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
122422422 12242242 2 F 20150209 20160824 20160406 20160830 EXP JP-JNJFOC-20160401209 JANSSEN 64.49 YR A M Y 34.02000 KG 20160830 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
122422422 12242242 1 PS SOVRIAD SIMEPREVIR 1 Oral N 205123 100 MG CAPSULE QD
122422422 12242242 2 SS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous 0 180 UG INJECTION /wk
122422422 12242242 3 SS RIBAVIRIN. RIBAVIRIN 1 Oral Y 0 600 MG UNSPECIFIED QD
122422422 12242242 4 SS RIBAVIRIN. RIBAVIRIN 1 Oral Y 0 800 MG UNSPECIFIED QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122422422 12242242 1 Chronic hepatitis C
122422422 12242242 2 Chronic hepatitis C
122422422 12242242 3 Chronic hepatitis C
122422422 12242242 4 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
122422422 12242242 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122422422 12242242 Anaemia
122422422 12242242 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
122422422 12242242 1 20150126 20150419 0
122422422 12242242 2 20150126 20150706 0
122422422 12242242 3 20150623 20150713 0
122422422 12242242 4 20150126 20150622 0