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
126737791 12673779 1 I 201605 20160808 20160822 20160822 EXP ES-AGEMED-215927334 ES-VALIDUS PHARMACEUTICALS LLC-ES-2016VAL002471 VALIDUS 86.00 YR F Y 0.00000 20160822 MD ES ES

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
126737791 12673779 1 PS FUROSEMIDE. FUROSEMIDE 1 Oral UNK U 16273 TABLET
126737791 12673779 2 SS RENITEC /00574902/ ENALAPRIL MALEATE 1 Oral 5 MG, QD Y 0 5 MG TABLET
126737791 12673779 3 SS ADIRO ASPIRIN 1 Oral 100 MG, QD 0 100 MG GASTRO-RESISTANT TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126737791 12673779 1 Chronic kidney disease
126737791 12673779 2 Hypertension
126737791 12673779 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126737791 12673779 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126737791 12673779 Acute kidney injury
126737791 12673779 Drug interaction
126737791 12673779 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
126737791 12673779 1 201605 0
126737791 12673779 2 2016 20160520 0
126737791 12673779 3 2016 0