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
122351523 12235152 3 F 20150125 20160805 20160404 20160809 EXP JP-JNJFOC-20150717703 JANSSEN 68.99 YR E F Y 44.00000 KG 20160809 OT JP JP

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
122351523 12235152 1 PS SOVRIAD SIMEPREVIR 1 Oral N 205123 100 MG CAPSULE QD
122351523 12235152 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral 0 600 MG UNSPECIFIED QD
122351523 12235152 3 SS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous 0 180 UG INJECTION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122351523 12235152 1 Chronic hepatitis C
122351523 12235152 2 Chronic hepatitis C
122351523 12235152 3 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
122351523 12235152 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122351523 12235152 Constipation
122351523 12235152 Haemoglobin decreased
122351523 12235152 Pruritus

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
122351523 12235152 1 20150123 20150417 0
122351523 12235152 2 20150123 20150710 0
122351523 12235152 3 20150123 20150703 0