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
119143802 11914380 2 F 20030824 20160825 20160113 20160825 EXP US-BRISTOL-MYERS SQUIBB COMPANY-12416343 BRISTOL MYERS SQUIBB 0.00 DY F Y 0.52000 KG 20160825 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
119143802 11914380 1 PS STAVUDINE. STAVUDINE 1 Transplacental 80 MG, QD U 20412 80 MG QD
119143802 11914380 2 SS EPIVIR LAMIVUDINE 1 Transplacental 300 MG, QD U 0 300 MG QD
119143802 11914380 3 SS CRIXIVAN INDINAVIR SULFATE 1 Transplacental EXPOSURE BEGAN AT CONCEPTION. U 0 1600 MG QD
119143802 11914380 4 SS NORVIR RITONAVIR 1 Transplacental 200 MG, QD U 0 200 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119143802 11914380 1 Product used for unknown indication
119143802 11914380 2 Product used for unknown indication
119143802 11914380 3 Product used for unknown indication
119143802 11914380 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119143802 11914380 OT
119143802 11914380 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
119143802 11914380 Death neonatal
119143802 11914380 Foetal exposure during pregnancy
119143802 11914380 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
119143802 11914380 3 20030824 0
119143802 11914380 4 20030824 0