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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125903182 | 12590318 | 2 | F | 20141024 | 20160831 | 20160725 | 20160901 | EXP | US-ALLERGAN-1663626US | ALLERGAN | 31.00 | YR | M | Y | 86.20000 | KG | 20160901 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125903182 | 12590318 | 1 | PS | NORCO | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | U | U | 40148 | TABLET | |||||||||
125903182 | 12590318 | 2 | SS | LUNESTA | ESZOPICLONE | 1 | Oral | 3 MG, QHS | Y | Y | 0 | 3 | MG | QD | |||||
125903182 | 12590318 | 3 | SS | LYRICA | PREGABALIN | 1 | 300 MG, BID | Y | Y | 0 | 300 | MG | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125903182 | 12590318 | 1 | Back pain |
125903182 | 12590318 | 2 | Insomnia |
125903182 | 12590318 | 3 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125903182 | 12590318 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125903182 | 12590318 | Brain injury | |
125903182 | 12590318 | Cognitive disorder | |
125903182 | 12590318 | Sedation |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
125903182 | 12590318 | 2 | 20141024 | 0 |