Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8622207 | 8745685 | I | 8622207-X | 20120803 | 20120822 | 20120827 | EXP | CA-AMGEN-CANSP2012053268 | AMGENSAFETY | 81 | YR | F | Y | 50 | KG | 20120826 | CN | CANADA |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8622207 | 1020665166 | PS | PROLIA | 1 | SUBCUTANEOUS | 60 MG, Q6MO |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8622207 | 1020665166 | OSTEOPOROSIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8622207 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 8622207 | PELVIC FRACTURE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |