The Safety Rates Drug Report

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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
93913993 9391399 3 F 20160908 20130709 20160915 EXP CN-ASTELLAS-2013US006995 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 [ABS 4048].. JOURNAL OF CLINICAL ONCOLOGY. 2016;34(SUPP 15):NO INFORMATION 66.00 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
93913993 9391399 1 PS Erlotinib ERLOTINIB 1 Oral U 21743 150 MG TABLET QD
93913993 9391399 2 SS CISPLATIN. CISPLATIN 1 Intravenous (not otherwise specified) 20 MG/M2, DAY 1-3, EVERY 4 WEEKS FOR 2 CYCLES U 0 20 MG/M**2 FORMULATION UNKNOWN
93913993 9391399 3 SS PACLITAXEL. PACLITAXEL 1 Intravenous (not otherwise specified) 135 MG/M2, DAY 1 EVERY 4 WEEKS FOR 2 CYCLES U 0 135 MG/M**2 FORMULATION UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
93913993 9391399 1 Oesophageal squamous cell carcinoma
93913993 9391399 2 Oesophageal squamous cell carcinoma
93913993 9391399 3 Oesophageal squamous cell carcinoma

Outcome of event

Event ID CASEID OUTC COD
93913993 9391399 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
93913993 9391399 Gastrointestinal toxicity
93913993 9391399 Haematotoxicity

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found