Person who experienced the adverse event (patient)
Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125662201 | 12566220 | 1 | I | 20160707 | 20160718 | 20160718 | EXP | JP-SA-2016SA128595 | AVENTIS | 0.00 | A | Y | 0.00000 | 20160718 | PH | JP | JP |
Drug(s) used by person
Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125662201 | 12566220 | 1 | PS | MYSLEE | ZOLPIDEM TARTRATE | 1 | Oral | BEFORE BEDTIME | UNKNOWN | 19908 | TABLET | QD | |||||||
125662201 | 12566220 | 2 | C | SELENICA-R | VALPROATE SODIUM | 1 | Oral | AFTER BREAKFAST | 0 | 1000 | MG | QD |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125662201 | 12566220 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125662201 | 12566220 | Epilepsy | |
125662201 | 12566220 | Middle insomnia | |
125662201 | 12566220 | Somnolence |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |