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
122889673 12288967 3 F 20160809 20160421 20160809 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-027945 BRISTOL MYERS SQUIBB 0.00 N Y 0.00000 20160809 CN 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
122889673 12288967 1 PS ATAZANAVIR SULFATE ATAZANAVIR SULFATE 1 Transplacental UNK U 21567
122889673 12288967 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental UNK U 0
122889673 12288967 3 SS ISENTRESS RALTEGRAVIR POTASSIUM 1 Transplacental UNK U 0
122889673 12288967 4 SS NORVIR RITONAVIR 1 Transplacental UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122889673 12288967 1 Product used for unknown indication
122889673 12288967 2 Product used for unknown indication
122889673 12288967 3 Product used for unknown indication
122889673 12288967 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
122889673 12288967 OT
122889673 12288967 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
122889673 12288967 Foetal exposure during pregnancy
122889673 12288967 Heart disease congenital

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

no results found

Therapies reported

no results found