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
127296341 12729634 1 I 20160830 20160909 20160909 EXP DE-TEVA-689427GER TEVA 0.00 M Y 103.00000 KG 20160909 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
127296341 12729634 1 PS PRAVASTATIN. PRAVASTATIN 1 Oral 1 DOSAGE FORMS DAILY; Y 76056 1 DF QD
127296341 12729634 2 SS SIMVASTATIN. SIMVASTATIN 1 Oral Y 76052
127296341 12729634 3 SS atorvastatin ATORVASTATIN 1 Oral 1 DOSAGE FORMS DAILY; Y 78773 1 DF QD
127296341 12729634 4 SS fenofibrat FENOFIBRATE 1 Oral 1 DOSAGE FORMS DAILY; Y 75753 1 DF QD
127296341 12729634 5 C OMEGA-3 ACIDS OMEGA-3 FATTY ACIDS 1 1500 MILLIGRAM DAILY; 0 1000 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127296341 12729634 1 Hypercholesterolaemia
127296341 12729634 2 Hypercholesterolaemia
127296341 12729634 3 Hypercholesterolaemia
127296341 12729634 4 Hypercholesterolaemia

Outcome of event

Event ID CASEID OUTC COD
127296341 12729634 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127296341 12729634 Arthralgia
127296341 12729634 Gout
127296341 12729634 Petechiae
127296341 12729634 Skin exfoliation
127296341 12729634 Tendon injury

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
127296341 12729634 1 20160223 20160406 0
127296341 12729634 3 20160218 20160223 0
127296341 12729634 4 20160614 20160810 0
127296341 12729634 5 20150921 20160614 0