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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122714553 | 12271455 | 3 | F | 20150905 | 20160725 | 20160415 | 20160801 | EXP | DE-AMGEN-DEUSP2016045184 | AMGEN | 56.00 | YR | A | F | Y | 80.00000 | KG | 20160801 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122714553 | 12271455 | 1 | PS | PROLIA | DENOSUMAB | 1 | Subcutaneous | 60 MG, Q6MO | 93.9840012 | MG | Y | 125320 | 60 | MG | SOLUTION FOR INJECTION | ||||
| 122714553 | 12271455 | 2 | C | DEKRISTOL | CHOLECALCIFEROL | 1 | Oral | 20000 UNK, QWK | 0 | /wk |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122714553 | 12271455 | 1 | Osteoporosis postmenopausal |
| 122714553 | 12271455 | 2 | Vitamin D deficiency |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122714553 | 12271455 | HO |
| 122714553 | 12271455 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122714553 | 12271455 | Drug ineffective | |
| 122714553 | 12271455 | Fall | |
| 122714553 | 12271455 | Femur fracture |
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 |
|---|---|---|---|---|---|---|
| 122714553 | 12271455 | 1 | 20141121 | 20151124 | 0 | |
| 122714553 | 12271455 | 2 | 2014 | 0 |