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
118586292 11858629 2 F 20160824 20151222 20160824 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2007-000002 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160824 CN GB FR

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
118586292 11858629 1 PS SUSTIVA EFAVIRENZ 1 Transplacental 1 DF, UNK U 20972 1 DF CAPSULE
118586292 11858629 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 1 DF, UNK U 0 1 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118586292 11858629 1 Product used for unknown indication
118586292 11858629 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
118586292 11858629 OT
118586292 11858629 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
118586292 11858629 Foetal exposure during pregnancy
118586292 11858629 Heart disease congenital

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
118586292 11858629 1 20051201 20071211 0
118586292 11858629 2 20051201 0