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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4250482 | 3944978 | F | 1 | 4250482-3 | 20031125 | 20031210 | EXP | NSADSS2003019873 | CENTOCOR, INC. | UNK | N | 20031209 | MD |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4250482 | 1004434717 | PS | REMICADE | 1 | INTRAVENOUS DRIP | 5 MG/KG, INTRAVENOUS DRIP | U | U |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4250482 | 1004434717 | CROHN'S DISEASE |
Outcome of event
Event ID | OUTC COD |
---|---|
4250482 | OT |
Reactions reported
Event ID | PT |
---|---|
4250482 | ANTINUCLEAR ANTIBODY POSITIVE |
4250482 | LUPUS-LIKE SYNDROME |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
4250482 | HP |
4250482 | LIT |
Therapies reported
no results found |