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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125658151 | 12565815 | 1 | I | 20160713 | 20160718 | 20160718 | PER | US-ELI_LILLY_AND_COMPANY-US201607004915 | ELI LILLY AND CO | 0.00 | F | Y | 0.00000 | 20160718 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125658151 | 12565815 | 1 | PS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Oral | 60 MG, QD | U | 21427 | 60 | MG | CAPSULE | QD | |||||
| 125658151 | 12565815 | 2 | SS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | U | 21427 | CAPSULE | ||||||||||
| 125658151 | 12565815 | 3 | SS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | U | 21427 | CAPSULE | ||||||||||
| 125658151 | 12565815 | 4 | SS | DULOXETINE HYDROCHLORIDE. | DULOXETINE HYDROCHLORIDE | 1 | Oral | UNK UNK, UNKNOWN | 0 | ||||||||||
| 125658151 | 12565815 | 5 | SS | DULOXETINE HYDROCHLORIDE. | DULOXETINE HYDROCHLORIDE | 1 | Oral | 10 MG, QD | 0 | 10 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125658151 | 12565815 | 1 | Fibromyalgia |
| 125658151 | 12565815 | 2 | Anxiety |
| 125658151 | 12565815 | 3 | Neuropathy peripheral |
| 125658151 | 12565815 | 4 | Neuropathy peripheral |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125658151 | 12565815 | Anxiety | |
| 125658151 | 12565815 | Depression | |
| 125658151 | 12565815 | Sleep disorder | |
| 125658151 | 12565815 | Wrong technique in product usage process |
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 |
|---|---|---|---|---|---|---|
| 125658151 | 12565815 | 1 | 2008 | 0 | ||
| 125658151 | 12565815 | 4 | 2014 | 0 |