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
126339851 12633985 1 I 20160801 0 20160808 20160808 DIR 58.00 YR M N 82.50000 KG 20160805 N 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
126339851 12633985 1 PS CISPLATIN. CISPLATIN 1 D D 0
126339851 12633985 2 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 0 2000 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126339851 12633985 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126339851 12633985 Abdominal pain
126339851 12633985 Biliary tract infection
126339851 12633985 Blood culture positive
126339851 12633985 Device occlusion
126339851 12633985 Escherichia test positive
126339851 12633985 Fatigue
126339851 12633985 Hepatic enzyme increased
126339851 12633985 Nausea
126339851 12633985 Post procedural complication
126339851 12633985 Pyrexia
126339851 12633985 Vomiting

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
126339851 12633985 1 20160628 0
126339851 12633985 2 20160719 0