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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5745589 | 6705360 | I | 5745589-5 | 20080125 | 20080519 | PER | TPA2008A00121 | TAKEDA PHARMACEUTICALS NORTH AMERICA. | F | N | 20080501 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5745589 | 1009937390 | PS | ROZEREM | 1 | ORAL | 8 MG, PER ORAL | N | D | 21782 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5745589 | 1009937390 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 5745589 | TINNITUS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5745589 | CR |
| 5745589 | HP |
Therapies reported
| no results found |