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
126079971 12607997 1 I 20160725 20160726 20160729 20160729 EXP CO-JNJFOC-20160724820 JANSSEN 61.08 YR A M Y 76.00000 KG 20160729 OT CO CO

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
126079971 12607997 1 PS OLYSIO SIMEPREVIR 1 Oral N 205123 150 MG CAPSULE QD
126079971 12607997 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral Y 0 800 MG UNSPECIFIED QD
126079971 12607997 3 SS RIBAVIRIN. RIBAVIRIN 1 Oral Y 0 1200 MG UNSPECIFIED QD
126079971 12607997 4 C INTERFERON ALFA-2A INTERFERON ALFA-2A 1 Subcutaneous 0 180 UG INJECTION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126079971 12607997 1 Hepatitis C
126079971 12607997 2 Hepatitis C
126079971 12607997 3 Hepatitis C
126079971 12607997 4 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
126079971 12607997 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126079971 12607997 Haemoglobin 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
126079971 12607997 1 20160603 0
126079971 12607997 2 20160725 0
126079971 12607997 3 20160603 20160724 0
126079971 12607997 4 20160603 0