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
124538337 12453833 7 F 20160331 20160809 20160609 20160810 EXP PL-AMGEN-POLCT2016072187 AMGEN 59.00 YR A M Y 75.00000 KG 20160810 MD PL PL

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
124538337 12453833 1 PS AMG 145 EVOLOCUMAB 1 Subcutaneous 420 MG, UNK N 125522 420 MG SOLUTION FOR INJECTION
124538337 12453833 2 SS Prefilled Autoinjector/Pen DEVICE 1 Subcutaneous UNK N 0 DEVICE
124538337 12453833 3 SS ATORVASTATIN ATORVASTATIN 1 Unknown 40 MG, UNK 0 40 MG
124538337 12453833 4 C NEBICARD NEBIVOLOL HYDROCHLORIDE 1 5 MG, QD 0 5 MG QD
124538337 12453833 5 C ACARD ASPIRIN 1 75 MG, QD 0 75 MG QD
124538337 12453833 6 C AREPLEX CLOPIDOGREL BISULFATE 1 5 MG, QD 0 5 MG QD
124538337 12453833 7 C AXTIL 2 1.25 UNK, QD 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124538337 12453833 1 Dyslipidaemia
124538337 12453833 2 Dyslipidaemia
124538337 12453833 3 Dyslipidaemia

Outcome of event

Event ID CASEID OUTC COD
124538337 12453833 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124538337 12453833 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
124538337 12453833 1 20140604 0
124538337 12453833 2 20140604 0
124538337 12453833 3 20140604 0