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
126916121 12691612 1 I 20160822 20160826 20160826 EXP US-ABBVIE-16P-163-1708920-00 ABBVIE 0.00 F Y 0.00000 20160826 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
126916121 12691612 1 PS RITONAVIR. RITONAVIR 1 Transplacental UNKNOWN 20945
126916121 12691612 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental UNKNOWN 0
126916121 12691612 3 SS ATAZANAVIR SULFATE ATAZANAVIR SULFATE 1 Transplacental UNKNOWN 0
126916121 12691612 4 SS TIVICAY DOLUTEGRAVIR SODIUM 1 Transplacental UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126916121 12691612 1 Maternal exposure timing unspecified
126916121 12691612 2 Maternal exposure timing unspecified
126916121 12691612 3 Maternal exposure timing unspecified
126916121 12691612 4 Maternal exposure timing unspecified

Outcome of event

Event ID CASEID OUTC COD
126916121 12691612 CA
126916121 12691612 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126916121 12691612 Foetal exposure during pregnancy
126916121 12691612 Patent ductus arteriosus
126916121 12691612 Premature baby

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

no results found

Therapies reported

no results found