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
127240941 12724094 1 I 2011 20160728 20160908 20160908 EXP US-SA-2016SA150399 AVENTIS 63.00 YR A M Y 0.00000 20160908 CN 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
127240941 12724094 1 SS LASIX FUROSEMIDE 1 Unknown Y UNKNOWN 0
127240941 12724094 2 PS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown U UNKNOWN 20839
127240941 12724094 3 SS TORSEMIDE. TORSEMIDE 1 Unknown U UNKNOWN 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127240941 12724094 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127240941 12724094 Amino acid level abnormal
127240941 12724094 Cardiac failure congestive
127240941 12724094 Fluid retention
127240941 12724094 High density lipoprotein increased
127240941 12724094 Weight 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
127240941 12724094 1 2011 0
127240941 12724094 2 2011 0
127240941 12724094 3 2011 0