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
125688641 12568864 1 I 20160428 20160614 20160719 20160719 EXP IT-ROCHE-1776440 ROCHE 75.49 YR M Y 68.00000 KG 20160719 MD IT IT

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
125688641 12568864 1 PS COPEGUS RIBAVIRIN 1 Oral Y 21511 TABLET
125688641 12568864 2 SS SOVALDI SOFOSBUVIR 1 Oral Y 0 1 DF QD
125688641 12568864 3 C OMEPRAZOLE. OMEPRAZOLE 1 Oral 0 20 MG
125688641 12568864 4 C CATAPRESAN CLONIDINE 1 Transdermal 0 1 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125688641 12568864 1 Hepatitis C
125688641 12568864 2 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125688641 12568864 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125688641 12568864 Anaemia
125688641 12568864 Hepatitis C RNA increased
125688641 12568864 Treatment failure

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
125688641 12568864 1 20160108 20160428 0
125688641 12568864 2 20160108 20160428 0