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
87843444 8784344 4 F 20160831 20120913 20160902 EXP GB-GILEAD-2012-0060487 GILEAD 0.00 F Y 0.00000 20160902 CN GB GB

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
87843444 8784344 1 PS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental UNK UNK, QD U U 21752 1 DF TABLET QD
87843444 8784344 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 U U 21752 TABLET
87843444 8784344 3 SS SUSTIVA EFAVIRENZ 1 Transplacental 400 MG, QD U U 0 400 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
87843444 8784344 1 Product used for unknown indication
87843444 8784344 2 Product used for unknown indication
87843444 8784344 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
87843444 8784344 CA
87843444 8784344 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
87843444 8784344 Foetal exposure during pregnancy
87843444 8784344 Turner'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
87843444 8784344 1 2011 0
87843444 8784344 3 2011 0