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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126031961 | 12603196 | 1 | I | 20160715 | 20160728 | 20160728 | EXP | PL-ELI_LILLY_AND_COMPANY-PL201607011632 | ELI LILLY AND CO | 56.00 | YR | M | Y | 0.00000 | 20160727 | CN | GB | PL |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126031961 | 12603196 | 1 | PS | GEMCITABINE HYDROCHLORIDE. | GEMCITABINE HYDROCHLORIDE | 1 | Intravenous (not otherwise specified) | 1800 MG, CYCLICAL (DAYS 1, 8, AND 15 EVERY 4 WEEKS) | U | 20509 | 1800 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126031961 | 12603196 | 1 | Ductal adenocarcinoma of pancreas |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126031961 | 12603196 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126031961 | 12603196 | Abdominal pain | |
| 126031961 | 12603196 | Anaemia | |
| 126031961 | 12603196 | Cardiotoxicity | |
| 126031961 | 12603196 | Diarrhoea | |
| 126031961 | 12603196 | Leukopenia | |
| 126031961 | 12603196 | Nausea | |
| 126031961 | 12603196 | Pain | |
| 126031961 | 12603196 | Thrombocytopenia | |
| 126031961 | 12603196 | Vomiting | |
| 126031961 | 12603196 | Weight increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |