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
125965443 12596544 3 F 20160404 20160912 20160727 20160914 EXP IT-ROCHE-1802331 ROCHE 58.04 YR M Y 0.00000 20160914 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
125965443 12596544 1 PS COPEGUS RIBAVIRIN 1 Oral 21511 FILM-COATED TABLET
125965443 12596544 2 SS VIEKIRAX OMBITASVIRPARITAPREVIRRITONAVIR 1 Oral 0 FILM-COATED TABLET
125965443 12596544 3 C LASIX FUROSEMIDE 1 Oral 0 25 MG QD
125965443 12596544 4 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Oral 0 20 MG QD
125965443 12596544 5 C LAEVOLAC LACTULOSE 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125965443 12596544 1 Hepatitis C
125965443 12596544 2 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125965443 12596544 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125965443 12596544 Drug ineffective
125965443 12596544 Hepatitis C RNA

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
125965443 12596544 1 20151014 20160404 0
125965443 12596544 2 20151014 20160404 0