The Safety Rates Drug Report

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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
125192931 12519293 1 I 20160307 20160701 20160701 PER DE-LUPIN PHARMACEUTICALS INC.-E2B_00005087 LUPIN 0.00 E F Y 70.00000 KG 20160624 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
125192931 12519293 1 PS SIMVASTATIN. SIMVASTATIN 1 Unknown Y UNKNOWN 78103 40 MG
125192931 12519293 2 SS SIMVASTATIN. SIMVASTATIN 1 Unknown DOSE REDUCED Y UNKNOWN 78103
125192931 12519293 3 SS Atorvastatin ATORVASTATIN 1 Unknown Y UNKNOWN 0 80 MG
125192931 12519293 4 SS Atorvastatin ATORVASTATIN 1 Unknown DOSE REDUCED Y UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125192931 12519293 1 Hypercholesterolaemia
125192931 12519293 3 Hypercholesterolaemia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125192931 12519293 Myalgia

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
125192931 12519293 1 2012 0
125192931 12519293 3 201502 0