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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4785120 | 5889256 | I | 4785120-4 | 20041219 | 20050922 | 20050930 | EXP | DE-ABBOTT-05P-062-0312017-00 | ABBOTT | 57 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4785120 | 1006472968 | PS | HUMIRA | 1 | SUBCUTANEOUS | UNKNOWN | |||||
| 4785120 | 1006472969 | SS | HUMIRA | 1 | UNKNOWN | ||||||
| 4785120 | 1006472970 | SS | HUMIRA | 1 | UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4785120 | 1006472968 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4785120 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4785120 | BILE DUCT STONE |
| 4785120 | CHOLELITHIASIS |
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 |
|---|---|---|---|---|---|
| 4785120 | 1006472968 | 20040801 |