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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6523909 | 7235220 | I | 6523909-1 | 20090101 | 20091222 | 20091231 | EXP | US-ABBOTT-09P-163-0616232-00 | ABBOTT LABORATORIES | 65 | F | Y | 83.99 | KG | 20091231 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6523909 | 1012888016 | PS | HUMIRA | 1 | UNKNOWN | ||||||
6523909 | 1012888017 | SS | HUMIRA | 1 | UNKNOWN |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6523909 | 1012888016 | RHEUMATOID ARTHRITIS |
Outcome of event
Event ID | OUTC COD |
---|---|
6523909 | OT |
Reactions reported
Event ID | PT |
---|---|
6523909 | ABDOMINAL HERNIA |
6523909 | IMPAIRED HEALING |
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 |
---|---|---|---|---|---|
6523909 | 1012888016 | 20090618 | 20091001 |