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
126706161 12670616 1 I 20160810 20160822 20160822 EXP CH-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-067055 BRISTOL MYERS SQUIBB 53.00 YR M Y 0.00000 20160822 OT CH CH

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
126706161 12670616 1 PS STAVUDINE. STAVUDINE 1 Unknown UNK 20412
126706161 12670616 2 SS INDINAVIR INDINAVIR 1 Unknown UNK 0
126706161 12670616 3 SS LAMIVUDINE. LAMIVUDINE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126706161 12670616 1 HIV infection
126706161 12670616 2 HIV infection
126706161 12670616 3 HIV infection

Outcome of event

Event ID CASEID OUTC COD
126706161 12670616 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126706161 12670616 Viral mutation identified
126706161 12670616 Virologic failure

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
126706161 12670616 1 1997 0
126706161 12670616 2 1997 0
126706161 12670616 3 1997 0