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
73265815 7326581 5 F 20160908 20100321 20160909 EXP US-BRISTOL-MYERS SQUIBB COMPANY-15024797 BRISTOL MYERS SQUIBB 0.00 Y 0.00000 20160909 OT US US

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
73265815 7326581 1 PS SUSTIVA EFAVIRENZ 1 Transplacental UNK U 20972 CAPSULE
73265815 7326581 2 SS TENOFOVIR DISOPROXIL FUMARATE. TENOFOVIR DISOPROXIL FUMARATE 1 Transplacental UNK U 0
73265815 7326581 3 SS EMTRICITABINE EMTRICITABINE 1 Transplacental UNK U 0
73265815 7326581 4 SS ABACAVIR. ABACAVIR 1 Transplacental UNK U 0
73265815 7326581 5 SS LAMIVUDINE. LAMIVUDINE 1 Transplacental UNK U 0
73265815 7326581 6 SS ZIDOVUDINE. ZIDOVUDINE 1 Transplacental UNK U 0
73265815 7326581 7 SS NELFINAVIR NELFINAVIR 1 Transplacental UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
73265815 7326581 1 Product used for unknown indication
73265815 7326581 2 Product used for unknown indication
73265815 7326581 3 Product used for unknown indication
73265815 7326581 4 Product used for unknown indication
73265815 7326581 5 Product used for unknown indication
73265815 7326581 6 Product used for unknown indication
73265815 7326581 7 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
73265815 7326581 OT
73265815 7326581 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
73265815 7326581 Foetal exposure during pregnancy
73265815 7326581 Gastroschisis

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

no results found

Therapies reported

no results found