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
125321971 12532197 1 I 20140705 20150303 20160706 20160706 EXP JP-JNJFOC-20150317931 JANSSEN 57.00 YR A M Y 76.00000 KG 20160706 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
125321971 12532197 1 PS SOVRIAD SIMEPREVIR 1 Oral N 205123 100 MG CAPSULE QD
125321971 12532197 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral Y 0 800 MG UNKNOWN QD
125321971 12532197 3 SS RIBAVIRIN. RIBAVIRIN 1 Oral Y 0 600 MG UNKNOWN QD
125321971 12532197 4 SS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous 0 180 UG INJECTION /wk
125321971 12532197 5 C AMLODIN AMLODIPINE BESYLATE 1 Oral 0 10 MG TABLET QD
125321971 12532197 6 C URSODEOXYCHOLIC ACID URSODIOL 1 Oral 0 600 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125321971 12532197 1 Chronic hepatitis C
125321971 12532197 2 Chronic hepatitis C
125321971 12532197 3 Chronic hepatitis C
125321971 12532197 4 Chronic hepatitis C
125321971 12532197 5 Hypertension
125321971 12532197 6 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125321971 12532197 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125321971 12532197 Anaemia
125321971 12532197 Pyrexia
125321971 12532197 White blood cell 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
125321971 12532197 1 20140705 20140926 0
125321971 12532197 2 20140705 20140821 0
125321971 12532197 3 20140822 20141219 0
125321971 12532197 4 20140705 20141212 0
125321971 12532197 6 20140704 0