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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7789031 | 8163385 | I | 7789031-1 | 20110901 | 20110920 | 20110930 | EXP | JP-JNJFOC-20110909639 | CENTOCOR ORTHO BIOTECH INC. | 47 | YR | M | Y | 62 | KG | 20110930 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7789031 | 1017677100 | SS | REMICADE | 1 | INTRAVENOUS | SEVENTH DOSE | |||||
7789031 | 1017677101 | PS | REMICADE | 1 | INTRAVENOUS | FIRST DOSE |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7789031 | 1017677100 | COLITIS ULCERATIVE |
Outcome of event
Event ID | OUTC COD |
---|---|
7789031 | HO |
Reactions reported
Event ID | PT |
---|---|
7789031 | HAEMORRHAGE SUBCUTANEOUS |
7789031 | GENERALISED OEDEMA |
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 |
---|---|---|---|---|---|
7789031 | 1017677100 | 20110816 | |||
7789031 | 1017677101 | 20101122 |