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
126058331 12605833 1 I 20160513 20160727 20160729 20160729 EXP IT-ROCHE-1804399 ROCHE 75.00 YR M Y 68.00000 KG 20160729 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
126058331 12605833 1 PS COPEGUS RIBAVIRIN 1 Oral Y 21511 4 DF QD
126058331 12605833 2 SS SOVALDI SOFOSBUVIR 1 Oral Y 0 TABLET
126058331 12605833 3 C OMEPRAZOLE. OMEPRAZOLE 1 0
126058331 12605833 4 C CATAPRESAN CLONIDINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126058331 12605833 1 Hepatitis C
126058331 12605833 2 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
126058331 12605833 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126058331 12605833 Anaemia
126058331 12605833 Drug ineffective
126058331 12605833 Hepatitis C
126058331 12605833 Hepatitis C RNA increased

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
126058331 12605833 1 20160108 0
126058331 12605833 2 20160108 0