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
126274001 12627400 1 I 2016 20160712 20160805 20160805 PER US-AMGEN-USASL2016090720 AMGEN 62.00 YR A F Y 0.00000 20160805 MD 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
126274001 12627400 1 PS NPLATE ROMIPLOSTIM 1 Unknown UNK, Q2WK 125268 POWDER FOR INJECTION QOW
126274001 12627400 2 C PREDNISONE. PREDNISONE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126274001 12627400 1 Product used for unknown indication
126274001 12627400 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126274001 12627400 Contusion
126274001 12627400 Epistaxis
126274001 12627400 Fatigue
126274001 12627400 Inappropriate schedule of drug administration
126274001 12627400 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
126274001 12627400 1 201605 0