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
126182811 12618281 1 I 20160801 0 20160802 20160802 DIR 61.00 YR M N 0.00000 20160801 N OT 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
126182811 12618281 1 PS SOVALDI SOFOSBUVIR 1 N D 0
126182811 12618281 2 SS RIBASPHERE RIBAVIRIN 1 N D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126182811 12618281 1 Chronic hepatitis C
126182811 12618281 2 Chronic hepatitis C

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126182811 12618281 Fatigue
126182811 12618281 Headache

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

Event ID CASEID RPSR COD
126182811 12618281 HP

Therapies reported

no results found