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
126886844 12688684 4 F 20160906 20160825 20160912 EXP BR-ABBVIE-16P-020-1710398-00 ABBVIE 0.00 M Y 0.00000 20160912 MD COUNTRY NOT SPECIFIED BR

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
126886844 12688684 1 PS KALETRA LOPINAVIRRITONAVIR 1 Transplacental UNKNOWN 21226
126886844 12688684 2 SS RETROVIR ZIDOVUDINE 1 Transplacental UNKNOWN 0
126886844 12688684 3 SS LAMIVUDINE W/TENOFOVIR DISOPROXIL LAMIVUDINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126886844 12688684 1 Maternal exposure timing unspecified
126886844 12688684 2 Maternal exposure timing unspecified
126886844 12688684 3 Maternal exposure timing unspecified

Outcome of event

Event ID CASEID OUTC COD
126886844 12688684 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
126886844 12688684 Foetal exposure during pregnancy
126886844 12688684 Hydrocephalus
126886844 12688684 Meningomyelocele

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

no results found

Therapies reported

no results found