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
114874392 11487439 2 F 20151230 20150910 20160816 PER US-ROCHE-1415998 ROCHE 0.00 F Y 0.00000 20160816 OT 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
114874392 11487439 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous U UNKNOWN 103964 45 UG /wk
114874392 11487439 2 SS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous 1 WEEKLY FOR 6 WEEKS U UNKNOWN 103964 45 UG /wk
114874392 11487439 3 SS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous U UNKNOWN 103964 45 UG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114874392 11487439 1 Hepatitis C
114874392 11487439 2 Polycythaemia vera

Outcome of event

Event ID CASEID OUTC COD
114874392 11487439 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
114874392 11487439 Anxiety
114874392 11487439 Blood glucose increased
114874392 11487439 Dermatitis allergic
114874392 11487439 Fatigue
114874392 11487439 Headache
114874392 11487439 Injection site rash
114874392 11487439 Myalgia
114874392 11487439 Nausea
114874392 11487439 Night sweats
114874392 11487439 Oedema
114874392 11487439 Pruritus
114874392 11487439 Rash
114874392 11487439 Rash pruritic
114874392 11487439 Swelling

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
114874392 11487439 1 20130421 0
114874392 11487439 2 20140513 0
114874392 11487439 3 20150228 0