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
125391321 12539132 1 I 20160617 0 20160707 20160707 DIR 65.05 YR M N 78.90000 KG 20160630 N MD 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
125391321 12539132 1 PS CISPLATIN. CISPLATIN 1 0 143 MG
125391321 12539132 2 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 0 4020 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125391321 12539132 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125391321 12539132 Abdominal pain
125391321 12539132 Anaemia
125391321 12539132 Asthenia
125391321 12539132 Blood magnesium decreased
125391321 12539132 Blood potassium decreased
125391321 12539132 Dehydration
125391321 12539132 Platelet count decreased
125391321 12539132 Urinary tract infection
125391321 12539132 White blood cell count decreased

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
125391321 12539132 1 20160613 0
125391321 12539132 2 20160613 0