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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4752388 | 5869456 | I | 4752388-X | 20050818 | 20050823 | EXP | 200510407BYL | BAYER PHARMACEUTICALS CORPORATION | N | 20050822 | JAPAN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4752388 | 1006354806 | PS | CIPROFLOXACIN HCL | 1 | D | D | 19847 | ||||
| 4752388 | 1006370578 | C | HYPNOTICS | 2 | |||||||
| 4752388 | 1006370583 | C | SEDATIVES | 2 | |||||||
| 4752388 | 1006370586 | C | ANTIANXIETICS | 2 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4752388 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4752388 | LOSS OF CONSCIOUSNESS |
| 4752388 | SOMNOLENCE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4752388 | FGN |
| 4752388 | HP |
| 4752388 | OTH |
Therapies reported
| no results found |