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
121966954 12196695 4 F 20151204 20160629 20160321 20160701 EXP AU-ABBVIE-16P-008-1538622-00 ABBVIE 62.18 YR M Y 0.00000 20160701 OT COUNTRY NOT SPECIFIED AU

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
121966954 12196695 1 PS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral 200MGS X3MANE X2 NOCTE UNKNOWN 206619
121966954 12196695 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral 200MGS X3MANE X2 NOCTE 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121966954 12196695 1 Hepatitis C
121966954 12196695 2 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
121966954 12196695 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121966954 12196695 Balance disorder
121966954 12196695 Dizziness
121966954 12196695 Fatigue
121966954 12196695 Feeling abnormal
121966954 12196695 Headache
121966954 12196695 Hepatic pain
121966954 12196695 Insomnia
121966954 12196695 Lethargy
121966954 12196695 Nausea
121966954 12196695 Suicidal ideation
121966954 12196695 Tinnitus
121966954 12196695 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
121966954 12196695 1 20151204 20160225 0
121966954 12196695 2 20151204 20160225 0