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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8248770 | 7587656 | F | 8248770-9 | 20120326 | 20120331 | EXP | PHHY2010US59152 | NOVARTIS PHARMACEUTICAL CORPORATION | YR | F | Y | 20120330 | MD | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8248770 | 1019282823 | C | CALCIUM CARBONATE | 1 | |||||||
| 8248770 | 1019282822 | PS | RECLAST | 1 | INTRAVENOUS | UNK UKN, UNK | 021817 | ||||
| 8248770 | 1019282824 | C | VITAMIN D | 1 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8248770 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 8248770 | WRIST FRACTURE |
| 8248770 | GASTROINTESTINAL DISORDER |
| 8248770 | FALL |
| 8248770 | HOT FLUSH |
| 8248770 | FLATULENCE |
| 8248770 | ARTHRALGIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |