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
73704554 7370455 4 F 20091130 20160819 20100429 20160826 EXP US-GILEAD-2010-0028688 GILEAD 40.00 YR A F Y 0.00000 20160826 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
73704554 7370455 1 PS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 21752 1 DF TABLET QD
73704554 7370455 2 SS EFAVIRENZ/EMTRICITABINE/TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZEMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral Y 0 1 DF QD
73704554 7370455 3 SS ATAZANAVIR ATAZANAVIR 1 Oral 300 MG, QD 0 300 MG QD
73704554 7370455 4 C RITONAVIR. RITONAVIR 1 Oral 100 MG, QD 0 100 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
73704554 7370455 1 HIV infection
73704554 7370455 2 HIV infection
73704554 7370455 3 HIV infection
73704554 7370455 4 HIV infection

Outcome of event

Event ID CASEID OUTC COD
73704554 7370455 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
73704554 7370455 Abortion induced
73704554 7370455 Amniocentesis abnormal
73704554 7370455 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
73704554 7370455 1 20091201 0
73704554 7370455 2 20091101 0
73704554 7370455 3 20091201 0
73704554 7370455 4 20091201 0