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
126273721 12627372 1 I 20160421 20160805 20160805 PER US-AMGEN-USASL2016051877 AMGEN 62.00 YR A M Y 0.00000 20160805 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
126273721 12627372 1 PS NPLATE ROMIPLOSTIM 1 Unknown UNK, QWK 125268 POWDER FOR INJECTION /wk
126273721 12627372 2 SS NPLATE ROMIPLOSTIM 1 Unknown UNK, Q3WK 125268 POWDER FOR INJECTION Q3W

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126273721 12627372 1 Immune thrombocytopenic purpura

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126273721 12627372 Drug ineffective
126273721 12627372 Off label use
126273721 12627372 Pain in extremity
126273721 12627372 Splenomegaly

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
126273721 12627372 1 201601 0