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
127591561 12759156 1 I 20160623 20160623 20160919 20160919 EXP CO-AMGEN-COLSL2016083032 AMGEN 38.00 YR A M Y 0.00000 20160919 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
127591561 12759156 1 PS NPLATE ROMIPLOSTIM 1 Subcutaneous 750 MUG, QWK Y 125268 750 UG SOLUTION FOR INJECTION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127591561 12759156 1 Immune thrombocytopenic purpura

Outcome of event

Event ID CASEID OUTC COD
127591561 12759156 HO
127591561 12759156 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127591561 12759156 Eye haemorrhage
127591561 12759156 Haematoma
127591561 12759156 Mouth haemorrhage
127591561 12759156 Thrombocytopenia
127591561 12759156 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
127591561 12759156 1 20160422 0