 12386092 | 5 | C | TARGIN | NALOXONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDE | 1 | Unknown | U | 0 | ||||||||||
| 123860923 | 12386092 | 6 | C | DIBASE | CHOLECALCIFEROL | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123860923 | 12386092 | 1 | Atrial fibrillation |
| 123860923 | 12386092 | 2 | Product used for unknown indication |
| 123860923 | 12386092 | 3 | Product used for unknown indication |
| 123860923 | 12386092 | 4 | Product used for unknown indication |
| 123860923 | 12386092 | 5 | Product used for unknown indication |
| 123860923 | 12386092 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123860923 | 12386092 | OT |
| 123860923 | 12386092 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123860923 | 12386092 | Drug abuse | |
| 123860923 | 12386092 | International normalised ratio increased | |
| 123860923 | 12386092 | Overdose | |
| 123860923 | 12386092 | Toxicity to various agents |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |