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
125927193 12592719 3 F 20160621 20160824 20160726 20160901 PER US-PFIZER INC-2016348898 PFIZER 57.00 YR M Y 0.00000 20160901 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
125927193 12592719 1 PS GEMZAR GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 1500 MG, UNK (EVERY TWO WEEKS) GL21517B 0 1500 MG
125927193 12592719 2 SS GEMZAR GEMCITABINE HYDROCHLORIDE 1 UNK GL11601B 0
125927193 12592719 3 C CARBOPLATIN. CARBOPLATIN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125927193 12592719 1 Breast cancer
125927193 12592719 3 Breast cancer metastatic

Outcome of event

Event ID CASEID OUTC COD
125927193 12592719 DE
125927193 12592719 HO
125927193 12592719 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125927193 12592719 Coagulopathy
125927193 12592719 Encephalopathy
125927193 12592719 Hepatic failure
125927193 12592719 Renal failure

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
125927193 12592719 1 20151012 20160602 0
125927193 12592719 3 20151012 0