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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127250261 | 12725026 | 1 | I | 20160819 | 20160826 | 20160908 | 20160908 | EXP | IN-ELI_LILLY_AND_COMPANY-IN201608013102 | ELI LILLY AND CO | 76.00 | YR | M | Y | 0.00000 | 20160901 | CN | IN | IN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127250261 | 12725026 | 1 | PS | PEMETREXED | PEMETREXED | 1 | Unknown | 1000 MG, CYCLICAL | 21462 | 1000 | MG | INJECTION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127250261 | 12725026 | 1 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127250261 | 12725026 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127250261 | 12725026 | Appetite disorder | |
| 127250261 | 12725026 | Asthenia | |
| 127250261 | 12725026 | Diarrhoea | |
| 127250261 | 12725026 | Feeling abnormal | |
| 127250261 | 12725026 | Haemoglobin decreased | |
| 127250261 | 12725026 | Platelet count decreased | |
| 127250261 | 12725026 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 127250261 | 12725026 | 1 | 20160428 | 0 |