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
41627246 4162724 6 F 20160826 20040701 20160826 EXP GB-BRISTOL-MYERS SQUIBB COMPANY-12621512 BRISTOL MYERS SQUIBB 0.00 Y 0.00000 20160826 OT GB GB

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
41627246 4162724 1 PS VIDEX DIDANOSINE 1 Transplacental 400 MG, QD U 20156 400 MG QD
41627246 4162724 2 SS NEVIRAPINE. NEVIRAPINE 1 Transplacental 400 MG, QD U 0 400 MG QD
41627246 4162724 3 SS RETROVIR ZIDOVUDINE 1 Transplacental 500 MG, QD U 0 500 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
41627246 4162724 1 Product used for unknown indication
41627246 4162724 2 Product used for unknown indication
41627246 4162724 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
41627246 4162724 CA
41627246 4162724 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
41627246 4162724 Brain malformation
41627246 4162724 Congenital central nervous system anomaly
41627246 4162724 Foetal exposure during pregnancy
41627246 4162724 Pulmonary hypoplasia

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
41627246 4162724 1 20040122 0
41627246 4162724 2 20000122 0
41627246 4162724 3 200001 0