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
41808105 4180810 5 F 20160826 20040803 20160826 EXP GB-BRISTOL-MYERS SQUIBB COMPANY-12647988 BRISTOL MYERS SQUIBB 1.00 DY 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
41808105 4180810 1 PS VIDEX DIDANOSINE 1 Transplacental 250 MG, QD U 20156 250 MG QD
41808105 4180810 2 SS ZIDOVUDINE. ZIDOVUDINE 1 Transplacental 500 MG, QD U 0 500 MG QD
41808105 4180810 3 SS VIRAMUNE NEVIRAPINE 1 Transplacental 400 MG, QD U 0 400 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
41808105 4180810 1 Product used for unknown indication
41808105 4180810 2 Product used for unknown indication
41808105 4180810 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
41808105 4180810 CA
41808105 4180810 DE
41808105 4180810 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
41808105 4180810 Congenital anomaly
41808105 4180810 Foetal exposure during pregnancy

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

no results found

Therapies reported

no results found