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
127182351 12718235 1 I 20160705 20160829 20160906 20160906 EXP US-SA-2016SA162096 AVENTIS 71.00 YR E M Y 0.00000 20160906 OT US JP

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
127182351 12718235 1 PS OXALIPLATIN. OXALIPLATIN 1 Intravenous (not otherwise specified) UNKNOWN 21759 100 MG/M**2 /cycle
127182351 12718235 2 C AMLODIPINE AMLODIPINE BESYLATE 1 Unknown 0
127182351 12718235 3 C RANITIDINE. RANITIDINE 1 Unknown 0
127182351 12718235 4 C POLARAMINE DEXCHLORPHENIRAMINE MALEATE 1 Unknown 0 INJECTION
127182351 12718235 5 C PACLITAXEL. PACLITAXEL 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127182351 12718235 1 Adenocarcinoma gastric
127182351 12718235 2 Hypertension
127182351 12718235 3 Prophylaxis
127182351 12718235 4 Premedication

Outcome of event

Event ID CASEID OUTC COD
127182351 12718235 HO
127182351 12718235 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127182351 12718235 Acute respiratory distress syndrome
127182351 12718235 Disease progression
127182351 12718235 Drug ineffective
127182351 12718235 Enterocolitis
127182351 12718235 Febrile neutropenia
127182351 12718235 Pneumonia
127182351 12718235 Pneumonitis
127182351 12718235 Pyrexia

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
127182351 12718235 1 20160506 20160617 0
127182351 12718235 2 2011 0
127182351 12718235 3 20160722 0
127182351 12718235 4 20160722 20160722 0