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
125242761 12524276 1 I 20150713 20160704 20160704 PER DE-LUPIN PHARMACEUTICALS INC.-E2B_00003937 LUPIN 0.00 F Y 66.00000 KG 20160704 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
125242761 12524276 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral Y Y UNKNOWN 78103 20 MG QD
125242761 12524276 2 SS Atorvastatin ATORVASTATIN 1 Oral Y Y UNKNOWN 0 10 MG QD
125242761 12524276 3 SS FLUVASTATIN FLUVASTATIN SODIUM 1 Oral Y Y UNKNOWN 0 20 MG QD
125242761 12524276 4 SS ROSUVASTATIN. ROSUVASTATIN 1 Oral Y Y UNKNOWN 0 10 MG QD
125242761 12524276 5 SS BEZAFIBRAT BEZAFIBRATE 1 Oral Y Y UNKNOWN 0 400 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125242761 12524276 1 Hyperlipidaemia
125242761 12524276 2 Hyperlipidaemia
125242761 12524276 3 Hyperlipidaemia
125242761 12524276 4 Hyperlipidaemia
125242761 12524276 5 Hyperlipidaemia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125242761 12524276 Decreased appetite
125242761 12524276 Dizziness Dizziness
125242761 12524276 Nausea

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
125242761 12524276 1 20121002 20121127 0
125242761 12524276 2 20121128 20130124 0
125242761 12524276 3 20130125 20130611 0
125242761 12524276 4 20140218 20140407 0
125242761 12524276 5 20150513 20150623 0