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
119250522 11925052 2 F 200009 20160826 20160118 20160826 EXP GB-BRISTOL-MYERS SQUIBB COMPANY-10765196 BRISTOL MYERS SQUIBB 1.00 DY M Y 0.00000 20160826 OT GB GB

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
119250522 11925052 1 PS VIDEX DIDANOSINE 1 Transplacental 400 MG, UNK Y 20156 400 MG
119250522 11925052 2 SS ZERIT STAVUDINE 1 Transplacental 80 MG, UNK Y 0 80 MG
119250522 11925052 3 SS NEVIRAPINE. NEVIRAPINE 1 Transplacental 400 MG, UNK Y 0 400 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119250522 11925052 1 Product used for unknown indication
119250522 11925052 2 Product used for unknown indication
119250522 11925052 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119250522 11925052 OT
119250522 11925052 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
119250522 11925052 Ependymoma
119250522 11925052 Foetal exposure during pregnancy
119250522 11925052 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
119250522 11925052 1 199812 20000927 0
119250522 11925052 2 199812 20000927 0
119250522 11925052 3 199911 20000927 0