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
116822764 11682276 4 F 20151016 20160713 20151029 20160721 EXP CO-AMGEN-COLSL2015112714 AMGEN 79.00 YR E F Y 60.00000 KG 20160721 CN CO CO

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
116822764 11682276 1 PS NPLATE ROMIPLOSTIM 1 Subcutaneous 125 MUG, QWK 1057476 125268 125 UG SOLUTION FOR INJECTION /wk
116822764 11682276 2 SS NPLATE ROMIPLOSTIM 1 Subcutaneous 250 MUG, QWK 125268 250 UG SOLUTION FOR INJECTION /wk
116822764 11682276 3 SS NPLATE ROMIPLOSTIM 1 Subcutaneous 200 MUG, QWK 125268 200 UG SOLUTION FOR INJECTION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116822764 11682276 1 Immune thrombocytopenic purpura

Outcome of event

Event ID CASEID OUTC COD
116822764 11682276 OT
116822764 11682276 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
116822764 11682276 Biopsy lip
116822764 11682276 Decreased appetite
116822764 11682276 Diabetes mellitus
116822764 11682276 Diarrhoea
116822764 11682276 Ecchymosis
116822764 11682276 Headache
116822764 11682276 Hypothermia
116822764 11682276 Lip oedema
116822764 11682276 Petechiae
116822764 11682276 Thrombocytopenia

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
116822764 11682276 1 20150521 0