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
125228061 12522806 1 I 20160623 20160701 20160701 EXP AU-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-052722 BRISTOL MYERS SQUIBB 50.00 YR M Y 0.00000 20160701 CN AU AU

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
125228061 12522806 1 PS EFAVIRENZ EFAVIRENZ 1 Unknown UNK U 20972
125228061 12522806 2 SS COMBIVIR LAMIVUDINEIDOVUDINE 1 Unknown UNK Y 0
125228061 12522806 3 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Unknown U 0
125228061 12522806 4 SS DOLUTEGRAVIR DOLUTEGRAVIR 1 Unknown UNK Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125228061 12522806 1 Product used for unknown indication
125228061 12522806 2 Product used for unknown indication
125228061 12522806 3 Product used for unknown indication
125228061 12522806 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125228061 12522806 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125228061 12522806 Depression
125228061 12522806 Lipodystrophy acquired
125228061 12522806 Myalgia
125228061 12522806 Neuropathy peripheral

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

no results found

Therapies reported

no results found