The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
127450711 12745071 1 I 20160730 20160901 20160915 20160915 EXP PB20160968 FR-ACCORD-043935 ACCORD 71.00 YR F Y 0.00000 20160915 OT FR FR

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
127450711 12745071 1 PS CISPLATIN ACCORD CISPLATIN 1 Intravenous (not otherwise specified) U 206774
127450711 12745071 2 SS NAVELBINE VINORELBINE TARTRATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127450711 12745071 1 Lung carcinoma cell type unspecified stage II
127450711 12745071 2 Lung carcinoma cell type unspecified stage II

Outcome of event

Event ID CASEID OUTC COD
127450711 12745071 LT
127450711 12745071 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127450711 12745071 Arterial thrombosis
127450711 12745071 Decreased appetite
127450711 12745071 Diarrhoea
127450711 12745071 Intestinal infarction
127450711 12745071 Nausea
127450711 12745071 Neutropenia
127450711 12745071 Vomiting
127450711 12745071 Weight 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
127450711 12745071 1 20160719 20160720 0
127450711 12745071 2 20160719 20160730 0