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
95382802 9538280 2 F 20160712 20130920 20160714 EXP LS-BRISTOL-MYERS SQUIBB COMPANY-19219195 BRISTOL MYERS SQUIBB 59.00 YR M Y 0.00000 20160714 CN US LS

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
95382802 9538280 1 SS EFAVIRENZ EFAVIRENZ 1 Oral UNK U 0 CAPSULE
95382802 9538280 2 SS STAVUDINE. STAVUDINE 1 Unknown U 0
95382802 9538280 3 PS STREPTOMYCIN STREPTOMYCINSTREPTOMYCIN SULFATE 1 Unknown U 60108
95382802 9538280 4 SS LAMIVUDINE. LAMIVUDINE 1 Unknown U 0
95382802 9538280 5 SS ZIDOVUDINE. ZIDOVUDINE 1 Unknown U 0
95382802 9538280 6 SS NEVIRAPINE. NEVIRAPINE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
95382802 9538280 1 HIV infection
95382802 9538280 2 HIV infection
95382802 9538280 3 Product used for unknown indication
95382802 9538280 4 HIV infection
95382802 9538280 5 HIV infection
95382802 9538280 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
95382802 9538280 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
95382802 9538280 Drug resistance

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

no results found

Therapies reported

no results found