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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125658141 | 12565814 | 1 | I | 20160629 | 20160707 | 20160718 | 20160718 | EXP | TW-ELI_LILLY_AND_COMPANY-TW201607002230 | ELI LILLY AND CO | 74.00 | YR | M | Y | 0.00000 | 20160715 | CN | TW | TW |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125658141 | 12565814 | 1 | PS | ALIMTA | PEMETREXED DISODIUM | 1 | Unknown | UNK, UNKNOWN | U | 21462 | 700 | MG | INJECTION | ||||||
| 125658141 | 12565814 | 2 | C | STRESSTAB /02364401/ | 2 | Unknown | UNK, UNKNOWN | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125658141 | 12565814 | 1 | Lung neoplasm malignant |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125658141 | 12565814 | HO |
| 125658141 | 12565814 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125658141 | 12565814 | Death | |
| 125658141 | 12565814 | Oral mucosal eruption | |
| 125658141 | 12565814 | Platelet count decreased | |
| 125658141 | 12565814 | White blood cell count 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 |
|---|---|---|---|---|---|---|
| 125658141 | 12565814 | 1 | 20160622 | 0 |