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
62104403 6210440 3 F 19980407 20160826 20070108 20160827 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-13633565 BRISTOL MYERS SQUIBB 0.00 DY F Y 0.00000 20160827 OT FR FR

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
62104403 6210440 1 PS ZERIT STAVUDINE 1 Transplacental UNK U 20412
62104403 6210440 2 SS EPIVIR LAMIVUDINE 1 Transplacental UNK U 0
62104403 6210440 3 SS RIFADINE RIFAMPIN 1 Transplacental UNK U 0
62104403 6210440 4 SS RIMIFON ISONIAZID 1 Transplacental UNK U 0
62104403 6210440 5 SS RETROVIR ZIDOVUDINE 1 Unknown UNK U 0
62104403 6210440 6 SS EPIVIR LAMIVUDINE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
62104403 6210440 1 Product used for unknown indication
62104403 6210440 2 Product used for unknown indication
62104403 6210440 3 Product used for unknown indication
62104403 6210440 4 Product used for unknown indication
62104403 6210440 5 Product used for unknown indication
62104403 6210440 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
62104403 6210440 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
62104403 6210440 Cardiac murmur
62104403 6210440 Foetal distress syndrome
62104403 6210440 Foetal exposure during pregnancy

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
62104403 6210440 5 19980408 0
62104403 6210440 6 19980408 0