The Safety Rates Drug Report

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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
125384772 12538477 2 F 20160614 20160708 20160707 20160719 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-053855 BRISTOL MYERS SQUIBB 36.00 YR F Y 0.00000 20160719 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
125384772 12538477 1 PS ATAZANAVIR SULFATE ATAZANAVIR SULFATE 1 Oral 300 MG, QD 21567 300 MG QD
125384772 12538477 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 1 DF, QD 0 1 DF QD
125384772 12538477 3 SS TIVICAY DOLUTEGRAVIR SODIUM 1 Oral 1 DF, QD Y 0 1 DF QD
125384772 12538477 4 SS NORVIR RITONAVIR 1 Oral 1 DF, QD 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125384772 12538477 1 HIV infection
125384772 12538477 2 HIV infection
125384772 12538477 3 HIV infection
125384772 12538477 4 HIV infection

Outcome of event

Event ID CASEID OUTC COD
125384772 12538477 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125384772 12538477 Abortion spontaneous
125384772 12538477 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
125384772 12538477 1 20160525 0
125384772 12538477 3 20160525 0
125384772 12538477 4 20160525 0