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
126070051 12607005 1 I 20160612 20160726 20160729 20160729 EXP ES-ABBVIE-16P-144-1686306-00 ABBVIE 78.00 YR F Y 0.00000 20160729 PH ES ES

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
126070051 12607005 1 PS VIEKIRAX OMBITASVIRPARITAPREVIRRITONAVIR 1 Oral Y UNKNOWN 206619 2 DF TABLET QD
126070051 12607005 2 SS VIEKIRAX OMBITASVIRPARITAPREVIRRITONAVIR 1 Y UNKNOWN 206619
126070051 12607005 3 SS EXVIERA DASABUVIR 1 Oral Y UNKNOWN 206619 250 MG TABLET Q12H
126070051 12607005 4 SS EXVIERA DASABUVIR 1 Y UNKNOWN 206619
126070051 12607005 5 SS RIBAVIRIN. RIBAVIRIN 1 Oral Y UNKNOWN 0 TABLET QD
126070051 12607005 6 SS RIBAVIRIN. RIBAVIRIN 1 Y UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126070051 12607005 1 Hepatitis C
126070051 12607005 2 Cryoglobulinaemia
126070051 12607005 3 Hepatitis C
126070051 12607005 4 Cryoglobulinaemia
126070051 12607005 5 Hepatitis C
126070051 12607005 6 Cryoglobulinaemia

Outcome of event

Event ID CASEID OUTC COD
126070051 12607005 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126070051 12607005 Abdominal pain upper
126070051 12607005 Asthenia
126070051 12607005 Blood bilirubin increased
126070051 12607005 Constipation

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
126070051 12607005 1 20160608 20160613 0
126070051 12607005 3 20160608 20160713 0