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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 106785733 | 10678573 | 3 | F | 20120904 | 20160804 | 20141229 | 20160816 | EXP | CA-ELI_LILLY_AND_COMPANY-CA201412007367 | ELI LILLY AND CO | 0.00 | M | Y | 0.00000 | 20160816 | CN | CA | CA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 106785733 | 10678573 | 1 | PS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Oral | 60 MG, EACH MORNING | U | U | 21427 | 60 | MG | CAPSULE | QD | ||||
| 106785733 | 10678573 | 2 | SS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Unknown | UNK, UNKNOWN | U | U | 21427 | CAPSULE | |||||||
| 106785733 | 10678573 | 3 | SS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Unknown | 60 MG, EACH MORNING | U | U | 21427 | 60 | MG | CAPSULE | QD | ||||
| 106785733 | 10678573 | 4 | SS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Unknown | 2 DF, EACH EVENING | U | U | 21427 | 2 | DF | CAPSULE | QD | ||||
| 106785733 | 10678573 | 5 | SS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Unknown | 6-8 CAPSULES | U | U | 21427 | CAPSULE | |||||||
| 106785733 | 10678573 | 6 | C | ALTACE | RAMIPRIL | 1 | Unknown | UNK, UNKNOWN | U | U | 0 | ||||||||
| 106785733 | 10678573 | 7 | C | ASPIRIN /00002701/ | ASPIRIN | 1 | Unknown | UNK, UNKNOWN | U | U | 0 | ||||||||
| 106785733 | 10678573 | 8 | C | PROSCAR | FINASTERIDE | 1 | Unknown | UNK, UNKNOWN | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 106785733 | 10678573 | 1 | Major depression |
| 106785733 | 10678573 | 6 | Blood pressure measurement |
| 106785733 | 10678573 | 7 | Product used for unknown indication |
| 106785733 | 10678573 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 106785733 | 10678573 | OT |
| 106785733 | 10678573 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 106785733 | 10678573 | Amnesia | |
| 106785733 | 10678573 | Anger | |
| 106785733 | 10678573 | Anxiety | |
| 106785733 | 10678573 | Chest pain | |
| 106785733 | 10678573 | Depressed mood | |
| 106785733 | 10678573 | Energy increased | |
| 106785733 | 10678573 | Homicide | |
| 106785733 | 10678573 | Impulsive behaviour | |
| 106785733 | 10678573 | Judgement impaired | |
| 106785733 | 10678573 | Loss of consciousness | |
| 106785733 | 10678573 | Mania | |
| 106785733 | 10678573 | Overdose | |
| 106785733 | 10678573 | Personality change | |
| 106785733 | 10678573 | Physical assault |
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 |
|---|---|---|---|---|---|---|
| 106785733 | 10678573 | 1 | 2009 | 0 | ||
| 106785733 | 10678573 | 2 | 201204 | 0 | ||
| 106785733 | 10678573 | 3 | 20120904 | 0 | ||
| 106785733 | 10678573 | 4 | 20120904 | 0 | ||
| 106785733 | 10678573 | 5 | 20120904 | 0 |