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
127219501 12721950 1 I 20160829 20160907 20160907 EXP US-ELI_LILLY_AND_COMPANY-US201608013187 ELI LILLY AND CO 0.00 M Y 0.00000 20160902 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
127219501 12721950 1 PS GEMZAR GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 1500 MG, CYCLICAL GL21517B 20509 1500 MG INJECTION
127219501 12721950 2 C CARBOPLATIN. CARBOPLATIN 1 UNK 0
127219501 12721950 3 C RIFAXIMIN RIFAXIMIN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127219501 12721950 1 Breast cancer
127219501 12721950 2 Breast cancer metastatic

Outcome of event

Event ID CASEID OUTC COD
127219501 12721950 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127219501 12721950 Coagulopathy
127219501 12721950 Encephalopathy
127219501 12721950 Hepatic failure
127219501 12721950 Hepatorenal syndrome
127219501 12721950 Renal failure
127219501 12721950 Toxicity to various agents

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
127219501 12721950 1 20151012 20160602 0
127219501 12721950 2 20151012 0