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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4817167 | 6040616 | I | 4817167-3 | 20050606 | 20051018 | PER | PHEH2005US06359 | NOVARTIS PHARMACEUTICALS CORP. | F | N | 20050829 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4817167 | 1006582324 | PS | ZOMETA | 1 | INTRAVENOUS | 4 MG, INTRAVENOUS | U | U | 21223 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4817167 | 1006582324 | MULTIPLE MYELOMA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4817167 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4817167 | BLOOD ALBUMIN DECREASED |
| 4817167 | BLOOD CALCIUM DECREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4817167 | CR |
| 4817167 | HP |
Therapies reported
| no results found |