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
125227951 12522795 1 I 20120312 20160616 20160701 20160701 EXP BR20160396 FR-VALIDUS PHARMACEUTICALS LLC-FR-2016VAL002198 VALIDUS 77.00 YR F Y 0.00000 20160701 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
125227951 12522795 1 PS FUROSEMIDE. FUROSEMIDE 1 Oral 20 MG, DAILY Y 16273 20 MG
125227951 12522795 2 SS COTAREG HYDROCHLOROTHIAZIDEVALSARTAN 1 Oral 1 DF, DAILY Y 0 1 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125227951 12522795 1 Product used for unknown indication
125227951 12522795 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125227951 12522795 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125227951 12522795 Acute kidney injury
125227951 12522795 Atrioventricular block complete
125227951 12522795 Hyperkalaemia

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
125227951 12522795 1 20120312 0
125227951 12522795 2 20120312 0