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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5154069 | 6170784 | I | 5154069-X | 20061021 | 20061114 | 20061120 | EXP | DE-RB-004363-06 | RECKITTBENCKISER | F | Y | 20061120 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5154069 | 1007866524 | PS | SUBUTEX | 1 | UNKNOWN |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5154069 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5154069 | DRUG WITHDRAWAL SYNDROME |
| 5154069 | FALL |
| 5154069 | FRACTURE |
| 5154069 | PAIN |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |