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
117837662 11783766 2 F 20071207 20160819 20151127 20160819 EXP PR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2007-000010 BRISTOL MYERS SQUIBB 0.00 DY M Y 2.13000 KG 20160819 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
117837662 11783766 1 PS ATAZANAVIR SULFATE ATAZANAVIR SULFATE 1 Transplacental 300 MG, QD U 21567 300 MG CAPSULE, HARD QD
117837662 11783766 2 SS ATAZANAVIR SULFATE ATAZANAVIR SULFATE 1 Transplacental 400 MG, QD U 21567 400 MG CAPSULE, HARD QD
117837662 11783766 3 SS RITONAVIR. RITONAVIR 1 Transplacental 100 MG, QD U 0 100 MG QD
117837662 11783766 4 SS LAMIVUDINE,ZIDOVUDINE LAMIVUDINEIDOVUDINE 1 Transplacental UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117837662 11783766 1 Product used for unknown indication
117837662 11783766 3 Product used for unknown indication
117837662 11783766 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
117837662 11783766 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117837662 11783766 Foetal exposure during pregnancy
117837662 11783766 Foetal growth restriction
117837662 11783766 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
117837662 11783766 1 20070720 20071107 0
117837662 11783766 2 20071107 0
117837662 11783766 3 20070720 0
117837662 11783766 4 20070720 0