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
102887253 10288725 3 F 20160822 20140709 20160824 EXP IT-BRISTOL-MYERS SQUIBB COMPANY-21183926 BRISTOL MYERS SQUIBB 0.00 N M Y 2.52000 KG 20160824 CN IT IT

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
102887253 10288725 1 PS ATAZANAVIR SULFATE ATAZANAVIR SULFATE 1 Transplacental UNK U 21567
102887253 10288725 2 SS EMTRICITABINE EMTRICITABINE 1 Transplacental UNK U 0
102887253 10288725 3 SS TENOFOVIR TENOFOVIR 1 Transplacental UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
102887253 10288725 1 Product used for unknown indication
102887253 10288725 2 Product used for unknown indication
102887253 10288725 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
102887253 10288725 OT
102887253 10288725 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
102887253 10288725 Cryptorchism
102887253 10288725 Foetal exposure during pregnancy

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
102887253 10288725 1 2009 0
102887253 10288725 2 2009 0
102887253 10288725 3 2009 0