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
88809052 8880905 2 F 20120607 20160719 20121101 20160728 EXP GB-AMGEN-GBRSP2012045429 AMGEN 0.00 DY F Y 0.00000 20160728 MD GB GB

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
88809052 8880905 1 PS NPLATE ROMIPLOSTIM 1 Transplacental 650 MUG, QWK 39650 UG U 125268 650 UG UNKNOWN FORMULATION /wk
88809052 8880905 2 SS NPLATE ROMIPLOSTIM 1 Transmammary 300 UNK, QWK 39650 UG U 125268 UNKNOWN FORMULATION /wk
88809052 8880905 3 C AZATHIOPRINE. AZATHIOPRINE 1 Transplacental 200 MG, QD 0 200 MG QD
88809052 8880905 4 C DEXAMETHASONE. DEXAMETHASONE 1 Transplacental 20 MG, QD 0 20 MG QD
88809052 8880905 5 C IV-GLOBULIN 2 Transplacental 70 G, QWK 0 70 G /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
88809052 8880905 1 Immune thrombocytopenic purpura
88809052 8880905 3 Immune thrombocytopenic purpura
88809052 8880905 4 Immune thrombocytopenic purpura
88809052 8880905 5 Immune thrombocytopenic purpura

Outcome of event

Event ID CASEID OUTC COD
88809052 8880905 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
88809052 8880905 Exposure during breast feeding
88809052 8880905 Platelet count decreased

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
88809052 8880905 1 20100909 20111102 0
88809052 8880905 2 20120612 20120712 0
88809052 8880905 3 20111110 20120607 0
88809052 8880905 4 20120531 20120605 0
88809052 8880905 5 20111117 20120531 0