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
119141462 11914146 2 F 200009 20160826 20160113 20160826 EXP GB-BRISTOL-MYERS SQUIBB COMPANY-10702587 BRISTOL MYERS SQUIBB 34.62 YR F Y 68.00000 KG 20160826 OT GB GB

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
119141462 11914146 1 PS ZERIT STAVUDINE 1 Oral 80 MG, QD Y 20412 80 MG QD
119141462 11914146 2 SS VIDEX DIDANOSINE 1 Oral 400 MG, QD Y 0 400 MG QD
119141462 11914146 3 SS NEVIRAPINE. NEVIRAPINE 1 Oral 400 MG, QD Y 0 400 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119141462 11914146 1 HIV infection
119141462 11914146 2 HIV infection
119141462 11914146 3 HIV infection

Outcome of event

Event ID CASEID OUTC COD
119141462 11914146 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119141462 11914146 Caesarean section
119141462 11914146 Hepatitis
119141462 11914146 Lactic acidosis
119141462 11914146 Lipodystrophy acquired
119141462 11914146 Meconium stain
119141462 11914146 Neuropathy peripheral
119141462 11914146 Oedema
119141462 11914146 Pre-eclampsia
119141462 11914146 Pregnancy
119141462 11914146 Premature delivery

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
119141462 11914146 1 199812 20000927 0
119141462 11914146 2 199812 20000927 0
119141462 11914146 3 199911 20000927 0