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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
93954963 | 9395496 | 3 | F | 20160908 | 20130711 | 20160915 | EXP | CN-ASTELLAS-2013US007111 | ASTELLAS | WU S, LUO H, WANG L, ZHANG X, XIA B, XIE C, ET AL.. PHASE III RANDOMIZED STUDY OF ELECTIVE NODAL IRRADIATION PLUS ERLOTINIB COMBINED WITH CHEMOTHERAPY FOR ESOPHAGEAL SQUAMOUS CELL CARCINOMA [ABSTRACT NUMBER 4048].. JOURNAL OF CLINICAL ONCOLOGY. 2016;34 (SUPL 15):NO INFORMATION | 47.00 | YR | M | Y | 0.00000 | 20160915 | CN | GB | CN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
93954963 | 9395496 | 1 | PS | Erlotinib | ERLOTINIB | 1 | Oral | 21743 | 150 | MG | TABLET | QD | |||||||
93954963 | 9395496 | 2 | SS | CISPLATIN. | CISPLATIN | 1 | Intravenous (not otherwise specified) | 20 MG/M2, DAY 1-3 EVERY 4 WEEKS FOR 2 CYCLES | 0 | 20 | MG/M**2 | FORMULATION UNKNOWN | |||||||
93954963 | 9395496 | 3 | SS | PACLITAXEL. | PACLITAXEL | 1 | Intravenous (not otherwise specified) | 135 MG/M2, DAY 1 EVERY 4 WEEKS FOR TWO CYCLES | 0 | 135 | MG/M**2 | FORMULATION UNKNOWN |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
93954963 | 9395496 | 1 | Oesophageal squamous cell carcinoma |
93954963 | 9395496 | 2 | Oesophageal squamous cell carcinoma |
93954963 | 9395496 | 3 | Oesophageal squamous cell carcinoma |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
93954963 | 9395496 | DE |
93954963 | 9395496 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
93954963 | 9395496 | Gastrointestinal toxicity | |
93954963 | 9395496 | Haematotoxicity |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |