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
108013893 10801389 3 F 20140929 20160728 20150217 20160801 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-008318 BRISTOL MYERS SQUIBB 31.00 YR F Y 0.00000 20160801 OT BR BR

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
108013893 10801389 1 PS ATAZANAVIR SULFATE ATAZANAVIR SULFATE 1 Oral 300 MG, QD 21567 300 MG QD
108013893 10801389 2 SS NORVIR RITONAVIR 1 Oral 100 MG, QD 0 100 MG QD
108013893 10801389 3 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 500 MG, QD 0 500 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
108013893 10801389 1 HIV infection
108013893 10801389 2 HIV infection
108013893 10801389 3 HIV infection

Outcome of event

Event ID CASEID OUTC COD
108013893 10801389 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
108013893 10801389 Abortion spontaneous
108013893 10801389 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
108013893 10801389 1 20130318 0
108013893 10801389 2 20130318 0
108013893 10801389 3 20130318 0