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
124708682 12470868 2 F 20160509 20160713 20160616 20160714 EXP RO-ROCHE-1762587 ROCHE 61.32 YR F Y 90.00000 KG 20160714 MD RO RO

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
124708682 12470868 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous Y 103964 180 UG SOLUTION FOR INJECTION /wk
124708682 12470868 2 SS MODERIBA RIBAVIRIN 1 Oral Y 0 600 MG BID
124708682 12470868 3 C ALGOCALMIN METAMIZOLE SODIUM 1 Intravenous (not otherwise specified) 1 VIAL 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124708682 12470868 1 Hepatitis C
124708682 12470868 2 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
124708682 12470868 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124708682 12470868 Malaise
124708682 12470868 Nausea
124708682 12470868 Rash
124708682 12470868 Vomiting

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
124708682 12470868 1 20160509 20160509 0
124708682 12470868 2 20160509 20160510 0
124708682 12470868 3 20160509 20160510 0