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
125740271 12574027 1 I 2016 20160713 20160720 20160720 EXP US-AMGEN-USASL2016091284 AMGEN 67.00 YR E F Y 0.00000 20160720 CN 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
125740271 12574027 1 PS REPATHA EVOLOCUMAB 1 Unknown UNK UNK, Q2WK Y 1067507 125522 SOLUTION FOR INJECTION QOW
125740271 12574027 2 SS REPATHA EVOLOCUMAB 1 Y 125522 SOLUTION FOR INJECTION
125740271 12574027 3 SS ATORVASTATIN ATORVASTATIN 1 Unknown 0
125740271 12574027 4 C METOPROLOL. METOPROLOL 1 0
125740271 12574027 5 C LISINOPRIL. LISINOPRIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125740271 12574027 1 Hyperlipidaemia
125740271 12574027 2 Blood triglycerides increased
125740271 12574027 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125740271 12574027 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125740271 12574027 Breast cancer
125740271 12574027 Fatigue
125740271 12574027 Hypotension
125740271 12574027 Injection site rash
125740271 12574027 Macule
125740271 12574027 Nausea
125740271 12574027 Neuropathy peripheral
125740271 12574027 Rash
125740271 12574027 Skin discolouration
125740271 12574027 Skin exfoliation
125740271 12574027 Swelling
125740271 12574027 Weight decreased

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
125740271 12574027 1 201604 0