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
125352441 12535244 1 I 201602 20160705 20160707 20160707 EXP FR-ROCHE-1789834 ROCHE 74.00 YR M Y 0.00000 20160707 MD FR FR

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
125352441 12535244 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous U 103964 45 UG /wk
125352441 12535244 2 SS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous U 103964 90 UG /wk
125352441 12535244 3 SS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous U 103964 135 UG /wk
125352441 12535244 4 C KARDEGIC ASPIRIN LYSINE 1 0
125352441 12535244 5 C SEROPLEX ESCITALOPRAM OXALATE 1 0
125352441 12535244 6 C JAKAFI RUXOLITINIB 1 Unknown 0 5 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125352441 12535244 1 Polycythaemia vera

Outcome of event

Event ID CASEID OUTC COD
125352441 12535244 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125352441 12535244 Depression

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
125352441 12535244 1 20160114 0
125352441 12535244 2 20160126 0
125352441 12535244 3 201602 20160302 0
125352441 12535244 6 20160325 0