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
125922172 12592217 2 F 20160710 20160916 20160726 20160927 EXP US-AMGEN-USASL2016093938 AMGEN 73.00 YR E F Y 0.00000 20160927 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
125922172 12592217 1 PS NPLATE ROMIPLOSTIM 1 Unknown UNK 125268 POWDER FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125922172 12592217 1 Immune thrombocytopenic purpura

Outcome of event

Event ID CASEID OUTC COD
125922172 12592217 OT
125922172 12592217 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125922172 12592217 Cellulitis
125922172 12592217 Diverticulitis
125922172 12592217 Gingival bleeding
125922172 12592217 Gingival discolouration
125922172 12592217 Hospitalisation
125922172 12592217 Immune thrombocytopenic purpura
125922172 12592217 Internal haemorrhage
125922172 12592217 Muscle rupture
125922172 12592217 Platelet count abnormal

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found