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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125415342 | 12541534 | 2 | F | 20160314 | 20160708 | 20160712 | PER | US-TEVA-575680USA | TEVA | 0.00 | M | Y | 95.34000 | KG | 20160712 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125415342 | 12541534 | 1 | PS | PROVIGIL | MODAFINIL | 1 | Unknown | 20717 | |||||||||||
125415342 | 12541534 | 2 | SS | PROVIGIL | MODAFINIL | 1 | 20717 | ||||||||||||
125415342 | 12541534 | 3 | C | HYDROCODONE | HYDROCODONE | 1 | 0 | ||||||||||||
125415342 | 12541534 | 4 | C | LEXAPRO | ESCITALOPRAM OXALATE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125415342 | 12541534 | 1 | Narcolepsy |
125415342 | 12541534 | 2 | Asthenia |
125415342 | 12541534 | 3 | Pain |
125415342 | 12541534 | 4 | Depression |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125415342 | 12541534 | Adverse event | |
125415342 | 12541534 | Product substitution issue | |
125415342 | 12541534 | Therapeutic response unexpected |
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 |
---|---|---|---|---|---|---|
125415342 | 12541534 | 1 | 1996 | 0 |