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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6816342 | 7887185 | I | 6816342-6 | 20100621 | 20100705 | EXP | PHHY2010PK40952 | NOVARTIS PHARMACEUTICAL CORPORATION | 70 | YR | F | Y | 20100705 | MD | PAKISTAN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6816342 | 1014031733 | PS | ZOLEDRONIC | 1 | INTRAVENOUS | 5 MG/100 ML | 21817 | ||||
| 6816342 | 1014031734 | SS | ZOLEDRONIC | 1 | 021817 | ||||||
| 6816342 | 1014031735 | C | CALCIUM WITH VITAMIN D | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6816342 | 1014031733 | FEMUR FRACTURE |
| 6816342 | 1014031734 | SURGERY |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6816342 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6816342 | PAIN |
| 6816342 | PAIN IN EXTREMITY |
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 |
|---|---|---|---|---|---|
| 6816342 | 1014031733 | 20100615 |