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
120013093 12001309 3 F 20151228 20160701 20160204 20160709 EXP US-AMGEN-USASL2015140941 AMGEN 53.00 YR A M Y 0.00000 20160709 OT 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
120013093 12001309 1 PS NPLATE ROMIPLOSTIM 1 Unknown UNK U 125268 POWDER FOR INJECTION
120013093 12001309 2 C RITUXAN RITUXIMAB 1 Unknown UNK 0
120013093 12001309 3 C PREDNISONE. PREDNISONE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120013093 12001309 1 Immune thrombocytopenic purpura

Outcome of event

Event ID CASEID OUTC COD
120013093 12001309 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120013093 12001309 Diverticulitis
120013093 12001309 Infection
120013093 12001309 Platelet count abnormal

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
120013093 12001309 1 20151101 0