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
126918501 12691850 1 I 20160817 20160819 20160827 20160827 EXP CO-AMGEN-COLSL2016110511 AMGEN 57.00 YR A F Y 43.00000 KG 20160826 OT CO CO

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
126918501 12691850 1 PS NPLATE ROMIPLOSTIM 1 Subcutaneous 120 MCG, QWK 336 UG Y 125268 120 UG SOLUTION FOR INJECTION /wk
126918501 12691850 2 C LEVOTHYROXINE. LEVOTHYROXINE 1 Unknown 175 MCG, UNK 0 175 UG
126918501 12691850 3 C PREDNISOLONE. PREDNISOLONE 1 Unknown 16 MG, UNK 0 16 MG
126918501 12691850 4 C OMEPRAZOLE. OMEPRAZOLE 1 Unknown 0
126918501 12691850 5 C FOLIC ACID. FOLIC ACID 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126918501 12691850 1 Thrombocytopenic purpura

Outcome of event

Event ID CASEID OUTC COD
126918501 12691850 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126918501 12691850 Thrombocytosis

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
126918501 12691850 1 20160804 20160818 0