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
125923421 12592342 1 I 20160412 20160721 20160726 20160726 EXP IT-ROCHE-1801349 ROCHE 55.91 YR F Y 0.00000 20160726 PH 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
125923421 12592342 1 PS COPEGUS RIBAVIRIN 1 Oral DAILY 21511 800 MG FILM-COATED TABLET QD
125923421 12592342 2 SS SOVALDI SOFOSBUVIR 1 Oral DAILY 0 400 MG FILM-COATED TABLET QD
125923421 12592342 3 SS DAKLINZA DACLATASVIR 1 Oral DAILY 0 60 MG FILM-COATED TABLET QD
125923421 12592342 4 C XANAX ALPRAZOLAM 1 Oral 0 .25 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125923421 12592342 1 Hepatitis C
125923421 12592342 2 Hepatitis C
125923421 12592342 3 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125923421 12592342 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125923421 12592342 Drug ineffective
125923421 12592342 Hepatitis C RNA

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
125923421 12592342 1 20150924 20160302 0
125923421 12592342 2 20150924 20160302 0
125923421 12592342 3 20150924 20160302 0
125923421 12592342 4 20150924 0