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
125336951 12533695 1 I 20150520 20160628 20160706 20160706 EXP US-ABBVIE-16P-163-1669662-00 ABBVIE 69.00 YR M Y 0.00000 20160706 OT COUNTRY NOT SPECIFIED 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
125336951 12533695 1 PS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral UNKNOWN 206619
125336951 12533695 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral UNKNOWN 0
125336951 12533695 3 SS RIBAVIRIN. RIBAVIRIN 1 Oral UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125336951 12533695 1 Chronic hepatitis C
125336951 12533695 2 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125336951 12533695 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125336951 12533695 Anaemia
125336951 12533695 Blindness unilateral
125336951 12533695 Nausea
125336951 12533695 Retinal vascular occlusion
125336951 12533695 Sleep apnoea syndrome
125336951 12533695 Vomiting

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
125336951 12533695 1 20150519 20150811 0
125336951 12533695 2 20150619 20150712 0
125336951 12533695 3 20150713 20150811 0