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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4964434 | 6026858 | I | 4964434-9 | 20060322 | 20060331 | EXP | 2006-03-1549 | SCHERING-PLOUGH CORPORATION | 67 | YR | F | N | 20060326 | OT | JAPAN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4964434 | 1007135815 | PS | CELESTAMINE TAB | 1 | ORAL | 1 TAB ORAL | U | U | 14215 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4964434 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4964434 | AGRANULOCYTOSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4964434 | FGN |
| 4964434 | HP |
| 4964434 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4964434 | 1007135815 | 20030701 | 20030701 |