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
126128251 12612825 1 I 20100916 20110916 20160801 20160801 EXP US-ROCHE-803681 ROCHE 73.96 YR F Y 53.30000 KG 20160802 MD US US

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
126128251 12612825 1 PS Vismodegib VISMODEGIB 1 Oral 203388 900 MG CAPSULE QD
126128251 12612825 2 SS ETOPOSIDE. ETOPOSIDE 1 Intravenous (not otherwise specified) DOSE:100 MG/M2/DAY IV OVER 2 HRS ON DAYS 1-3 0 100 MG/M**2
126128251 12612825 3 SS CISPLATIN. CISPLATIN 1 Intravenous (not otherwise specified) DOSE: 75 MG/M2 IV OVER 2 HRS ON DAY 1 0 75 MG/M**2

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126128251 12612825 1 Small cell lung cancer
126128251 12612825 2 Small cell lung cancer
126128251 12612825 3 Small cell lung cancer

Outcome of event

Event ID CASEID OUTC COD
126128251 12612825 OT
126128251 12612825 HO
126128251 12612825 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126128251 12612825 Abdominal pain
126128251 12612825 Constipation
126128251 12612825 Lipase increased
126128251 12612825 Nausea
126128251 12612825 Neutrophil count decreased
126128251 12612825 Pain
126128251 12612825 Vomiting
126128251 12612825 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
126128251 12612825 1 20100909 20100914 0
126128251 12612825 2 20100909 20100915 0
126128251 12612825 3 20110909 20110915 0