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
123800932 12380093 2 F 20160427 20160627 20160518 20160701 EXP US-AMGEN-USASL2016062606 AMGEN 96.00 YR E F Y 74.83000 KG 20160701 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
123800932 12380093 1 PS PROCRIT ERYTHROPOIETIN 1 Subcutaneous 30000 UNIT, QWK 6262420A 103234 UNKNOWN FORMULATION /wk
123800932 12380093 2 SS PROCRIT ERYTHROPOIETIN 1 Subcutaneous UNK 6262418A 103234 UNKNOWN FORMULATION
123800932 12380093 3 SS EPOGEN ERYTHROPOIETIN 1 Unknown UNK 103234 UNKNOWN FORMULATION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123800932 12380093 1 Anaemia
123800932 12380093 3 Anaemia

Outcome of event

Event ID CASEID OUTC COD
123800932 12380093 DE
123800932 12380093 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123800932 12380093 Asthenia
123800932 12380093 Confusional state
123800932 12380093 Death
123800932 12380093 Dyspnoea
123800932 12380093 Living in residential institution

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
123800932 12380093 1 201510 0