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
125506911 12550691 1 I 20160707 20160712 20160712 EXP US-BAUSCH-BL-2016-016606 BAUSCH AND LOMB LAWITZ E, POORDAD F, WELLS J, HYLAND R, YANG Y, DVORY-SOBOL H, STAMM L, BRAINARD D, MCHUTCHISON J, LANDAVERDE C, GUTIERREZ J. HIGH EFFICACY OF SOFOSBUVIR/VELPATASVIR/GS-9857 WITH OR WITHOUT RIBAVIRIN FOR 12 WEEKS IN DIRECT-ACTING ANTIVIRAL-EXPERIENCED PATIENTS WITH GENOTYPE 1 HCV INFECTION. THE INTERNATIONAL LIVER CONGRESS. 2016;. 61.00 YR Y 0.00000 20160712 OT US 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
125506911 12550691 1 PS RIBAVIRIN. RIBAVIRIN 1 Unknown U 18859
125506911 12550691 2 SS SOFOSBUVIR SOFOSBUVIR 1 Oral U 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125506911 12550691 1 Hepatitis C
125506911 12550691 2 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125506911 12550691 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125506911 12550691 Hepatitis C

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

no results found

Therapies reported

no results found