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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126866762 | 12686676 | 2 | F | 20160714 | 20160914 | 20160825 | 20160923 | EXP | JP-ELI_LILLY_AND_COMPANY-JP201608011351 | ELI LILLY AND CO | 66.13 | YR | F | Y | 50.00000 | KG | 20160923 | CN | JP | JP |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126866762 | 12686676 | 1 | PS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Oral | 40 MG, EACH MORNING | Y | 21427 | 40 | MG | CAPSULE | QD | |||||
| 126866762 | 12686676 | 2 | SS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Y | 21427 | CAPSULE | ||||||||||
| 126866762 | 12686676 | 3 | C | NEUROTROPIN /06251301/ | ORYCTOLAGUS CUNICULUS SKIN | 1 | Oral | 2 DF, BID | 0 | 2 | DF | TABLET | BID | ||||||
| 126866762 | 12686676 | 4 | C | NEUROTROPIN /06251301/ | ORYCTOLAGUS CUNICULUS SKIN | 1 | 0 | TABLET | |||||||||||
| 126866762 | 12686676 | 5 | C | MOHRUS | KETOPROFEN | 1 | Transdermal | 1 DF, QD | 0 | 1 | DF | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126866762 | 12686676 | 1 | Pain in extremity |
| 126866762 | 12686676 | 2 | Neuralgia |
| 126866762 | 12686676 | 3 | Pain in extremity |
| 126866762 | 12686676 | 4 | Neuralgia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126866762 | 12686676 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126866762 | 12686676 | Abdominal discomfort | |
| 126866762 | 12686676 | Cold sweat | |
| 126866762 | 12686676 | Diarrhoea | |
| 126866762 | 12686676 | Dizziness | |
| 126866762 | 12686676 | Enteritis | |
| 126866762 | 12686676 | Nausea | |
| 126866762 | 12686676 | Off label use | |
| 126866762 | 12686676 | Vomiting | |
| 126866762 | 12686676 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 126866762 | 12686676 | 1 | 20160714 | 20160714 | 0 | |
| 126866762 | 12686676 | 3 | 20160518 | 0 | ||
| 126866762 | 12686676 | 5 | 20160627 | 0 |