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
119804379 11980437 9 F 20160618 20160901 20160129 20160913 EXP US-PFIZER INC-2016027709 PFIZER 70.00 YR M Y 96.15000 KG 20160913 CN 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
119804379 11980437 1 PS SUTENT SUNITINIB MALATE 1 50 MG, CYCLIC (28 DAYS ON/14 DAYS OFF) Y 421BA 21938 50 MG CAPSULE, HARD
119804379 11980437 2 C AMBIEN ZOLPIDEM TARTRATE 1 UNK 0
119804379 11980437 3 C PROTONIX PANTOPRAZOLE SODIUM 1 UNK 0
119804379 11980437 4 C HYDROCODONE BITARTRATE AND ACETAMINOPHEN ACETAMINOPHENHYDROCODONE BITARTRATE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119804379 11980437 1 Gastrointestinal stromal tumour

Outcome of event

Event ID CASEID OUTC COD
119804379 11980437 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
119804379 11980437 Abdominal pain
119804379 11980437 Back pain
119804379 11980437 Diarrhoea
119804379 11980437 Disease progression
119804379 11980437 Gastrointestinal stromal tumour
119804379 11980437 Haematoma
119804379 11980437 Pain
119804379 11980437 Weight 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
119804379 11980437 1 20160107 20160512 0