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
117392932 11739293 2 F 2008 20160824 20151113 20160824 EXP ZA-BRISTOL-MYERS SQUIBB COMPANY-14652952 BRISTOL MYERS SQUIBB 36.00 YR F Y 0.00000 20160824 OT ZA ZA

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
117392932 11739293 1 PS EFAVIRENZ EFAVIRENZ 1 Oral 600 MG, QD 20972 600 MG QD
117392932 11739293 2 C COMBIVIR LAMIVUDINEIDOVUDINE 1 Unknown UNK 0
117392932 11739293 3 C VIRAMUNE NEVIRAPINE 1 Oral 400 MG, QD 0 400 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117392932 11739293 1 HIV infection
117392932 11739293 2 HIV infection
117392932 11739293 3 HIV infection

Outcome of event

Event ID CASEID OUTC COD
117392932 11739293 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117392932 11739293 Caesarean section
117392932 11739293 Maternal exposure during pregnancy
117392932 11739293 Stillbirth

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
117392932 11739293 1 20060201 0
117392932 11739293 2 20060201 0
117392932 11739293 3 20081009 0