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
126416181 12641618 1 I 20160706 20160807 20160810 20160810 EXP RO-ABBVIE-16P-135-1696151-00 ABBVIE 61.56 YR F Y 0.00000 20160810 CN COUNTRY NOT SPECIFIED RO

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
126416181 12641618 1 PS VIEKIRAX OMBITASVIRPARITAPREVIRRITONAVIR 1 Oral 2-0-0: 2 IN THE MORNING 1060132 206619 FILM-COATED TABLET
126416181 12641618 2 SS VIEKIRAX OMBITASVIRPARITAPREVIRRITONAVIR 1 1060132 206619
126416181 12641618 3 SS EXVIERA DASABUVIR 1 Oral 1-0-1: 1 IN THE MORNING AND 1 IN THE EVENING 1059033 206619 FILM-COATED TABLET
126416181 12641618 4 SS EXVIERA DASABUVIR 1 1059033 206619
126416181 12641618 5 SS REBETOL RIBAVIRIN 1 Oral Y UNKNOWN 0 CAPSULE BID
126416181 12641618 6 SS REBETOL RIBAVIRIN 1 Y UNKNOWN 0
126416181 12641618 7 C URSOFALK URSODIOL 1 Oral 0 CAPSULE TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126416181 12641618 1 Hepatitis C
126416181 12641618 2 Hepatic cirrhosis
126416181 12641618 3 Hepatitis C
126416181 12641618 4 Hepatic cirrhosis
126416181 12641618 5 Hepatitis C
126416181 12641618 6 Hepatic cirrhosis
126416181 12641618 7 Liver disorder

Outcome of event

Event ID CASEID OUTC COD
126416181 12641618 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126416181 12641618 Asthenia
126416181 12641618 Decreased appetite
126416181 12641618 Headache
126416181 12641618 Hyperbilirubinaemia
126416181 12641618 Hypoalbuminaemia
126416181 12641618 Nausea
126416181 12641618 Oedema peripheral

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
126416181 12641618 1 20160704 0
126416181 12641618 3 20160704 0
126416181 12641618 5 20160704 20160708 0
126416181 12641618 7 20160708 0