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
126062991 12606299 1 I 2016 20160722 20160729 20160729 EXP US-AMGEN-USASP2016096345 AMGEN 47.00 YR A M Y 72.00000 KG 20160729 PH 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
126062991 12606299 1 PS PROCRIT ERYTHROPOIETIN 1 Subcutaneous 8000 UNIT, QWK Y 103234 UNKNOWN FORMULATION /wk
126062991 12606299 2 SS PROCRIT ERYTHROPOIETIN 1 Subcutaneous 6000 UNIT, QWK Y 103234 UNKNOWN FORMULATION /wk
126062991 12606299 3 SS PROCRIT ERYTHROPOIETIN 1 Subcutaneous 8000 UNIT, QWK Y 103234 UNKNOWN FORMULATION /wk
126062991 12606299 4 SS PROCRIT ERYTHROPOIETIN 1 Subcutaneous 7000 UNIT, QWK Y 103234 UNKNOWN FORMULATION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126062991 12606299 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126062991 12606299 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126062991 12606299 Cardiac disorder
126062991 12606299 Cytomegalovirus infection
126062991 12606299 Drug dose omission
126062991 12606299 Haemoglobin decreased
126062991 12606299 Hypertension
126062991 12606299 Incorrect product storage
126062991 12606299 Stress

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
126062991 12606299 1 201510 201603 0
126062991 12606299 2 201604 201605 0
126062991 12606299 3 201605 20160630 0
126062991 12606299 4 20160630 0