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
126800181 12680018 1 I 20160822 0 20160823 20160823 DIR 65.00 YR M N 0.00000 20160822 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
126800181 12680018 1 PS SOVALDI SOFOSBUVIR 1 0
126800181 12680018 2 SS RIBASPHERE RIBAVIRIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126800181 12680018 1 Chronic hepatitis C
126800181 12680018 2 Chronic hepatitis C

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126800181 12680018 Asthenia
126800181 12680018 Fatigue

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

Event ID CASEID RPSR COD
126800181 12680018 HP

Therapies reported

no results found