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
127264331 12726433 1 I 20151107 20160825 20160908 20160908 EXP PA20150795 FR-VALIDUS PHARMACEUTICALS LLC-FR-2016VAL002576 VALIDUS 83.00 YR M Y 0.00000 20160908 OT FR FR

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
127264331 12726433 1 PS FUROSEMIDE. FUROSEMIDE 1 Oral UNK, TID Y 16273
127264331 12726433 2 SS COLCHIMAX /01722001/ COLCHICINEOPIUMTIEMONIUM METHYLSULFATE 1 Oral UNK, TID Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127264331 12726433 1 Cardiac failure
127264331 12726433 2 Gout

Outcome of event

Event ID CASEID OUTC COD
127264331 12726433 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127264331 12726433 Acute kidney injury
127264331 12726433 Dehydration
127264331 12726433 Diarrhoea
127264331 12726433 Hypokalaemia
127264331 12726433 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
127264331 12726433 1 20151030 20151107 0
127264331 12726433 2 20151030 20151107 0