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
126092351 12609235 1 I 20101026 20110311 20160801 20160801 EXP US-ROCHE-772026 ROCHE 81.23 YR F Y 80.00000 KG 20160801 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
126092351 12609235 1 PS Vismodegib VISMODEGIB 1 Oral 26/OCT/2010: LAST ADMINISTERED DATE OF VISMODEGIB. U 203388
126092351 12609235 2 SS CISPLATIN. CISPLATIN 1 Intravenous (not otherwise specified) U 0 75 MG/M**2
126092351 12609235 3 SS ETOPOSIDE. ETOPOSIDE 1 Intravenous (not otherwise specified) U 0 100 MG/M**2

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126092351 12609235 1 Small cell lung cancer extensive stage
126092351 12609235 2 Small cell lung cancer extensive stage
126092351 12609235 3 Small cell lung cancer extensive stage

Outcome of event

Event ID CASEID OUTC COD
126092351 12609235 DE
126092351 12609235 OT
126092351 12609235 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126092351 12609235 Blood creatinine increased
126092351 12609235 Diarrhoea
126092351 12609235 Fatigue
126092351 12609235 Febrile neutropenia
126092351 12609235 Platelet count decreased
126092351 12609235 Sepsis
126092351 12609235 Urinary tract infection

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
126092351 12609235 1 20101019 20101026 0
126092351 12609235 2 20101019 0
126092351 12609235 3 20101019 0