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
127415071 12741507 1 I 20160912 20160914 20160914 EXP CA-ROCHE-1829729 ROCHE 47.00 YR M Y 0.00000 20160914 OT CA CA

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
127415071 12741507 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous U 103964
127415071 12741507 2 SS RIBAVIRIN. RIBAVIRIN 1 Unknown U 21511
127415071 12741507 3 SS SOVALDI SOFOSBUVIR 1 Unknown U 0 400 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127415071 12741507 1 Hepatitis C
127415071 12741507 2 Hepatitis C
127415071 12741507 3 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
127415071 12741507 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127415071 12741507 Disease progression
127415071 12741507 Drug ineffective
127415071 12741507 Treatment failure

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found