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
125331101 12533110 1 I 20150819 20160628 20160706 20160706 EXP US-ABBVIE-16P-163-1669463-00 ABBVIE 56.00 YR F 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
125331101 12533110 1 PS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral UNKNOWN 206619
125331101 12533110 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125331101 12533110 1 Chronic hepatitis C
125331101 12533110 2 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125331101 12533110 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125331101 12533110 Constipation
125331101 12533110 Gastrointestinal haemorrhage
125331101 12533110 Pruritus
125331101 12533110 Upper respiratory tract infection

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
125331101 12533110 1 20150818 20151110 0
125331101 12533110 2 20150818 20150823 0