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
125370322 12537032 2 F 20160714 20160707 20160715 EXP GB-ABBVIE-16P-167-1666464-00 ABBVIE 0.00 M Y 0.00000 20160715 OT COUNTRY NOT SPECIFIED GB

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
125370322 12537032 1 PS VIEKIRAX OMBITASVIRPARITAPREVIRRITONAVIR 1 Oral UNKNOWN 206619 TABLET
125370322 12537032 2 SS EXVIERA DASABUVIR 1 Oral UNKNOWN 206619 TABLET
125370322 12537032 3 SS RIBAVIRIN. RIBAVIRIN 1 Oral U UNKNOWN 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125370322 12537032 1 Hepatitis C
125370322 12537032 2 Hepatitis C
125370322 12537032 3 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125370322 12537032 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125370322 12537032 Abdominal distension
125370322 12537032 Deafness
125370322 12537032 Dry mouth
125370322 12537032 Dysgeusia
125370322 12537032 Emotional distress
125370322 12537032 Headache
125370322 12537032 Musculoskeletal pain
125370322 12537032 Pain in extremity
125370322 12537032 Rash

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
125370322 12537032 1 20160502 0
125370322 12537032 2 20160502 0