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
127676692 12767669 2 F 20160919 20160921 20160926 EXP MZ-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-075444 BRISTOL MYERS SQUIBB 0.00 N F Y 1.48000 KG 20160926 OT MZ MZ

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
127676692 12767669 1 PS EFAVIRENZ EFAVIRENZ 1 Transplacental 600 MG, UNK U 20972 600 MG
127676692 12767669 2 SS TENOFOVIR TENOFOVIR 1 Transplacental 300 MG, UNK U 0 300 MG
127676692 12767669 3 SS LAMIVUDINE. LAMIVUDINE 1 Transplacental 300 MG, UNK U 0 300 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127676692 12767669 1 Product used for unknown indication
127676692 12767669 2 Product used for unknown indication
127676692 12767669 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127676692 12767669 HO
127676692 12767669 DE
127676692 12767669 CA
127676692 12767669 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127676692 12767669 Aplasia cutis congenita
127676692 12767669 Fistula
127676692 12767669 Foetal exposure during pregnancy
127676692 12767669 Low birth weight baby

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

no results found

Therapies reported

no results found