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
67976027 6797602 7 F 20070611 20160822 20081028 20160822 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-14332951 BRISTOL MYERS SQUIBB 34.72 YR F Y 92.00000 KG 20160822 MD FR FR

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
67976027 6797602 1 PS REYATAZ ATAZANAVIR SULFATE 1 Oral 300 MG, QD 34500 MG 21567 300 MG CAPSULE, HARD QD
67976027 6797602 2 SS SUSTIVA EFAVIRENZ 1 Oral 600 MG, QD 0 600 MG CAPSULE QD
67976027 6797602 3 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 1 DF, QD 0 1 DF QD
67976027 6797602 4 SS NORVIR RITONAVIR 1 Oral PTC TO DELIVERY 0 100 MG QD
67976027 6797602 5 SS KALETRA LOPINAVIRRITONAVIR 1 Oral UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
67976027 6797602 1 HIV infection
67976027 6797602 2 HIV infection
67976027 6797602 3 HIV infection
67976027 6797602 4 HIV infection
67976027 6797602 5 HIV infection

Outcome of event

Event ID CASEID OUTC COD
67976027 6797602 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
67976027 6797602 Abortion induced
67976027 6797602 Oligohydramnios
67976027 6797602 Pregnancy on contraceptive

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
67976027 6797602 1 20070217 20070703 0
67976027 6797602 2 20060914 20070217 0
67976027 6797602 3 20060914 0
67976027 6797602 4 20070217 20070703 0