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
69083844 6908384 4 F 20081119 20160822 20090212 20160822 EXP GB-BRISTOL-MYERS SQUIBB COMPANY-14218549 BRISTOL MYERS SQUIBB 39.03 YR F Y 0.00000 20160822 MD GB GB

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
69083844 6908384 1 PS REYATAZ ATAZANAVIR SULFATE 1 Oral 300 MG, QD 21567 300 MG CAPSULE, HARD QD
69083844 6908384 2 SS DIDANOSINE. DIDANOSINE 1 Oral 200 MG, QD 438000 MG Y 0 200 MG POWDER FOR ORAL SOLUTION QD
69083844 6908384 3 SS VIREAD TENOFOVIR DISOPROXIL FUMARATE 1 Oral 245 MG, QD U 0 245 MG QD
69083844 6908384 4 SS RITONAVIR. RITONAVIR 1 Oral 100 MG, QD 0 100 MG QD
69083844 6908384 5 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 1 DF, QD 1 DF Y 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
69083844 6908384 1 HIV infection
69083844 6908384 2 HIV infection
69083844 6908384 3 HIV infection
69083844 6908384 4 HIV infection
69083844 6908384 5 HIV infection

Outcome of event

Event ID CASEID OUTC COD
69083844 6908384 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
69083844 6908384 Caesarean section
69083844 6908384 Live birth
69083844 6908384 Maternal exposure during 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
69083844 6908384 1 2002 0
69083844 6908384 2 2002 20080630 0
69083844 6908384 3 2002 0
69083844 6908384 4 2002 0
69083844 6908384 5 20080630 20080630 0