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
117330963 11733096 3 F 20160810 20151113 20160811 EXP CA-ROCHE-1649243 ROCHE 55.00 YR M Y 0.00000 20160811 CN CA CA

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
117330963 11733096 1 PS Peg-Interferon Alfa 2a PEGINTERFERON ALFA-2A 1 Unknown 103964
117330963 11733096 2 SS COPEGUS RIBAVIRIN 1 Unknown 21511
117330963 11733096 3 SS SOFOSBUVIR SOFOSBUVIR 1 Oral 0 400 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117330963 11733096 1 Chronic hepatitis C
117330963 11733096 2 Chronic hepatitis C
117330963 11733096 3 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
117330963 11733096 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117330963 11733096 Drug ineffective
117330963 11733096 Hepatitis C
117330963 11733096 Treatment failure

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found