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
125241322 12524132 2 F 20150621 20160701 20160704 20160712 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-052164 BRISTOL MYERS SQUIBB 0.00 DY M Y 1.19000 KG 20160712 OT US US

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
125241322 12524132 1 PS ATAZANAVIR SULFATE ATAZANAVIR SULFATE 1 Transplacental 400 MG, QD 46800 MG 21567 400 MG QD
125241322 12524132 2 SS NORVIR RITONAVIR 1 Transplacental 100 MG, QD 11700 MG 0 100 MG QD
125241322 12524132 3 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental 1 DF, QD 117 DF 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125241322 12524132 1 Product used for unknown indication
125241322 12524132 2 Product used for unknown indication
125241322 12524132 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125241322 12524132 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125241322 12524132 Foetal exposure during pregnancy
125241322 12524132 Premature 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
125241322 12524132 1 20150225 20150621 0
125241322 12524132 2 20150225 20150621 0
125241322 12524132 3 20150225 20150621 0