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
125688622 12568862 2 F 20160701 20160728 20160719 20160801 EXP IT-ROCHE-1796680 ROCHE 72.72 YR F Y 65.00000 KG 20160801 MD IT IT

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
125688622 12568862 1 PS COPEGUS RIBAVIRIN 1 Oral 21511 4 DF QD
125688622 12568862 2 SS SOVALDI SOFOSBUVIR 1 Oral 0 1 DF QD
125688622 12568862 3 C ESOMEPRAZOLE ESOMEPRAZOLE 1 Oral 0 1 DF
125688622 12568862 4 C NITROSYLON 2 Transdermal 0 1 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125688622 12568862 1 Hepatitis C
125688622 12568862 2 Hepatitis C
125688622 12568862 4 Hypertension

Outcome of event

Event ID CASEID OUTC COD
125688622 12568862 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125688622 12568862 Hepatitis C
125688622 12568862 Hepatitis C RNA increased
125688622 12568862 Treatment failure

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
125688622 12568862 1 20151208 20160524 0
125688622 12568862 2 20151208 20160524 0