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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4784339 | 5888837 | I | 4784339-6 | 20050922 | 20050930 | EXP | PHBS2005NZ13971 | NOVARTIS PHARMACEUTICALS CORP. | 73 | YR | M | Y | 20050929 | MD | NEW ZEALAND |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4784339 | 1006470476 | PS | ZASTEN | 2 | ORAL | 1 MG/DAY | 21066 | ||||
| 4784339 | 1006470477 | C | ALLOPURINOL | 1 | ORAL | ||||||
| 4784339 | 1006470478 | C | PREDNISONE | 1 | ORAL | ||||||
| 4784339 | 1006470479 | C | DICLOFENAC | 2 | ORAL |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4784339 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4784339 | JAUNDICE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |