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
119029742 11902974 2 F 20160101 20160202 20160108 20160805 PER US-ABBVIE-15P-163-1510148-00 ABBVIE 0.00 F Y 0.00000 20160805 CN US 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
119029742 11902974 1 PS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral UNKNOWN 206619
119029742 11902974 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral UNKNOWN 0
119029742 11902974 3 SS RIBAVIRIN. RIBAVIRIN 1 Oral DROP DOWN TO TWO IN THE AM AND TWO IN PM UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119029742 11902974 1 Hepatitis C
119029742 11902974 2 Hepatitis C

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
119029742 11902974 Decreased appetite
119029742 11902974 Depression
119029742 11902974 Diarrhoea
119029742 11902974 Dyspnoea
119029742 11902974 Fatigue
119029742 11902974 Gastrooesophageal reflux disease
119029742 11902974 Haemoglobin decreased
119029742 11902974 Insomnia
119029742 11902974 Iron deficiency
119029742 11902974 Malaise
119029742 11902974 Nausea
119029742 11902974 Thirst
119029742 11902974 Transfusion
119029742 11902974 Weight decreased

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
119029742 11902974 1 20151113 0
119029742 11902974 2 20151113 0