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
97053484 9705348 4 F 20160720 20131122 20160720 EXP IT-BRISTOL-MYERS SQUIBB COMPANY-19838705 BRISTOL MYERS SQUIBB 0.00 N Y 0.00000 20160720 OT 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
97053484 9705348 1 PS STAVUDINE. STAVUDINE 1 Transplacental UNK U 20412
97053484 9705348 2 SS LAMIVUDINE. LAMIVUDINE 1 Transplacental UNK U 0
97053484 9705348 3 SS NEVIRAPINE. NEVIRAPINE 1 Transplacental UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97053484 9705348 1 Product used for unknown indication
97053484 9705348 2 Product used for unknown indication
97053484 9705348 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
97053484 9705348 CA
97053484 9705348 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97053484 9705348 Cerebral ventricle dilatation
97053484 9705348 Congenital central nervous system anomaly
97053484 9705348 Congenital hydrocephalus
97053484 9705348 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