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
60135523 6013552 3 F 200206 20160824 20060328 20160824 EXP DE-BRISTOL-MYERS SQUIBB COMPANY-13322532 BRISTOL MYERS SQUIBB 0.00 M Y 2.60000 KG 20160824 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
60135523 6013552 1 PS SUSTIVA EFAVIRENZ 1 Transplacental UNK U 20972
60135523 6013552 2 C ZIDOVUDINE. ZIDOVUDINE 1 Transplacental UNK U 0
60135523 6013552 3 C LAMIVUDINE. LAMIVUDINE 1 Transplacental UNK U 0
60135523 6013552 4 C NEVIRAPINE. NEVIRAPINE 1 Transplacental UNK U 0
60135523 6013552 5 C ACTRAPHANE INSULIN HUMAN 1 Transplacental UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
60135523 6013552 1 Product used for unknown indication
60135523 6013552 2 Product used for unknown indication
60135523 6013552 3 Product used for unknown indication
60135523 6013552 4 Product used for unknown indication
60135523 6013552 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
60135523 6013552 OT
60135523 6013552 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
60135523 6013552 Dyspnoea
60135523 6013552 Foetal exposure during pregnancy
60135523 6013552 Group B streptococcus neonatal sepsis
60135523 6013552 Rotavirus infection

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
60135523 6013552 1 200110 0
60135523 6013552 2 200110 0
60135523 6013552 3 200110 0
60135523 6013552 4 200110 200206 0