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
125960202 12596020 2 F 201605 20160516 20160726 20160922 PER US-AMGEN-USASL2016062633 AMGEN 76.00 YR E M 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
125960202 12596020 1 PS KYPROLIS CARFILZOMIB 1 Unknown UNK U 202714 INTRAVENOUS INFUSION
125960202 12596020 2 SS NEUPOGEN FILGRASTIM 1 Unknown UNK U 0 UNKNOWN FORMULATION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125960202 12596020 1 Plasma cell myeloma
125960202 12596020 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125960202 12596020 Arthritis
125960202 12596020 Chest discomfort
125960202 12596020 Condition aggravated
125960202 12596020 Dyspnoea
125960202 12596020 Fatigue
125960202 12596020 Incorrect product storage

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
125960202 12596020 1 20160509 0
125960202 12596020 2 20160509 0