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
125904462 12590446 2 F 20160713 20160922 20160725 20160926 EXP SK-ABBVIE-16P-260-1683646-00 ABBVIE 0.00 F Y 0.00000 20160926 MD SK SK

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
125904462 12590446 1 PS VIEKIRAX OMBITASVIRPARITAPREVIRRITONAVIR 1 Oral Y 1058715 206619 TABLET QD
125904462 12590446 2 SS EXVIERA DASABUVIR 1 Oral Y 1058576 206619 TABLET BID
125904462 12590446 3 SS RIBAVIRIN. RIBAVIRIN 1 Oral U U UNKNOWN 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125904462 12590446 1 Chronic hepatitis C
125904462 12590446 2 Chronic hepatitis C
125904462 12590446 3 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125904462 12590446 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125904462 12590446 Anaemia
125904462 12590446 Anuria
125904462 12590446 Asthenia
125904462 12590446 Blood pressure decreased
125904462 12590446 Cardiac failure
125904462 12590446 Dyspepsia
125904462 12590446 Dyspnoea
125904462 12590446 Fatigue
125904462 12590446 Mineral deficiency
125904462 12590446 Pallor
125904462 12590446 Syncope
125904462 12590446 Vertigo

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
125904462 12590446 1 20160701 20160713 0
125904462 12590446 2 20160701 20160713 0