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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124185312 | 12418531 | 2 | F | 201602 | 20160704 | 20160531 | 20160711 | EXP | DE-AMGEN-DEUSP2016067807 | AMGEN | 76.00 | YR | E | F | Y | 0.00000 | 20160711 | MD | DE | DE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124185312 | 12418531 | 1 | PS | PROLIA | DENOSUMAB | 1 | Subcutaneous | 60 MG, UNK | U | 125320 | 60 | MG | SOLUTION FOR INJECTION | ||||||
| 124185312 | 12418531 | 2 | C | CALCIUM | CALCIUM | 1 | 0 | ||||||||||||
| 124185312 | 12418531 | 3 | C | VITAMIN D | CHOLECALCIFEROL | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124185312 | 12418531 | 1 | Osteoporosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124185312 | 12418531 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124185312 | 12418531 | Burning sensation | |
| 124185312 | 12418531 | Myalgia | |
| 124185312 | 12418531 | Paraesthesia | |
| 124185312 | 12418531 | Paralysis |
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 |
|---|---|---|---|---|---|---|
| 124185312 | 12418531 | 1 | 20160217 | 0 |