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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127069821 | 12706982 | 1 | I | 20151005 | 20160901 | 20160901 | EXP | PHJP2015JP017517 | NOVARTIS | 69.00 | YR | F | Y | 0.00000 | 20160901 | OT | JP | JP |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127069821 | 12706982 | 1 | PS | ZOMETA | ZOLEDRONIC ACID | 1 | Intravenous drip | 4 MG, UNK | Y | 21223 | 4 | MG | SOLUTION FOR INJECTION | ||||||
| 127069821 | 12706982 | 2 | SS | DENOSUMAB | DENOSUMAB | 1 | Unknown | UNK | Y | 0 | |||||||||
| 127069821 | 12706982 | 3 | SS | DENOSUMAB | DENOSUMAB | 1 | Y | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127069821 | 12706982 | 1 | Metastases to bone |
| 127069821 | 12706982 | 2 | Breast cancer metastatic |
| 127069821 | 12706982 | 3 | Metastases to bone |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127069821 | 12706982 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127069821 | 12706982 | Bone loss | |
| 127069821 | 12706982 | Femur fracture | |
| 127069821 | 12706982 | Pain in extremity |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |