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
118157492 11815749 2 F 20021025 20160824 20151209 20160824 EXP US-BRISTOL-MYERS SQUIBB COMPANY-12155560 BRISTOL MYERS SQUIBB 27.00 YR F Y 0.00000 20160824 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
118157492 11815749 1 PS EFAVIRENZ EFAVIRENZ 1 Oral 600 MG, QD 40200 MG 20972 600 MG QD
118157492 11815749 2 SS VIDEX DIDANOSINE 1 Oral 400 MG, QD 37200 MG 0 400 MG POWDER FOR ORAL SOLUTION QD
118157492 11815749 3 C EPIVIR LAMIVUDINE 1 Oral 300 MG, QD 0 300 MG QD
118157492 11815749 4 C KALETRA LOPINAVIRRITONAVIR 1 Oral 200/800MG 0
118157492 11815749 5 C TRIZIVIR ABACAVIR SULFATELAMIVUDINEIDOVUDINE 1 Oral 600/600/300 MG 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118157492 11815749 1 HIV infection
118157492 11815749 2 HIV infection
118157492 11815749 3 HIV infection
118157492 11815749 4 HIV infection
118157492 11815749 5 HIV infection

Outcome of event

Event ID CASEID OUTC COD
118157492 11815749 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118157492 11815749 Live birth
118157492 11815749 Premature delivery
118157492 11815749 Twin pregnancy

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
118157492 11815749 1 20020318 20020523 0
118157492 11815749 2 20020725 20021025 0
118157492 11815749 3 20020318 20021025 0
118157492 11815749 4 20020725 20021025 0
118157492 11815749 5 20020318 20020523 0