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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118676383 | 11867638 | 3 | F | 20150924 | 20160715 | 20151224 | 20160725 | EXP | IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-086316 | BRISTOL MYERS SQUIBB | 77.87 | YR | M | Y | 0.00000 | 20160725 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118676383 | 11867638 | 1 | PS | COUMADIN | WARFARIN SODIUM | 1 | Unknown | 2.5 MG, QD | 2472 | MG | Y | 9218 | 2.5 | MG | TABLET | QD | |||
| 118676383 | 11867638 | 2 | C | GLUCOPHAGE | METFORMIN HYDROCHLORIDE | 1 | Oral | 250 MG, UNK | U | 0 | 250 | MG | TABLET | ||||||
| 118676383 | 11867638 | 3 | C | PRADIF | TAMSULOSIN HYDROCHLORIDE | 1 | Oral | 0.4 MG, UNK | U | 0 | .4 | MG | CAPSULE | ||||||
| 118676383 | 11867638 | 4 | C | SIRDALUD | TIZANIDINE | 1 | Oral | U | 0 | TABLET | |||||||||
| 118676383 | 11867638 | 5 | C | FENTALGON | 2 | Unknown | U | 0 | |||||||||||
| 118676383 | 11867638 | 6 | C | DEPALGOS | ACETAMINOPHENOXYCODONE HYDROCHLORIDE | 1 | Oral | 1 UNIT, UNK | U | 0 | 1 | DF | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 118676383 | 11867638 | 1 | Product used for unknown indication |
| 118676383 | 11867638 | 2 | Product used for unknown indication |
| 118676383 | 11867638 | 3 | Product used for unknown indication |
| 118676383 | 11867638 | 4 | Product used for unknown indication |
| 118676383 | 11867638 | 5 | Product used for unknown indication |
| 118676383 | 11867638 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 118676383 | 11867638 | HO |
| 118676383 | 11867638 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 118676383 | 11867638 | Asthenia | |
| 118676383 | 11867638 | Cerebral haemorrhage | |
| 118676383 | 11867638 | Eyelid ptosis | |
| 118676383 | 11867638 | Gravitational oedema | |
| 118676383 | 11867638 | Hypophonesis | |
| 118676383 | 11867638 | Somnolence | |
| 118676383 | 11867638 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 118676383 | 11867638 | 1 | 20130109 | 20150924 | 0 |