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
124847952 12484795 2 F 20160729 20160621 20160808 PER US-009507513-1606USA009641 MERCK 0.00 Y 0.00000 20160808 CN US US

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
124847952 12484795 1 PS REBETOL RIBAVIRIN 1 800 MG, QD 20903 800 MG CAPSULE QD
124847952 12484795 2 SS REBETOL RIBAVIRIN 1 20903 CAPSULE
124847952 12484795 3 SS ABT-493 GLECAPREVIR 1 300 MG, QD 0 300 MG QD
124847952 12484795 4 SS ABT-493 GLECAPREVIR 1 0
124847952 12484795 5 SS ABT-530 PIBRENTASVIR 1 120 MG, QD 0 120 MG QD
124847952 12484795 6 SS ABT-530 PIBRENTASVIR 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124847952 12484795 1 Hepatic cirrhosis
124847952 12484795 2 Hepatitis C
124847952 12484795 3 Hepatic cirrhosis
124847952 12484795 4 Hepatitis C
124847952 12484795 5 Hepatic cirrhosis
124847952 12484795 6 Hepatitis C

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124847952 12484795 Fatigue
124847952 12484795 Headache
124847952 12484795 Nausea

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

no results found

Therapies reported

no results found