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
123159412 12315941 2 F 20150701 20160626 20160428 20160701 EXP VN-BMSGILMSD-2016-0210281 GILEAD 45.00 YR A M Y 0.00000 20160701 OT VN VN

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
123159412 12315941 1 PS EFAVIRENZ/EMTRICITABINE/TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZEMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Unknown 1 DF, QD 21937 1 DF TABLET QD
123159412 12315941 2 SS PEGINTERFERON ALFA-2B PEGINTERFERON ALFA-2B 1 Subcutaneous 80 UG, Q1WK 3177.93091 UG N 0 80 UG /wk
123159412 12315941 3 SS RIBAVIRIN. RIBAVIRIN 1 Unknown 200 MG, BID 130800 MG N 0 200 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123159412 12315941 1 HIV infection
123159412 12315941 2 Hepatitis C
123159412 12315941 3 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
123159412 12315941 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123159412 12315941 Diabetes mellitus

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
123159412 12315941 1 20140329 0
123159412 12315941 2 20140808 20150701 0
123159412 12315941 3 20140808 20150701 0