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
121111444 12111144 4 F 20160705 20160224 20160718 EXP CH-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-004578 BRISTOL MYERS SQUIBB 0.00 N Y 0.00000 20160717 OT CH CH

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
121111444 12111144 1 PS ATAZANAVIR SULFATE ATAZANAVIR SULFATE 1 Transplacental UNK U 21567
121111444 12111144 2 SS PREZISTA DARUNAVIR ETHANOLATE 1 Transplacental UNK U 0
121111444 12111144 3 SS ISENTRESS RALTEGRAVIR POTASSIUM 1 Transplacental UNK U 0
121111444 12111144 4 SS COMBIVIR LAMIVUDINEIDOVUDINE 1 Transplacental UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121111444 12111144 1 Product used for unknown indication
121111444 12111144 2 Product used for unknown indication
121111444 12111144 3 Product used for unknown indication
121111444 12111144 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
121111444 12111144 CA
121111444 12111144 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121111444 12111144 Congenital cytomegalovirus infection
121111444 12111144 Congenital hepatomegaly
121111444 12111144 Dilatation ventricular
121111444 12111144 Electroencephalogram abnormal
121111444 12111144 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