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
127468081 12746808 1 I 20160906 20160915 20160915 EXP SI-AMGEN-SVNSP2016123489 AMGEN 68.00 YR E F Y 0.00000 20160915 CN SI SI

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
127468081 12746808 1 PS NPLATE ROMIPLOSTIM 1 Unknown UNK, UNK U 125268 UNKNOWN FORMULATION
127468081 12746808 2 C IMMUNOGLOBULIN HUMAN IMMUNOGLOBULIN G 1 0
127468081 12746808 3 C DEXAMETHASONE. DEXAMETHASONE 1 0
127468081 12746808 4 C WARFARIN WARFARIN 1 0
127468081 12746808 5 C ELTROMBOPAG ELTROMBOPAG 1 25 MG, UNK 0 25 MG
127468081 12746808 6 C PREDNISONE. PREDNISONE 1 0
127468081 12746808 7 C RITUXIMAB RITUXIMAB 1 0
127468081 12746808 8 C VINBLASTINE VINBLASTINE 1 0
127468081 12746808 9 C VINCRISTINE VINCRISTINE 1 0
127468081 12746808 10 C DANAZOL. DANAZOL 1 0
127468081 12746808 11 C AZATHIOPRINE. AZATHIOPRINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127468081 12746808 1 Thrombocytopenia

Outcome of event

Event ID CASEID OUTC COD
127468081 12746808 OT
127468081 12746808 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127468081 12746808 Drug effect decreased
127468081 12746808 Haemoglobin decreased
127468081 12746808 Haemorrhage
127468081 12746808 Petechiae
127468081 12746808 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
127468081 12746808 1 201112 201311 0