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
97053604 9705360 4 F 20160822 20131122 20160824 EXP IT-BRISTOL-MYERS SQUIBB COMPANY-19838580 BRISTOL MYERS SQUIBB 0.00 Y 0.00000 20160824 CN IT IT

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
97053604 9705360 1 PS ATAZANAVIR SULFATE ATAZANAVIR SULFATE 1 Transplacental UNK U 21567
97053604 9705360 2 SS LAMIVUDINE. LAMIVUDINE 1 Transplacental UNK U 0
97053604 9705360 3 SS TENOFOVIR TENOFOVIR 1 Transplacental UNK U 0
97053604 9705360 4 SS RITONAVIR. RITONAVIR 1 Transplacental U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97053604 9705360 1 Product used for unknown indication
97053604 9705360 2 Product used for unknown indication
97053604 9705360 3 Product used for unknown indication
97053604 9705360 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
97053604 9705360 OT
97053604 9705360 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
97053604 9705360 Foetal exposure during pregnancy
97053604 9705360 Trisomy 18

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

no results found

Therapies reported

no results found