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
125465881 12546588 1 I 20130522 20160420 20160711 20160711 EXP IL-009507513-1604ISR013494 MERCK 57.00 YR Y 0.00000 20160711 CN IL IL

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
125465881 12546588 1 SS RIBAVIRIN. RIBAVIRIN 1 Oral 1200 MG, QD 0 CAPSULE QD
125465881 12546588 2 PS BOCEPREVIR BOCEPREVIR 1 Unknown UNK 202258 CAPSULE
125465881 12546588 3 SS PEGINTERFERON ALFA-2A PEGINTERFERON ALFA-2A 1 Subcutaneous 180 MICROGRAM, QW 0 180 UG SOLUTION FOR INJECTION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125465881 12546588 1 Chronic hepatitis C
125465881 12546588 2 Hepatitis C
125465881 12546588 3 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125465881 12546588 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125465881 12546588 Anaemia
125465881 12546588 Asthenia
125465881 12546588 Erythema
125465881 12546588 Fatigue
125465881 12546588 Leukopenia
125465881 12546588 Pruritus
125465881 12546588 Rash

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
125465881 12546588 1 20130509 0
125465881 12546588 3 20130509 0