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
63018154 6301815 4 F 20021106 20160826 20070501 20160827 EXP JP-BRISTOL-MYERS SQUIBB COMPANY-13392873 BRISTOL MYERS SQUIBB 29.02 YR F Y 0.00000 20160827 CN JP JP

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
63018154 6301815 1 PS ZERIT STAVUDINE 1 Oral 60 MG, QD 20412 60 MG QD
63018154 6301815 2 SS EPIVIR LAMIVUDINE 1 Oral 300 MG, QD 0 300 MG QD
63018154 6301815 3 SS VIRACEPT NELFINAVIR MESYLATE 1 Oral 2500 MG, QD 0 2500 MG QD
63018154 6301815 4 C RETROVIR ZIDOVUDINE 1 Intravenous (not otherwise specified) UNK Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
63018154 6301815 1 HIV infection
63018154 6301815 2 HIV infection
63018154 6301815 3 HIV infection
63018154 6301815 4 Prophylaxis against HIV infection

Outcome of event

Event ID CASEID OUTC COD
63018154 6301815 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
63018154 6301815 Anaemia
63018154 6301815 Blood triglycerides increased
63018154 6301815 Caesarean section
63018154 6301815 Deep vein thrombosis
63018154 6301815 Live birth
63018154 6301815 Musculoskeletal pain
63018154 6301815 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
63018154 6301815 1 19990203 0
63018154 6301815 2 19990203 0
63018154 6301815 3 19990210 0
63018154 6301815 4 20050728 20050728 0