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
125855561 12585556 1 I 20150731 20160725 20160725 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-094004 BRISTOL MYERS SQUIBB 0.00 M Y 0.67000 KG 20160725 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
125855561 12585556 1 PS ATAZANAVIR SULFATE ATAZANAVIR SULFATE 1 Transplacental 1 DF, QD 21567 1 DF QD
125855561 12585556 2 SS RITONAVIR. RITONAVIR 1 Transplacental 1 DF, QD 0 1 DF QD
125855561 12585556 3 SS EMTRICITABINE / TENOFOVIR DISOPROXIL FUMARATE EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental 1 DF, QD 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125855561 12585556 1 Product used for unknown indication
125855561 12585556 2 Product used for unknown indication
125855561 12585556 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125855561 12585556 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125855561 12585556 Foetal exposure during pregnancy
125855561 12585556 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
125855561 12585556 1 20130508 0
125855561 12585556 2 20130508 0
125855561 12585556 3 20130508 0