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
114873632 11487363 2 F 20160217 20150910 20160816 PER US-ROCHE-1311126 ROCHE 0.00 M Y 0.00000 20160816 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
114873632 11487363 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous PATIENT WAS ACTUALLY PRESCRIBED THIS DOSE FOR 1 WEEK ONLY 103964 90 UG /wk
114873632 11487363 2 SS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous DOSE 240 WAS STARTED 1 WEEK LATER TO 24/MAY/2013 103964 240 UG
114873632 11487363 3 SS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous PATIENT'S MOST RECENT ONGOING DOSE 103964 180 UG /wk
114873632 11487363 4 C JAKAFI RUXOLITINIB 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114873632 11487363 1 Polycythaemia vera

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
114873632 11487363 Arthralgia
114873632 11487363 Influenza like illness
114873632 11487363 Ocular neoplasm
114873632 11487363 Pruritus
114873632 11487363 Rash
114873632 11487363 Skin ulcer
114873632 11487363 Vision blurred
114873632 11487363 Visual impairment

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
114873632 11487363 1 20130524 20131016 0
114873632 11487363 2 20131016 0
114873632 11487363 3 20130526 0