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
126273712 12627371 2 F 20160818 20160805 20160827 EXP US-AMGEN-USASL2016093199 AMGEN 75.00 YR E F Y 0.00000 20160827 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
126273712 12627371 1 PS NPLATE ROMIPLOSTIM 1 Unknown UNK U 125268 POWDER FOR INJECTION
126273712 12627371 2 SS NPLATE ROMIPLOSTIM 1 Unknown UNK, U 125268 POWDER FOR INJECTION QOW
126273712 12627371 3 C VITAMINS VITAMINS 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126273712 12627371 1 Immune thrombocytopenic purpura

Outcome of event

Event ID CASEID OUTC COD
126273712 12627371 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126273712 12627371 Contusion
126273712 12627371 Headache
126273712 12627371 Musculoskeletal disorder
126273712 12627371 Neck pain
126273712 12627371 Platelet count decreased
126273712 12627371 Urinary tract infection

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
126273712 12627371 1 2015 0
126273712 12627371 2 2015 0