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
123558944 12355894 4 F 20160317 20160726 20160511 20160802 EXP DE-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-28794DE BOEHRINGER INGELHEIM 57.62 YR F Y 102.00000 KG 20160802 MD COUNTRY NOT SPECIFIED DE

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
123558944 12355894 1 PS VARGATEF NINTEDANIB 1 Oral 400 MG 205832 200 MG CAPSULE, SOFT BID
123558944 12355894 2 SS DOCETAXEL. DOCETAXEL 1 Intravenous (not otherwise specified) FORMULATION: LIQUID; DAILY DOSE: 75 MG/M2 BODY SURFACE AREA 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123558944 12355894 1 Lung adenocarcinoma
123558944 12355894 2 Lung adenocarcinoma

Outcome of event

Event ID CASEID OUTC COD
123558944 12355894 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123558944 12355894 Aspartate aminotransferase abnormal
123558944 12355894 Blood alkaline phosphatase increased
123558944 12355894 Blood bilirubin increased
123558944 12355894 Gamma-glutamyltransferase increased
123558944 12355894 Liver disorder
123558944 12355894 Muscular weakness
123558944 12355894 Nausea
123558944 12355894 Pharyngitis
123558944 12355894 White blood cell count 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
123558944 12355894 1 20160311 20160414 0
123558944 12355894 2 20160310 0