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
122310874 12231087 4 F 20160628 20160401 20160706 EXP US-AMGEN-USASL2016039007 AMGEN 70.00 YR E M Y 0.00000 20160706 CN 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
122310874 12231087 1 PS NPLATE ROMIPLOSTIM 1 Unknown UNK U 125268 POWDER FOR INJECTION
122310874 12231087 2 C PREDNISONE. PREDNISONE 1 5 MG AND 10 MG 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122310874 12231087 1 Immune thrombocytopenic purpura

Outcome of event

Event ID CASEID OUTC COD
122310874 12231087 HO
122310874 12231087 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122310874 12231087 Cardiac tamponade
122310874 12231087 Drug effect delayed
122310874 12231087 Fatigue
122310874 12231087 Infection
122310874 12231087 Myocardial infarction
122310874 12231087 Neoplasm malignant
122310874 12231087 Neuroendocrine carcinoma of the skin
122310874 12231087 Petechiae
122310874 12231087 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
122310874 12231087 1 2012 0