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
73705944 7370594 4 F 20100311 20160822 20100429 20160825 EXP US-GILEAD-2010-0028690 GILEAD 0.00 Y 0.00000 20160825 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
73705944 7370594 1 PS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental UNK 21752 TABLET
73705944 7370594 2 SS EFAVIRENZ/EMTRICITABINE/TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZEMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental 0 TABLET
73705944 7370594 3 SS ATAZANAVIR ATAZANAVIR 1 Transplacental 300 MG, QD 30000 MG 0 300 MG QD
73705944 7370594 4 SS RITONAVIR. RITONAVIR 1 Transplacental UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
73705944 7370594 1 HIV infection
73705944 7370594 2 HIV infection
73705944 7370594 3 HIV infection
73705944 7370594 4 HIV infection

Outcome of event

Event ID CASEID OUTC COD
73705944 7370594 OT
73705944 7370594 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
73705944 7370594 Foetal exposure during pregnancy
73705944 7370594 Klinefelter's syndrome

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
73705944 7370594 1 20091201 20100327 0
73705944 7370594 2 20091101 0
73705944 7370594 3 20091201 20100327 0
73705944 7370594 4 20091201 20100327 0