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
127549582 12754958 2 F 20160919 20160916 20160926 EXP US-ABBVIE-16P-163-1725906-00 ABBVIE 0.00 M Y 0.00000 20160926 OT COUNTRY NOT SPECIFIED 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
127549582 12754958 1 PS NORVIR RITONAVIR 1 Transplacental D UNKNOWN 22417
127549582 12754958 2 SS TRUVADA TM EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental D UNKNOWN 0
127549582 12754958 3 SS PREZISTA DARUNAVIR ETHANOLATE 1 Transplacental D UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127549582 12754958 1 Maternal exposure timing unspecified
127549582 12754958 2 Maternal exposure timing unspecified
127549582 12754958 3 Maternal exposure timing unspecified

Outcome of event

Event ID CASEID OUTC COD
127549582 12754958 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
127549582 12754958 Foetal exposure during pregnancy
127549582 12754958 Renal aplasia
127549582 12754958 Umbilical cord abnormality

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found