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
122939694 12293969 4 F 2016 20160803 20160422 20160812 EXP IL-AMGEN-ISRSL2016051121 AMGEN 27.00 YR A F Y 0.00000 20160812 OT IL IL

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
122939694 12293969 1 PS NPLATE ROMIPLOSTIM 1 Unknown 620 MUG, QWK Y 125268 620 UG POWDER FOR INJECTION /wk
122939694 12293969 2 C IMURAN AZATHIOPRINE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122939694 12293969 1 Immune thrombocytopenic purpura

Outcome of event

Event ID CASEID OUTC COD
122939694 12293969 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122939694 12293969 Leukopenia
122939694 12293969 Platelet count abnormal
122939694 12293969 Urinary tract infection

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
122939694 12293969 1 201402 0