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
118995722 11899572 2 F 20160108 20160108 20160805 PER US-ABBVIE-15P-163-1471673-00 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
118995722 11899572 1 PS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral U UNKNOWN 206619 TABLET
118995722 11899572 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral U UNKNOWN 0 1000 MG
118995722 11899572 3 SS RIBAVIRIN. RIBAVIRIN 1 Oral U UNKNOWN 0 800 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118995722 11899572 1 Chronic hepatitis C
118995722 11899572 2 Hepatitis C

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118995722 11899572 Adverse drug reaction
118995722 11899572 Anxiety
118995722 11899572 Asthenia
118995722 11899572 Bedridden
118995722 11899572 Confusional state
118995722 11899572 Coordination abnormal
118995722 11899572 Decreased appetite
118995722 11899572 Depression
118995722 11899572 Dizziness
118995722 11899572 Fall
118995722 11899572 Fatigue
118995722 11899572 Feeling abnormal
118995722 11899572 Memory impairment
118995722 11899572 Nausea
118995722 11899572 Personality change
118995722 11899572 Sleep disorder
118995722 11899572 Stress
118995722 11899572 Tremor
118995722 11899572 Visual impairment
118995722 11899572 Vomiting

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found