The Safety Rates Drug Report

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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
127715901 12771590 1 I 20160629 20160922 20160922 PER US-AMGEN-USASP2016085568 AMGEN 0.00 F Y 0.00000 20160922 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
127715901 12771590 1 PS NEULASTA PEGFILGRASTIM 1 Unknown UNK U 125031 UNKNOWN FORMULATION
127715901 12771590 2 SS NEUPOGEN FILGRASTIM 1 Unknown UNK U 0 UNKNOWN FORMULATION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127715901 12771590 1 Neutropenia
127715901 12771590 2 Neutropenia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127715901 12771590 Drug ineffective

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found