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
127462962 12746296 2 F 20160422 20160920 20160915 20160926 EXP JP-ELI_LILLY_AND_COMPANY-JP201605002412 ELI LILLY AND CO 74.38 YR M Y 54.50000 KG 20160925 CN JP 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
127462962 12746296 1 PS CYRAMZA RAMUCIRUMAB 1 Intravenous (not otherwise specified) 400 MG, OTHER Y N 125477 400 MG INJECTION
127462962 12746296 2 SS PACLITAXEL. PACLITAXEL 1 Intravenous (not otherwise specified) 110 MG, OTHER Y 0 110 MG
127462962 12746296 3 SS FILGRASTIM FILGRASTIM 1 Subcutaneous 75 UG, UNK D 0 75 UG
127462962 12746296 4 SS MAXIPIME CEFEPIME HYDROCHLORIDE 1 Intravenous (not otherwise specified) 1 G, BID D 0 1 G BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127462962 12746296 1 Gastric cancer stage IV
127462962 12746296 2 Gastric cancer stage IV
127462962 12746296 3 Febrile neutropenia
127462962 12746296 4 Febrile neutropenia

Outcome of event

Event ID CASEID OUTC COD
127462962 12746296 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127462962 12746296 Febrile neutropenia
127462962 12746296 Interstitial lung disease
127462962 12746296 Pleural effusion

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
127462962 12746296 1 20160408 20160408 0
127462962 12746296 2 20160408 20160415 0
127462962 12746296 3 20160422 20160425 0
127462962 12746296 4 20160422 20160427 0