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
126436553 12643655 3 F 20160501 20160915 20160811 20160923 EXP FR-AMGEN-FRASP2016101657 AMGEN 10.00 YR C M Y 41.00000 KG 20160922 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
126436553 12643655 1 PS NPLATE ROMIPLOSTIM 1 Subcutaneous 7 MCG/KG, QWK 826.622986 UG/KG Y 125268 7 UG/KG POWDER FOR INJECTION /wk
126436553 12643655 2 C ELTROMBOPAG ELTROMBOPAG 1 UNK 0
126436553 12643655 3 C VINBLASTINE VINBLASTINE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126436553 12643655 1 Immune thrombocytopenic purpura

Outcome of event

Event ID CASEID OUTC COD
126436553 12643655 HO
126436553 12643655 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126436553 12643655 Drug ineffective
126436553 12643655 Haemarthrosis
126436553 12643655 Immune thrombocytopenic purpura

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
126436553 12643655 1 20140201 20160625 0