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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126105061 | 12610506 | 1 | I | 201607 | 20160725 | 20160801 | 20160801 | PER | US-ELI_LILLY_AND_COMPANY-US201607011203 | ELI LILLY AND CO | 50.74 | YR | M | Y | 0.00000 | 20160801 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126105061 | 12610506 | 1 | PS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Unknown | 60 MG, UNKNOWN | U | 21427 | 60 | MG | CAPSULE | ||||||
| 126105061 | 12610506 | 2 | SS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Unknown | 30 MG, UNKNOWN | U | 21427 | 30 | MG | CAPSULE | ||||||
| 126105061 | 12610506 | 3 | SS | DULOXETINE HYDROCHLORIDE. | DULOXETINE HYDROCHLORIDE | 1 | Unknown | 60 MG, UNKNOWN | U | 0 | 60 | MG | |||||||
| 126105061 | 12610506 | 4 | SS | DULOXETINE HYDROCHLORIDE. | DULOXETINE HYDROCHLORIDE | 1 | Unknown | 30 MG, UNKNOWN | U | 0 | 30 | MG | |||||||
| 126105061 | 12610506 | 5 | C | VITAMIN D3 | CHOLECALCIFEROL | 1 | Unknown | UNK, UNKNOWN | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126105061 | 12610506 | 1 | Adjustment disorder with depressed mood |
| 126105061 | 12610506 | 3 | Adjustment disorder with depressed mood |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126105061 | 12610506 | Dizziness | |
| 126105061 | 12610506 | Feeling abnormal | |
| 126105061 | 12610506 | Hyperhidrosis | |
| 126105061 | 12610506 | Irritability | |
| 126105061 | 12610506 | Tension | |
| 126105061 | 12610506 | Withdrawal syndrome |
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 |
|---|---|---|---|---|---|---|
| 126105061 | 12610506 | 2 | 201605 | 201607 | 0 |