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
118093802 11809380 2 F 20160726 20151207 20160726 EXP ET-BRISTOL-MYERS SQUIBB COMPANY-19912997 BRISTOL MYERS SQUIBB 35.00 YR F Y 0.00000 20160726 OT ET ET

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
118093802 11809380 1 PS EFAVIRENZ EFAVIRENZ 1 Unknown UNK Y 20972
118093802 11809380 2 C ZIDOVUDINE. ZIDOVUDINE 1 Unknown UNK U 0
118093802 11809380 3 C LAMIVUDINE. LAMIVUDINE 1 Unknown UNK U 0
118093802 11809380 4 C NEVIRAPINE. NEVIRAPINE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118093802 11809380 1 HIV infection
118093802 11809380 2 HIV infection
118093802 11809380 3 HIV infection
118093802 11809380 4 HIV infection

Outcome of event

Event ID CASEID OUTC COD
118093802 11809380 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118093802 11809380 Induced labour
118093802 11809380 Maternal exposure during pregnancy
118093802 11809380 Stillbirth

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

no results found

Therapies reported

no results found