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
126273381 12627338 1 I 2009 20151202 20160805 20160805 PER US-AMGEN-USASL2015129137 AMGEN 51.00 YR A F Y 122.45000 KG 20160805 OT 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
126273381 12627338 1 PS NPLATE ROMIPLOSTIM 1 Unknown UNK UNK, Q2WK 125268 POWDER FOR INJECTION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126273381 12627338 1 Immune thrombocytopenic purpura

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126273381 12627338 Headache
126273381 12627338 Myalgia

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
126273381 12627338 1 200902 0