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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5060440 | 6111687 | I | 5060440-7 | 20060322 | 20060630 | PER | A03200601654 | SANOFI-SYNTHELABO, INC. | F | N | 20060622 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5060440 | 1007502667 | PS | AMBIEN | 1 | ORAL | 12.5 MG QD ORAL | D | D | 21774 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
5060440 | OT |
Reactions reported
Event ID | PT |
---|---|
5060440 | DRUG INEFFECTIVE |
5060440 | FALL |
5060440 | LOSS OF CONSCIOUSNESS |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
5060440 | CSM |
Therapies reported
no results found |