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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4785121 | 5889257 | I | 4785121-6 | 20041126 | 20050922 | 20050930 | EXP | DE-ABBOTT-05P-062-0312026-00 | ABBOTT | 68 | YR | F | Y | 20050930 | GERMANY |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4785121 | 1006472972 | PS | HUMIRA | 1 | UNKNOWN | ||||||
4785121 | 1006472973 | SS | HUMIRA | 1 | UNKNOWN | ||||||
4785121 | 1006472974 | C | METHOTREXATE SODIUM | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4785121 | 1006472972 | DRUG USE FOR UNKNOWN INDICATION |
4785121 | 1006472974 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
4785121 | HO |
Reactions reported
Event ID | PT |
---|---|
4785121 | FALL |
4785121 | GRAND MAL CONVULSION |
4785121 | HYPOKINESIA |
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 |
---|---|---|---|---|---|
4785121 | 1006472972 | 20040401 | 20041001 | 8 | MON |
4785121 | 1006472973 | 20031201 | 20040201 | 8 | MON |
4785121 | 1006472974 | 20031201 | 20040201 | 2 | MON |