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
109829415 10982941 5 F 20140514 20160905 20150403 20160912 EXP JP-JNJFOC-20150322836 JANSSEN 63.09 YR A F Y 62.00000 KG 20160912 MD 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
109829415 10982941 1 PS SOVRIAD SIMEPREVIR 1 Oral N 205123 100 MG CAPSULE QD
109829415 10982941 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral 0 800 MG UNSPECIFIED QD
109829415 10982941 3 SS RIBAVIRIN. RIBAVIRIN 1 Oral 0 600 MG UNSPECIFIED QD
109829415 10982941 4 SS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous Y 0 180 UG INJECTION /wk
109829415 10982941 5 SS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous Y 0 144 UG INJECTION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109829415 10982941 1 Chronic hepatitis C
109829415 10982941 2 Chronic hepatitis C
109829415 10982941 3 Chronic hepatitis C
109829415 10982941 4 Chronic hepatitis C
109829415 10982941 5 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
109829415 10982941 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
109829415 10982941 Anaemia
109829415 10982941 Platelet count decreased

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
109829415 10982941 1 20140416 20140708 0
109829415 10982941 2 20140416 20140805 0
109829415 10982941 3 20140806 20141001 0
109829415 10982941 4 20140416 20140702 0
109829415 10982941 5 20140709 20141001 0