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
127223891 12722389 1 I 20160620 20160905 20160907 20160907 EXP IT-ABBVIE-16P-083-1719708-00 ABBVIE 73.69 YR F Y 0.00000 20160907 PH 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
127223891 12722389 1 PS VIEKIRAX OMBITASVIRPARITAPREVIRRITONAVIR 1 Oral UNKNOWN 206619 TABLET QD
127223891 12722389 2 SS EXVIERA DASABUVIR 1 Oral UNKNOWN 206619 TABLET QD
127223891 12722389 3 SS REBETOL RIBAVIRIN 1 Oral UNKNOWN 0 200 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127223891 12722389 1 Chronic hepatitis C
127223891 12722389 2 Chronic hepatitis C
127223891 12722389 3 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
127223891 12722389 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127223891 12722389 Asthenia
127223891 12722389 Hyperhidrosis
127223891 12722389 Nausea
127223891 12722389 Weight decreased

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
127223891 12722389 1 20160620 0
127223891 12722389 2 20160620 0
127223891 12722389 3 20160620 0