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
126273981 12627398 1 I 20160407 20160805 20160805 PER US-AMGEN-USASL2016044987 AMGEN 66.00 YR E M Y 0.00000 20160805 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
126273981 12627398 1 PS NPLATE ROMIPLOSTIM 1 Unknown 2 MUG, Q2WK U 125268 2 UG POWDER FOR INJECTION QOW
126273981 12627398 2 C PREDNISONE. PREDNISONE 1 UNK 0
126273981 12627398 3 C CELLCEPT MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126273981 12627398 1 Immune thrombocytopenic purpura

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126273981 12627398 Basophil count increased
126273981 12627398 Laboratory test abnormal
126273981 12627398 Lymphocyte count decreased
126273981 12627398 Mean cell haemoglobin decreased
126273981 12627398 Monocyte count increased
126273981 12627398 Myelocyte count increased
126273981 12627398 Off label use
126273981 12627398 Platelet count abnormal
126273981 12627398 Red cell distribution width increased
126273981 12627398 White blood cell 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
126273981 12627398 1 20140101 0
126273981 12627398 2 1990 0