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
124585362 12458536 2 F 20160418 20160707 20160613 20160714 EXP FR-AMGEN-FRASP2016054410 AMGEN 0.00 F Y 50.00000 KG 20160714 MD 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
124585362 12458536 1 PS NPLATE ROMIPLOSTIM 1 Subcutaneous 350 MUG, QWK 125268 350 UG POWDER FOR INJECTION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124585362 12458536 1 Immune thrombocytopenic purpura

Outcome of event

Event ID CASEID OUTC COD
124585362 12458536 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124585362 12458536 Drug effect decreased
124585362 12458536 Platelet count decreased

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
124585362 12458536 1 20131115 0