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
94500893 9450089 3 F 201601 20160804 20130809 20160812 EXP US-AMGEN-USASP2013018121 AMGEN 55.00 YR A M Y 0.00000 20160812 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
94500893 9450089 1 PS NPLATE ROMIPLOSTIM 1 Unknown 90 UNK, LYOPHILIZED VIAL U 125268 POWDER FOR INJECTION
94500893 9450089 2 SS NPLATE ROMIPLOSTIM 1 Unknown 40 MUG, Q8WK U 125268 40 UG POWDER FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
94500893 9450089 1 Immune thrombocytopenic purpura

Outcome of event

Event ID CASEID OUTC COD
94500893 9450089 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
94500893 9450089 Asthenia
94500893 9450089 Cough
94500893 9450089 Deafness
94500893 9450089 Dysstasia
94500893 9450089 Ear discomfort
94500893 9450089 Fatigue
94500893 9450089 Immunosuppression
94500893 9450089 Influenza
94500893 9450089 Paraesthesia
94500893 9450089 Platelet count decreased
94500893 9450089 Productive cough
94500893 9450089 Rhinorrhoea
94500893 9450089 Skin lesion
94500893 9450089 Skin mass
94500893 9450089 Staphylococcal infection
94500893 9450089 Vertigo
94500893 9450089 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
94500893 9450089 1 201201 0