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
118812502 11881250 2 F 20020315 20160906 20151231 20160906 EXP US-BRISTOL-MYERS SQUIBB COMPANY-11831146 BRISTOL MYERS SQUIBB 0.00 Y 0.00000 20160906 MD 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
118812502 11881250 1 PS STAVUDINE. STAVUDINE 1 Transplacental 80 MG, QD U 20412 80 MG QD
118812502 11881250 2 SS EPIVIR LAMIVUDINE 1 Transplacental 300 MG, QD U 0 300 MG QD
118812502 11881250 3 SS VIRACEPT NELFINAVIR MESYLATE 1 Transplacental 2500 MG, QD U 0 2500 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118812502 11881250 1 Product used for unknown indication
118812502 11881250 2 Product used for unknown indication
118812502 11881250 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
118812502 11881250 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
118812502 11881250 Congenital anomaly
118812502 11881250 Foetal exposure during pregnancy

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
118812502 11881250 1 20020131 0
118812502 11881250 2 20020131 0
118812502 11881250 3 20020131 0