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
116202163 11620216 3 F 2010 20160906 20151012 20160913 EXP DE-ASTELLAS-2015US036665 ASTELLAS 63.00 YR M Y 0.00000 20160913 MD DE DE

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
116202163 11620216 1 PS AMBISOME AMPHOTERICIN B 1 Intravenous (not otherwise specified) 50740 250 MG INJECTION
116202163 11620216 2 SS FUNGIZONE AMPHOTERICIN B 1 Unknown U 0 250 MG FORMULATION UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116202163 11620216 1 Product used for unknown indication
116202163 11620216 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
116202163 11620216 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
116202163 11620216 Blood creatinine increased
116202163 11620216 Drug dispensing error
116202163 11620216 Product name confusion
116202163 11620216 Wrong drug administered

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
116202163 11620216 1 2010 0
116202163 11620216 2 2010 0