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
119152632 11915263 2 F 20010402 20160825 20160114 20160825 EXP DE-BRISTOL-MYERS SQUIBB COMPANY-11544822 BRISTOL MYERS SQUIBB 0.00 DY M Y 1.75000 KG 20160825 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
119152632 11915263 1 PS VIDEX DIDANOSINE 1 Transplacental 325 MG, QD U 20156 325 MG QD
119152632 11915263 2 SS STAVUDINE. STAVUDINE 1 Transplacental 60 MG, QD U 0 60 MG QD
119152632 11915263 3 SS VIRAMUNE NEVIRAPINE 1 Transplacental 400 MG, QD U 0 400 MG QD
119152632 11915263 4 SS RETROVIR ZIDOVUDINE 1 Transplacental 100 MG, QD U 0 100 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119152632 11915263 1 Product used for unknown indication
119152632 11915263 2 Product used for unknown indication
119152632 11915263 3 Product used for unknown indication
119152632 11915263 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119152632 11915263 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119152632 11915263 Apnoea
119152632 11915263 Foetal exposure during pregnancy
119152632 11915263 Hypocalcaemia
119152632 11915263 Hypoglycaemia
119152632 11915263 Premature baby
119152632 11915263 Pulmonary oedema

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
119152632 11915263 1 20010401 0
119152632 11915263 2 20010401 0
119152632 11915263 3 20010401 0
119152632 11915263 4 20010402 20010402 0