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
118098922 11809892 2 F 20160826 20151208 20160826 EXP DE-BRISTOL-MYERS SQUIBB COMPANY-2001SUS0555 BRISTOL MYERS SQUIBB 27.00 YR F Y 0.00000 20160826 OT 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
118098922 11809892 1 PS SUSTIVA EFAVIRENZ 1 Oral UNK 20972
118098922 11809892 2 SS ZIDOVUDINE. ZIDOVUDINE 1 Unknown UNK UNK 0
118098922 11809892 3 SS LAMIVUDINE. LAMIVUDINE 1 Unknown UNK UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118098922 11809892 1 HIV infection
118098922 11809892 2 HIV infection
118098922 11809892 3 HIV infection

Outcome of event

Event ID CASEID OUTC COD
118098922 11809892 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118098922 11809892 Caesarean section
118098922 11809892 Live birth
118098922 11809892 Pregnancy
118098922 11809892 Premature rupture of membranes

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
118098922 11809892 2 19980501 0
118098922 11809892 3 19980501 0