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
126030941 12603094 1 I 20141205 20160310 20160728 20160728 EXP IT-009507513-1603ITA006405 MERCK 50.00 YR F Y 0.00000 20160728 OT IT IT

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
126030941 12603094 1 PS BOCEPREVIR BOCEPREVIR 1 Oral 800 MG, TID 105600 MG 202258 800 MG CAPSULE TID
126030941 12603094 2 SS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous 180 MG, QW 1917.16 MG 0 180 MG SOLUTION FOR INJECTION /wk
126030941 12603094 3 SS COPEGUS RIBAVIRIN 1 Oral 600 MG, BID 78000 MG 0 600 MG CAPSULE BID
126030941 12603094 4 SS COPEGUS RIBAVIRIN 1 Oral 600 MG, QD 78000 MG 0 600 MG CAPSULE QD
126030941 12603094 5 SS COPEGUS RIBAVIRIN 1 Oral 1000 MG, QD 78000 MG 0 CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126030941 12603094 1 Chronic hepatitis C
126030941 12603094 2 Chronic hepatitis C
126030941 12603094 3 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
126030941 12603094 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126030941 12603094 Anaemia
126030941 12603094 Migraine
126030941 12603094 Neutropenia

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
126030941 12603094 1 20141125 20150414 0
126030941 12603094 2 20141028 20150414 0
126030941 12603094 3 20141028 20141223 0
126030941 12603094 4 20141223 20150225 0
126030941 12603094 5 20150225 20150414 0