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
65207925 6520792 5 F 2007 20160822 20080107 20160822 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-14029631 BRISTOL MYERS SQUIBB 0.00 M Y 2.20000 KG 20160822 MD FR FR

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
65207925 6520792 1 PS REYATAZ ATAZANAVIR SULFATE 1 Transplacental UNK 21567 CAPSULE, HARD
65207925 6520792 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental UNK U 0
65207925 6520792 3 SS NORVIR RITONAVIR 1 Transplacental UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
65207925 6520792 1 Product used for unknown indication
65207925 6520792 2 Product used for unknown indication
65207925 6520792 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
65207925 6520792 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
65207925 6520792 Atrophy
65207925 6520792 Breech presentation
65207925 6520792 Foetal exposure during pregnancy
65207925 6520792 Foetal growth restriction

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
65207925 6520792 1 20071012 0
65207925 6520792 2 20071012 0
65207925 6520792 3 20071012 0