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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4542789 | 5706634 | F | 4542789-7 | 20041210 | 20041210 | 20041231 | EXP | PHHO2004FI17572 | NOVARTIS PHARMACEUTICALS CORP. | 71 | YR | F | Y | 60 | KG | 20041231 | OT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4542789 | 1005547053 | PS | ZOLEDRONIC ACID VS PLACEBO | 2 | INTRAVENOUS | DOUBLE-BLIND | |||||
| 4542789 | 1005547054 | C | KALCIPOS-D | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4542789 | 1005547053 | OSTEOPOROTIC FRACTURE |
| 4542789 | 1005547054 | OSTEOPOROTIC FRACTURE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4542789 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4542789 | HEADACHE |
| 4542789 | NAUSEA |
| 4542789 | PYREXIA |
| 4542789 | SYNCOPE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4542789 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4542789 | 1005547053 | 20041209 |