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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125853222 | 12585322 | 2 | F | 20160505 | 20160810 | 20160724 | 20160812 | EXP | US-AMGEN-USASL2016094310 | AMGEN | 78.00 | YR | E | F | Y | 63.49000 | KG | 20160812 | OT | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125853222 | 12585322 | 1 | PS | PROLIA | DENOSUMAB | 1 | Unknown | UNK | 125320 | SOLUTION FOR INJECTION | |||||||||
| 125853222 | 12585322 | 2 | SS | COUMADIN | WARFARIN SODIUM | 1 | Oral | 4 MG, QD (5 MG ON DAY 5) | 0 | 4 | MG | QD | |||||||
| 125853222 | 12585322 | 3 | C | DIGOXIN. | DIGOXIN | 1 | 125 MG, QD | 0 | 125 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125853222 | 12585322 | 1 | Osteoporosis |
| 125853222 | 12585322 | 2 | Atrial fibrillation |
| 125853222 | 12585322 | 3 | Atrial fibrillation |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125853222 | 12585322 | OT |
| 125853222 | 12585322 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125853222 | 12585322 | Cerebral haemorrhage |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |