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
97566543 9756654 3 F 20160722 20131213 20160722 EXP ET-BRISTOL-MYERS SQUIBB COMPANY-19886787 BRISTOL MYERS SQUIBB 0.00 Y 0.00000 20160722 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
97566543 9756654 1 PS EFAVIRENZ EFAVIRENZ 1 Transplacental UNK U 20972
97566543 9756654 2 SS ZIDOVUDINE. ZIDOVUDINE 1 Transplacental UNK U 0
97566543 9756654 3 SS LAMIVUDINE. LAMIVUDINE 1 Transplacental UNK U 0
97566543 9756654 4 SS NEVIRAPINE. NEVIRAPINE 1 Transplacental UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97566543 9756654 1 Product used for unknown indication
97566543 9756654 2 Product used for unknown indication
97566543 9756654 3 Product used for unknown indication
97566543 9756654 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
97566543 9756654 OT
97566543 9756654 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
97566543 9756654 Encephalocele
97566543 9756654 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