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
125476171 12547617 1 I 20120409 20130225 20160712 20160712 EXP DE-ROCHE-1791942 ROCHE 47.00 YR M Y 0.00000 20160712 MD DE DE

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
125476171 12547617 1 PS Peg-Interferon Alfa 2a PEGINTERFERON ALFA-2A 1 Unknown U 103964
125476171 12547617 2 SS RIBAVIRIN. RIBAVIRIN 1 Unknown U 21511

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125476171 12547617 1 Chronic hepatitis C
125476171 12547617 2 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125476171 12547617 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125476171 12547617 Anaemia
125476171 12547617 Chest discomfort
125476171 12547617 Cough
125476171 12547617 Fatigue
125476171 12547617 Haemorrhage subcutaneous
125476171 12547617 Headache
125476171 12547617 Leukopenia
125476171 12547617 Nausea
125476171 12547617 Pancytopenia
125476171 12547617 Skin disorder
125476171 12547617 Thrombocytopenia
125476171 12547617 Vertigo

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

no results found

Therapies reported

no results found