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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7915349 | 8245436 | I | 7915349-5 | 20111108 | 20111115 | EXP | PHHY2011RU099379 | NOVARTIS PHARMACEUTICAL CORPORATION | YR | F | Y | 20111115 | MD | RUSSIAN FEDERATION |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7915349 | 1018051656 | PS | ZOLEDRONOC ACID | 1 | INTRAVENOUS | UNK | 021817 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7915349 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7915349 | MYOSITIS |
| 7915349 | OEDEMA PERIPHERAL |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |