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
125776991 12577699 1 I 20160609 20160715 20160721 20160721 EXP IT-ROCHE-1796663 ROCHE 53.78 YR M Y 70.00000 KG 20160721 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
125776991 12577699 1 PS COPEGUS RIBAVIRIN 1 Oral 21511 4 DF QD
125776991 12577699 2 SS VIEKIRAX OMBITASVIRPARITAPREVIRRITONAVIR 1 Oral 0 2 DF QD
125776991 12577699 3 SS EXVIERA DASABUVIR 1 Oral 0 2 DF QD
125776991 12577699 4 C PANTORC PANTOPRAZOLE SODIUM 1 Oral 0
125776991 12577699 5 C CARDIOASPIRIN ASPIRIN 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125776991 12577699 1 Product used for unknown indication
125776991 12577699 2 Hepatitis C RNA
125776991 12577699 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125776991 12577699 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125776991 12577699 Hepatitis C RNA increased
125776991 12577699 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
125776991 12577699 1 20151104 20160420 0
125776991 12577699 2 20151104 20160420 0
125776991 12577699 3 20151104 20160420 0