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
127133822 12713382 2 F 20160728 20160907 20160903 20160913 EXP US-AMGEN-USASP2016105931 AMGEN 32.00 YR A M Y 83.45000 KG 20160912 MD US US

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
127133822 12713382 1 PS REPATHA EVOLOCUMAB 1 Subcutaneous 140 UNK 125522 SOLUTION FOR INJECTION QOW
127133822 12713382 2 SS REPATHA EVOLOCUMAB 1 125522 SOLUTION FOR INJECTION
127133822 12713382 3 SS SIMVASTATIN. SIMVASTATIN 1 Unknown 40 UNK, QD 0 QD
127133822 12713382 4 C EZETIMIBE. EZETIMIBE 1 10 UNK, QD 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127133822 12713382 1 Type IIa hyperlipidaemia
127133822 12713382 2 Type IIa hyperlipidaemia
127133822 12713382 3 Type IIa hyperlipidaemia
127133822 12713382 4 Type IIa hyperlipidaemia

Outcome of event

Event ID CASEID OUTC COD
127133822 12713382 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127133822 12713382 Blood creatine phosphokinase increased

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
127133822 12713382 1 201603 0
127133822 12713382 3 200512 201608 0
127133822 12713382 4 200512 0