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
126093692 12609369 2 F 2014 20160802 20160801 20160809 EXP US-AMGEN-USASL2016097273 AMGEN 70.00 YR E M Y 0.00000 20160809 CN 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
126093692 12609369 1 PS NPLATE ROMIPLOSTIM 1 Unknown UNK U 125268 POWDER FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126093692 12609369 1 Immune thrombocytopenic purpura

Outcome of event

Event ID CASEID OUTC COD
126093692 12609369 OT
126093692 12609369 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126093692 12609369 Coronary artery occlusion
126093692 12609369 Groin abscess
126093692 12609369 Paraesthesia
126093692 12609369 Platelet count abnormal

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
126093692 12609369 1 2012 0