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
57201293 5720129 3 F 20040730 20160826 20050121 20160826 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-12821740 BRISTOL MYERS SQUIBB 0.00 DY M Y 1.50000 KG 20160826 CN 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
57201293 5720129 1 PS VIDEX DIDANOSINE 1 Transplacental UNK U 20156
57201293 5720129 2 SS EPIVIR LAMIVUDINE 1 Transplacental UNK U 0
57201293 5720129 3 SS VIRACEPT NELFINAVIR MESYLATE 1 Transplacental UNK U 0
57201293 5720129 4 C ZIDOVUDINE. ZIDOVUDINE 1 Intravenous (not otherwise specified) 1.5 MG/KG, BID U 0 1.5 MG/KG BID
57201293 5720129 5 C ZIDOVUDINE. ZIDOVUDINE 1 Oral UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
57201293 5720129 1 Product used for unknown indication
57201293 5720129 2 Product used for unknown indication
57201293 5720129 3 Product used for unknown indication
57201293 5720129 4 Product used for unknown indication
57201293 5720129 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
57201293 5720129 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
57201293 5720129 Abdominal distension
57201293 5720129 Foetal exposure during pregnancy
57201293 5720129 Meconium stain
57201293 5720129 Premature baby
57201293 5720129 Selective eating disorder

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
57201293 5720129 2 20040730 0
57201293 5720129 3 20040730 0
57201293 5720129 4 20040730 2004 0
57201293 5720129 5 2004 0