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
125228681 12522868 1 I 201605 20160519 20160701 20160701 EXP US-INCYTE CORPORATION-2016IN003038 INCYTE 81.75 YR M Y 80.73000 KG 20160701 MD 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
125228681 12522868 1 PS JAKAFI RUXOLITINIB 1 Oral 15 MG, BID U 202192 15 MG TABLET
125228681 12522868 2 SS JAKAFI RUXOLITINIB 1 Oral 5 MG, BID U 202192 5 MG TABLET
125228681 12522868 3 SS ALLOPURINOL. ALLOPURINOL 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125228681 12522868 1 Polycythaemia vera
125228681 12522868 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125228681 12522868 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125228681 12522868 Blister
125228681 12522868 Fatigue
125228681 12522868 Oedema peripheral
125228681 12522868 Pancytopenia
125228681 12522868 Splenomegaly

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
125228681 12522868 1 201504 0
125228681 12522868 2 20160406 0