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
126086972 12608697 2 F 20160721 20160801 20160729 20160805 EXP JP-ABBVIE-16P-087-1688640-00 ABBVIE 84.00 YR M Y 0.00000 20160805 MD JP JP

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
126086972 12608697 1 PS TRICOR FENOFIBRATE 1 Oral UNKNOWN 21656 160 MG QD
126086972 12608697 2 SS LIPIDIL FENOFIBRATE 1 Oral UNKNOWN 19304
126086972 12608697 3 SS LIPIDIL FENOFIBRATE 1 Oral UNKNOWN 19304
126086972 12608697 4 C ATORVASTATIN CALCIUM TRIHYDRATE ATORVASTATIN CALCIUM 1 Oral 0 10 MG QD
126086972 12608697 5 C AMLODIPINE BESILATE AMLODIPINE BESYLATE 1 Oral 0 5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126086972 12608697 1 Hyperlipidaemia
126086972 12608697 2 Lipids abnormal
126086972 12608697 3 Hyperlipidaemia
126086972 12608697 4 Hypercholesterolaemia
126086972 12608697 5 Hypertension

Outcome of event

Event ID CASEID OUTC COD
126086972 12608697 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126086972 12608697 Liver function test abnormal

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
126086972 12608697 1 20160623 20160721 0
126086972 12608697 2 201605 20160623 0