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
127819621 12781962 1 I 2014 20160920 20160927 20160927 EXP US-AMGEN-USASP2016129077 AMGEN 64.00 YR A M Y 0.00000 20160926 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
127819621 12781962 1 PS NEUPOGEN FILGRASTIM 1 Unknown UNK U 103353 SOLUTION FOR INJECTION
127819621 12781962 2 SS NEUPOGEN FILGRASTIM 1 Unknown 480 MUG, 2 TIMES/WK (TWICE A WEEK) U 103353 480 UG SOLUTION FOR INJECTION BIW
127819621 12781962 3 SS NEUPOGEN FILGRASTIM 1 Unknown 960 MUG, 2 TIMES/WK (TWICE A WEEK) U 103353 960 UG SOLUTION FOR INJECTION BIW
127819621 12781962 4 SS NEUPOGEN FILGRASTIM 1 Unknown 480 MUG, UNK U 103353 480 UG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127819621 12781962 1 Autoimmune neutropenia

Outcome of event

Event ID CASEID OUTC COD
127819621 12781962 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127819621 12781962 Bone pain
127819621 12781962 Drug ineffective
127819621 12781962 Fatigue
127819621 12781962 Incorrect dose administered
127819621 12781962 Incorrect product storage
127819621 12781962 Myalgia
127819621 12781962 Neutrophil count decreased
127819621 12781962 Pyrexia
127819621 12781962 Stomatitis

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
127819621 12781962 1 2014 0
127819621 12781962 2 2016 0
127819621 12781962 3 2016 0
127819621 12781962 4 201609 0