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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7487528 | 7949696 | I | 7487528-5 | 20110301 | 20110510 | 20110518 | EXP | DK-AMGEN-DNKCT2011024237 | AMGENSAFETY | 79 | YR | F | Y | 20110518 | MD | DENMARK |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7487528 | 1016525680 | PS | DENOSUMAB | 2 | SUBCUTANEOUS | 1 ML, Q6MO |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7487528 | 1016525680 | OSTEOPOROSIS POSTMENOPAUSAL |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7487528 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 7487528 | DUODENAL ULCER |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 7487528 | 1016525680 | 20080410 |