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
126093431 12609343 1 I 20101006 20110311 20160801 20160801 EXP US-ROCHE-772056 ROCHE 58.43 YR F Y 70.00000 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
126093431 12609343 1 PS Vismodegib VISMODEGIB 1 Oral NOT REPORTED 203388 3150 MG QD
126093431 12609343 2 SS ETOPOSIDE. ETOPOSIDE 1 Intravenous (not otherwise specified) 100 MG/M2, QDX3D/21DC; ADMINISTERED OVER 2 HOURS ON DAYS 1-3 0 100 MG/M**2
126093431 12609343 3 SS CISPLATIN. CISPLATIN 1 Intravenous (not otherwise specified) 75 MG/M2, Q21D ; ADMINISTERED OVER 2 HOURS ON DAY 1 0 75 MG/M**2

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126093431 12609343 1 Small cell lung cancer
126093431 12609343 2 Small cell lung cancer
126093431 12609343 3 Small cell lung cancer

Outcome of event

Event ID CASEID OUTC COD
126093431 12609343 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126093431 12609343 Hyponatraemia
126093431 12609343 Neutrophil 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
126093431 12609343 1 20100728 20101103 0
126093431 12609343 2 20100728 20101103 0
126093431 12609343 3 20100728 20101103 0