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
125383301 12538330 1 I 20151106 20160628 20160707 20160707 EXP US-ABBVIE-16P-163-1670881-00 ABBVIE 67.00 YR M Y 0.00000 20160707 OT COUNTRY NOT SPECIFIED 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
125383301 12538330 1 PS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral UNKNOWN 206619
125383301 12538330 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral UNKNOWN 0
125383301 12538330 3 SS RIBAVIRIN. RIBAVIRIN 1 Oral UNKNOWN 0 QOD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125383301 12538330 1 Chronic hepatitis C
125383301 12538330 2 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125383301 12538330 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125383301 12538330 Arthralgia
125383301 12538330 Decreased appetite
125383301 12538330 Depression
125383301 12538330 Feeling abnormal
125383301 12538330 Mood swings
125383301 12538330 Palpitations
125383301 12538330 Pruritus
125383301 12538330 Suicidal ideation
125383301 12538330 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
125383301 12538330 1 20151020 20160111 0
125383301 12538330 2 20151020 20151211 0
125383301 12538330 3 20151212 20160111 0