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
60548203 6054820 3 F 20050409 20160822 20060530 20160822 EXP DE-BRISTOL-MYERS SQUIBB COMPANY-13373154 BRISTOL MYERS SQUIBB 0.00 DY F Y 0.00000 20160822 MD DE DE

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
60548203 6054820 1 PS REYATAZ ATAZANAVIR SULFATE 1 Transplacental 400 MG, QD U 21567 400 MG QD
60548203 6054820 2 SS VIDEX EC DIDANOSINE 1 Transplacental 250 MG, QD U 0 250 MG GASTRO-RESISTANT CAPSULE, HARD QD
60548203 6054820 3 SS VIREAD TENOFOVIR DISOPROXIL FUMARATE 1 Transplacental 300 MG, QD U 0 300 MG QD
60548203 6054820 4 SS VIRAMUNE NEVIRAPINE 1 Transplacental 400 MG, QD U 0 400 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
60548203 6054820 1 Product used for unknown indication
60548203 6054820 2 Product used for unknown indication
60548203 6054820 3 Product used for unknown indication
60548203 6054820 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
60548203 6054820 HO
60548203 6054820 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
60548203 6054820 Foetal exposure during pregnancy
60548203 6054820 Premature baby

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
60548203 6054820 1 20050409 0
60548203 6054820 2 20050409 0
60548203 6054820 3 20050409 0
60548203 6054820 4 20050409 0