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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127091251 | 12709125 | 1 | I | 20160520 | 0 | 20160901 | 20160901 | DIR | 49.00 | YR | F | N | 130.00000 | LBS | 20160831 | N | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127091251 | 12709125 | 1 | PS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Oral | Y | N | C340850A | 0 | 270 | DF | CAPSULE | TID | ||||
127091251 | 12709125 | 3 | C | LAMICAL XR | 2 | 0 | |||||||||||||
127091251 | 12709125 | 5 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127091251 | 12709125 | 1 | Depression |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127091251 | 12709125 | Amnesia | |
127091251 | 12709125 | Confusional state | |
127091251 | 12709125 | Feeling abnormal |
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 |
---|---|---|---|---|---|---|
127091251 | 12709125 | 1 | 20160509 | 20160621 | 0 |