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
126349991 12634999 1 I 20160614 20160729 20160809 20160809 EXP FR-JNJFOC-20160803212 JANSSEN 0.00 M Y 0.00000 20160809 CN FR FR

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
126349991 12634999 1 PS EVIPLERA EMTRICITABINERILPIVIRINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental N 0 1 DF TABLET QD
126349991 12634999 2 SS PREZISTA DARUNAVIR ETHANOLATE 1 Transplacental N 21976 TABLETS
126349991 12634999 3 SS NORVIR RITONAVIR 1 Transplacental 0 UNSPECIFIED
126349991 12634999 4 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126349991 12634999 1 HIV infection
126349991 12634999 2 HIV infection
126349991 12634999 3 HIV infection
126349991 12634999 4 HIV infection

Outcome of event

Event ID CASEID OUTC COD
126349991 12634999 OT
126349991 12634999 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
126349991 12634999 Foetal exposure during pregnancy
126349991 12634999 Talipes

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
126349991 12634999 1 20141103 20160504 0
126349991 12634999 2 2016 0
126349991 12634999 3 2016 0
126349991 12634999 4 2016 0