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
635651610 6356516 10 F 20070702 20160824 20070713 20160825 EXP US-BRISTOL-MYERS SQUIBB COMPANY-13837919 BRISTOL MYERS SQUIBB 0.00 YR F Y 1.11000 KG 20160825 CN 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
635651610 6356516 1 PS EFAVIRENZ EFAVIRENZ 1 Transplacental 1 DF, UNK Y 20972 1 DF
635651610 6356516 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental 1 DF, QD U 0 1 DF QD
635651610 6356516 3 SS VIRAMUNE NEVIRAPINE 1 Transplacental 1 DF, QD U 0 1 DF QD
635651610 6356516 4 C BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Transplacental UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
635651610 6356516 1 Product used for unknown indication
635651610 6356516 2 Product used for unknown indication
635651610 6356516 3 Product used for unknown indication
635651610 6356516 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
635651610 6356516 OT
635651610 6356516 CA
635651610 6356516 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
635651610 6356516 Breech presentation
635651610 6356516 Dandy-Walker syndrome
635651610 6356516 Foetal exposure during pregnancy
635651610 6356516 Foetal growth restriction
635651610 6356516 Foetal malformation
635651610 6356516 Umbilical cord around neck

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
635651610 6356516 1 20070201 0
635651610 6356516 2 20070201 0
635651610 6356516 3 20070201 0