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
57695837 5769583 7 F 20040831 20160825 20050404 20160825 EXP US-BRISTOL-MYERS SQUIBB COMPANY-12845400 BRISTOL MYERS SQUIBB 1.00 DY M Y 1.73000 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
57695837 5769583 1 PS STAVUDINE. STAVUDINE 1 Transplacental 40 MG, Q12H U 20412 40 MG BID
57695837 5769583 2 SS EPIVIR LAMIVUDINE 1 Transplacental 150 MG, Q12H U 0 150 MG BID
57695837 5769583 3 SS KALETRA LOPINAVIRRITONAVIR 1 Transplacental 1 DF, Q12H U 0 1 DF BID
57695837 5769583 4 SS SPORANOX ITRACONAZOLE 1 Transplacental UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
57695837 5769583 1 Product used for unknown indication
57695837 5769583 2 Product used for unknown indication
57695837 5769583 3 Product used for unknown indication
57695837 5769583 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
57695837 5769583 CA
57695837 5769583 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
57695837 5769583 Brain malformation
57695837 5769583 Breech presentation
57695837 5769583 Congenital central nervous system anomaly
57695837 5769583 Congenital genital malformation
57695837 5769583 Foetal exposure during pregnancy
57695837 5769583 Low birth weight baby
57695837 5769583 Microcephaly
57695837 5769583 Umbilical cord vascular disorder

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found