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
126215421 12621542 1 I 20100713 20110311 20160804 20160804 EXP US-ROCHE-766291 ROCHE 47.00 YR M Y 93.30000 KG 20160804 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
126215421 12621542 1 PS Vismodegib VISMODEGIB 1 Oral 150 MG, QD, MOST RECENT DOSE: 13/JUL/2010 Y NOT REPORTED 203388 150 MG CAPSULE QD
126215421 12621542 2 SS Erlotinib ERLOTINIB 1 Oral 75 MG, QD, MOST RECENT DOSE: 13/JUL/2010 Y NOT REPORTED 53728 75 MG TABLET QD
126215421 12621542 3 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 750 MG/M2, UNK, MOST RECENT DOSE: 13/JUL/2010 Y 0 750 MG/M**2

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126215421 12621542 1 Neoplasm
126215421 12621542 2 Neoplasm
126215421 12621542 3 Neoplasm

Outcome of event

Event ID CASEID OUTC COD
126215421 12621542 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126215421 12621542 Neutrophil count decreased
126215421 12621542 Platelet count decreased
126215421 12621542 Pruritus
126215421 12621542 White blood cell count decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found