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
125927203 12592720 3 F 20160824 20160726 20160906 PER US-PFIZER INC-2016348916 PFIZER 52.00 YR F Y 0.00000 20160906 PH 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
125927203 12592720 1 PS GEMZAR GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 1185 MG, CYCLIC (3 WEEKS ON 1 OFF, X 6WEEKS - 1 CYCLE = 28 DAYS) GL216?3A 0 1185 MG
125927203 12592720 2 SS GEMZAR GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 1185 MG, CYCLIC (3 WEEKS ON 1 OFF, X 6WEEKS- 1 CYCLE = 28 DAYS) GL116?1B 0 1185 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125927203 12592720 1 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
125927203 12592720 OT
125927203 12592720 DE
125927203 12592720 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125927203 12592720 Death
125927203 12592720 Hepatic encephalopathy
125927203 12592720 Hepatic failure
125927203 12592720 Hyperbilirubinaemia
125927203 12592720 Jaundice hepatocellular

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
125927203 12592720 1 20160412 0
125927203 12592720 2 20160412 20160707 0