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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127456761 | 12745676 | 1 | I | 20160909 | 20160915 | 20160915 | EXP | US-SUNOVION-2016SUN002236 | SUNOVION | 0.00 | F | Y | 0.00000 | 20160915 | CN | US | US |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127456761 | 12745676 | 1 | PS | LUNESTA | ESZOPICLONE | 1 | Oral | 3 MG, UNK | U | 21476 | 3 | MG | TABLET | ||||||
127456761 | 12745676 | 2 | SS | LUNESTA | ESZOPICLONE | 1 | Oral | 6 MG, SINGLE | U | 21476 | 6 | MG | TABLET | QD |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127456761 | 12745676 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127456761 | 12745676 | Abdominal discomfort | |
127456761 | 12745676 | Anxiety | |
127456761 | 12745676 | Crying | |
127456761 | 12745676 | Extra dose administered | |
127456761 | 12745676 | Insomnia | |
127456761 | 12745676 | Intentional overdose | |
127456761 | 12745676 | Presyncope | |
127456761 | 12745676 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |