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
127182991 12718299 1 I 20140624 20160906 20160906 EXP IT-GILEAD-2014-0106943 GILEAD 0.00 I M Y 2.52000 KG 20160906 OT IT IT

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
127182991 12718299 1 PS EMTRIVA EMTRICITABINE 1 Transplacental UNK U 21500 CAPSULE
127182991 12718299 2 SS VIREAD TENOFOVIR DISOPROXIL FUMARATE 1 Transplacental U 0 TABLET
127182991 12718299 3 SS REYATAZ ATAZANAVIR SULFATE 1 Transplacental UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127182991 12718299 1 Prophylaxis against HIV infection
127182991 12718299 2 Prophylaxis against HIV infection
127182991 12718299 3 Prophylaxis against HIV infection

Outcome of event

Event ID CASEID OUTC COD
127182991 12718299 CA
127182991 12718299 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127182991 12718299 Cryptorchism
127182991 12718299 Foetal 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
127182991 12718299 1 2009 0
127182991 12718299 3 2009 0