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
118849682 11884968 2 F 19980307 20160829 20160104 20160901 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-11678117 BRISTOL MYERS SQUIBB 0.00 DY M Y 2.95000 KG 20160901 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
118849682 11884968 1 PS ZERIT STAVUDINE 1 Transplacental UNK U 20412
118849682 11884968 2 SS VIDEX DIDANOSINE 1 Transplacental UNK U 0
118849682 11884968 3 SS RETROVIR ZIDOVUDINE 1 Transplacental UNK U 0
118849682 11884968 4 SS EPIVIR LAMIVUDINE 1 Oral UNK U 0
118849682 11884968 5 SS RETROVIR ZIDOVUDINE 1 Oral UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118849682 11884968 1 Product used for unknown indication
118849682 11884968 2 Product used for unknown indication
118849682 11884968 3 Product used for unknown indication
118849682 11884968 4 Antiretroviral therapy
118849682 11884968 5 Antiretroviral therapy

Outcome of event

Event ID CASEID OUTC COD
118849682 11884968 OT
118849682 11884968 CA
118849682 11884968 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
118849682 11884968 Albinism
118849682 11884968 Electroencephalogram abnormal
118849682 11884968 Foetal distress syndrome
118849682 11884968 Foetal exposure during pregnancy
118849682 11884968 Nystagmus
118849682 11884968 Urinary tract infection neonatal

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found