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
119005702 11900570 2 F 200308 20160825 20160108 20160825 EXP US-BRISTOL-MYERS SQUIBB COMPANY-12409793 BRISTOL MYERS SQUIBB 44.00 YR F Y 0.00000 20160825 OT US US

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
119005702 11900570 1 PS STAVUDINE. STAVUDINE 1 Oral 80 MG, QD 20412 80 MG QD
119005702 11900570 2 SS EPIVIR LAMIVUDINE 1 Oral 300 MG, QD 0 300 MG QD
119005702 11900570 3 SS CRIXIVAN INDINAVIR SULFATE 1 Oral 1600 MG, QD 0 1600 MG QD
119005702 11900570 4 SS NORVIR RITONAVIR 1 Oral 200 MG, QD 0 200 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119005702 11900570 1 HIV infection
119005702 11900570 2 HIV infection
119005702 11900570 3 HIV infection
119005702 11900570 4 HIV infection

Outcome of event

Event ID CASEID OUTC COD
119005702 11900570 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119005702 11900570 Pregnancy
119005702 11900570 Premature delivery
119005702 11900570 Premature rupture of membranes
119005702 11900570 Premature separation of placenta

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
119005702 11900570 1 19991210 0
119005702 11900570 2 19991210 0
119005702 11900570 3 19991210 0
119005702 11900570 4 19991210 0