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
125432371 12543237 1 I 20151206 20160131 20160711 20160711 EXP PR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-052068 BRISTOL MYERS SQUIBB 0.00 DY F Y 1.70000 KG 20160711 OT PR PR

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
125432371 12543237 1 PS ATAZANAVIR SULFATE ATAZANAVIR SULFATE 1 Transplacental 1 DF, UNK 21567 1 DF QD
125432371 12543237 2 SS RITONAVIR. RITONAVIR 1 Transplacental 1 DF, UNK 0 1 DF QD
125432371 12543237 3 SS EMTRICITABINE W/TENOFOVIR DISOPROXIL FUMARATE EMTRICITABINETENOFOVIR DISOPROXIL 1 Transplacental 1 DF, UNK 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125432371 12543237 1 Product used for unknown indication
125432371 12543237 2 Product used for unknown indication
125432371 12543237 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125432371 12543237 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125432371 12543237 Foetal exposure during pregnancy
125432371 12543237 Low birth weight baby

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
125432371 12543237 1 20151206 0
125432371 12543237 2 20151206 0
125432371 12543237 3 20151206 0