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
127052881 12705288 1 I 20160830 0 20160831 20160831 DIR 57.00 YR F N 0.00000 20160830 N PH 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
127052881 12705288 1 PS DAKLINZA DACLATASVIR 1 Oral D D 0 60 MG QD
127052881 12705288 2 SS SOVALDI SOFOSBUVIR 1 Oral SOVALDI TAB 400MG - 400 DF PO QD D D 0 400 DF QD
127052881 12705288 3 SS RIBASPHERE RIBAVIRIN 1 Oral RIBASPHERE CAP 200MG - 200 DF - ORAL - 2AM AND 2PM 0 200 DF Q12H

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127052881 12705288 1 Chronic hepatitis C
127052881 12705288 2 Chronic hepatitis C

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127052881 12705288 Decreased appetite
127052881 12705288 Fatigue
127052881 12705288 Headache

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

Event ID CASEID RPSR COD
127052881 12705288 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127052881 12705288 1 20160616 0
127052881 12705288 2 20160616 0
127052881 12705288 3 20160711 0