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
125411092 12541109 2 F 201606 20160706 20160708 20160712 EXP MX-009507513-1607MEX002428 MERCK 59.00 YR F Y 60.00000 KG 20160712 OT MX MX

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
125411092 12541109 1 PS PEGINTERFERON ALFA-2B PEGINTERFERON ALFA-2B 1 Subcutaneous STRENGTH: 100 MCG; 0.4 ML, QW 103949 .4 ML POWDER FOR INJECTION /wk
125411092 12541109 2 SS COTRONAK RIBAVIRIN 1 Oral 800 MG, QD (4 TABLETS PER DAY) 0 800 MG CAPSULE QD
125411092 12541109 3 C INSULIN GLARGINE INSULIN GLARGINE 1 Subcutaneous APPROXIMATELY A YEAR AND A HALF; TOTAL DAILY DOSE: 1 DOSE DAILY (1 DOSE EVERY 24 HOURS)) U 0 1 DF INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125411092 12541109 1 Hepatitis C
125411092 12541109 2 Hepatitis C
125411092 12541109 3 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125411092 12541109 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125411092 12541109 Anaemia
125411092 12541109 Arthralgia
125411092 12541109 Asterixis
125411092 12541109 Chills
125411092 12541109 Malaise
125411092 12541109 Myalgia
125411092 12541109 Pyrexia

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
125411092 12541109 1 20160602 0
125411092 12541109 2 20160602 0