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
126488971 12648897 1 I 201201 20160728 20160812 20160812 EXP US-VALIDUS PHARMACEUTICALS LLC-US-2016VAL002370 VALIDUS 0.00 Y 0.00000 20160812 MD 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
126488971 12648897 1 PS LASIX FUROSEMIDE 1 UNK Y 16273
126488971 12648897 2 SS PLAVIX CLOPIDOGREL BISULFATE 1 UNK U 0
126488971 12648897 3 SS TORSEMIDE. TORSEMIDE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126488971 12648897 1 Product used for unknown indication
126488971 12648897 2 Product used for unknown indication
126488971 12648897 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126488971 12648897 OT
126488971 12648897 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126488971 12648897 Amino acid level abnormal
126488971 12648897 Cardiac failure congestive
126488971 12648897 Fluid retention
126488971 12648897 High density lipoprotein increased
126488971 12648897 Joint swelling
126488971 12648897 Pain in extremity
126488971 12648897 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
126488971 12648897 1 2011 0
126488971 12648897 2 2011 0
126488971 12648897 3 2011 0