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
124489013 12448901 3 F 20151226 20160908 20160608 20160916 EXP US-AMGEN-USASL2016024600 AMGEN 69.00 YR E M Y 0.00000 20160916 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
124489013 12448901 1 PS NPLATE ROMIPLOSTIM 1 Unknown 425 MCG, QWK N 125268 425 UG POWDER FOR INJECTION /wk
124489013 12448901 2 SS NPLATE ROMIPLOSTIM 1 Unknown 225 MCG, UNK N 125268 225 UG POWDER FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124489013 12448901 1 Immune thrombocytopenic purpura

Outcome of event

Event ID CASEID OUTC COD
124489013 12448901 HO
124489013 12448901 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124489013 12448901 Chest tube removal
124489013 12448901 Coronary artery bypass
124489013 12448901 Drug effect delayed
124489013 12448901 Fall
124489013 12448901 Foot fracture
124489013 12448901 Lung disorder
124489013 12448901 Mole excision
124489013 12448901 Neuropathy peripheral
124489013 12448901 Platelet count abnormal
124489013 12448901 Platelet count decreased
124489013 12448901 Platelet count increased
124489013 12448901 Pulmonary air leakage
124489013 12448901 Thoracostomy

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
124489013 12448901 1 20111031 0
124489013 12448901 2 20160903 0