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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4869118 | 5934364 | I | 4869118-3 | 20051219 | 20051221 | 20051230 | EXP | US-JNJFOC-20051105949 | CENTOCOR, INC. | 9 | YR | F | Y | 20051230 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4869118 | 1006774480 | SS | REMICADE | 1 | INTRAVENOUS | ||||||
| 4869118 | 1006774481 | SS | REMICADE | 1 | INTRAVENOUS | WEEK 6 | |||||
| 4869118 | 1006774482 | SS | REMICADE | 1 | INTRAVENOUS | WEEK 2 | |||||
| 4869118 | 1006774483 | SS | REMICADE | 1 | INTRAVENOUS | WEEK 0 | |||||
| 4869118 | 1006774484 | PS | REMICADE | 1 | INTRAVENOUS | ||||||
| 4869118 | 1006774485 | C | 6-MP | 2 | |||||||
| 4869118 | 1006774486 | C | ASACOL | 1 | |||||||
| 4869118 | 1006774487 | C | PREDNISONE 50MG TAB | 1 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4869118 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4869118 | INFUSION RELATED REACTION |
| 4869118 | NEPHROBLASTOMA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4869118 | 1006774480 | 1 | YR | ||
| 4869118 | 1006774481 | 1 | YR | ||
| 4869118 | 1006774482 | 1 | YR | ||
| 4869118 | 1006774483 | 1 | YR | ||
| 4869118 | 1006774484 | 1 | YR |