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
123476683 12347668 3 F 20160316 20160720 20160509 20160726 EXP FR-AMGEN-FRASP2016056841 AMGEN 35.00 YR A M Y 95.00000 KG 20160726 OT FR FR

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
123476683 12347668 1 PS NPLATE ROMIPLOSTIM 1 Intravenous (not otherwise specified) 10 MUG/KG, UNK 125268 10 UG/KG POWDER FOR INJECTION
123476683 12347668 2 C VELBE VINBLASTINE SULFATE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123476683 12347668 1 Immune thrombocytopenic purpura

Outcome of event

Event ID CASEID OUTC COD
123476683 12347668 HO
123476683 12347668 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123476683 12347668 Colitis ischaemic
123476683 12347668 Mesenteric vein thrombosis
123476683 12347668 Portal vein thrombosis
123476683 12347668 Thrombocytosis

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
123476683 12347668 1 20160310 20160310 0