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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127001121 | 12700112 | 1 | I | 20160817 | 20160830 | 20160830 | EXP | JP-ELI_LILLY_AND_COMPANY-JP201608013018 | ELI LILLY AND CO | 0.00 | A | Y | 0.00000 | 20160829 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127001121 | 12700112 | 1 | PS | ERBITUX | CETUXIMAB | 1 | Intravenous (not otherwise specified) | 400 MG/M2, WEEKLY (1/W) | U | U | 125084 | 400 | MG/M**2 | /wk | |||||
| 127001121 | 12700112 | 2 | SS | ERBITUX | CETUXIMAB | 1 | Intravenous (not otherwise specified) | 250 MG/M2, WEEKLY (1/W) | U | U | 125084 | 250 | MG/M**2 | /wk | |||||
| 127001121 | 12700112 | 3 | SS | CAPECITABINE. | CAPECITABINE | 1 | Oral | 1000 MG/M2, CYCLICAL | U | U | 0 | 1000 | MG/M**2 | ||||||
| 127001121 | 12700112 | 4 | SS | OXALIPLATIN. | OXALIPLATIN | 1 | Unknown | 85 MG/M2, OTHER | U | U | 0 | 85 | MG/M**2 | ||||||
| 127001121 | 12700112 | 5 | C | MINOCYCLINE | MINOCYCLINEMINOCYCLINE HYDROCHLORIDE | 1 | Oral | UNK UNK, PRN | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127001121 | 12700112 | 1 | Colorectal cancer metastatic |
| 127001121 | 12700112 | 3 | Colorectal cancer metastatic |
| 127001121 | 12700112 | 4 | Colorectal cancer metastatic |
| 127001121 | 12700112 | 5 | Premedication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127001121 | 12700112 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127001121 | 12700112 | Decreased appetite |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |