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
126024782 12602478 2 F 20160802 20160728 20160802 EXP TW-ROCHE-1803156 ROCHE 68.00 YR F Y 0.00000 20160802 CN TW TW

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
126024782 12602478 1 PS RIBAVIRIN. RIBAVIRIN 1 Unknown U 21511
126024782 12602478 2 SS Peg-Interferon Alfa 2a PEGINTERFERON ALFA-2A 1 Unknown U 103964

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126024782 12602478 1 Hepatitis C
126024782 12602478 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126024782 12602478 HO
126024782 12602478 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126024782 12602478 Alopecia
126024782 12602478 Ascites
126024782 12602478 Depression
126024782 12602478 Drug ineffective
126024782 12602478 Fatigue
126024782 12602478 Hepatic neoplasm
126024782 12602478 Hypoaesthesia
126024782 12602478 Pain in extremity
126024782 12602478 Peritonitis bacterial
126024782 12602478 Pyrexia
126024782 12602478 Weight decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found