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
126098321 12609832 1 I 20160621 20160718 20160801 20160801 EXP DE-LUPIN PHARMACEUTICALS INC.-E2B_00005883 LUPIN 72.00 YR F Y 61.00000 KG 20160801 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
126098321 12609832 1 SS Adenuric FEBUXOSTAT 1 Unknown UNKNOWN 0 80 MG QD
126098321 12609832 2 PS SIMVASTATIN. SIMVASTATIN 1 Oral UNKNOWN 78103 80 MG QD
126098321 12609832 3 C Valsacor 320/25 mg 2 Oral 0 1 DF QD
126098321 12609832 4 C RANEXA RANOLAZINE 1 Oral 0 375 DF BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126098321 12609832 1 Hyperuricaemia
126098321 12609832 2 Hyperlipidaemia
126098321 12609832 3 Hypertension
126098321 12609832 4 Arrhythmia

Outcome of event

Event ID CASEID OUTC COD
126098321 12609832 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126098321 12609832 Hypoaesthesia
126098321 12609832 Myopathy
126098321 12609832 Renal failure

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

no results found

Therapies reported

no results found