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
125742461 12574246 1 I 20160621 20160711 20160720 20160720 EXP DE-TEVA-676027GER TEVA 72.00 YR F Y 61.00000 KG 20160720 MD DE DE

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
125742461 12574246 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral 80 MILLIGRAM DAILY; U 76052 80 MG QD
125742461 12574246 2 SS adenuric FEBUXOSTAT 1 80 MILLIGRAM DAILY; U 0 80 MG QD
125742461 12574246 3 C valsacor 320/25 mg 2 Oral 1 DOSAGE FORMS DAILY; 0 1 DF QD
125742461 12574246 4 C RANEXA RANOLAZINE 1 Oral 750 DOSAGE FORMS DAILY; 0 375 DF BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125742461 12574246 1 Hyperlipidaemia
125742461 12574246 2 Hyperuricaemia
125742461 12574246 3 Hypertension
125742461 12574246 4 Arrhythmia

Outcome of event

Event ID CASEID OUTC COD
125742461 12574246 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125742461 12574246 Hypoaesthesia
125742461 12574246 Myopathy
125742461 12574246 Renal failure

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found