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
117746882 11774688 2 F 20151007 20160706 20151124 20160711 EXP IT-ABBVIE-15P-083-1504190-00 ABBVIE 54.09 YR M Y 81.00000 KG 20160711 MD IT IT

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
117746882 11774688 1 PS VIEKIRAX OMBITASVIRPARITAPREVIRRITONAVIR 1 Oral Y UNKNOWN 206619 COATED TABLET
117746882 11774688 2 SS EXVIERA DASABUVIR 1 Oral Y UNKNOWN 206619 COATED TABLET QD
117746882 11774688 3 SS COPEGUS RIBAVIRIN 1 Oral Y UNKNOWN 0 COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117746882 11774688 1 Hepatic cirrhosis
117746882 11774688 2 Hepatic cirrhosis
117746882 11774688 3 Hepatic cirrhosis

Outcome of event

Event ID CASEID OUTC COD
117746882 11774688 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
117746882 11774688 Ascites
117746882 11774688 Cellulitis
117746882 11774688 Peau d'orange
117746882 11774688 Sepsis

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
117746882 11774688 1 20150717 20151009 0
117746882 11774688 2 20150717 20151009 0
117746882 11774688 3 20150717 20151009 0