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
109334845 10933484 5 F 20160701 20150320 20160707 EXP US-ABBVIE-15P-163-1360568-00 ABBVIE 0.00 F Y 3.18000 KG 20160707 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
109334845 10933484 1 PS NORVIR RITONAVIR 1 Transplacental UNKNOWN 20945
109334845 10933484 2 SS REYATAZ ATAZANAVIR SULFATE 1 Transplacental UNKNOWN 0
109334845 10933484 3 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109334845 10933484 1 Maternal exposure timing unspecified
109334845 10933484 2 Maternal exposure timing unspecified
109334845 10933484 3 Maternal exposure timing unspecified

Outcome of event

Event ID CASEID OUTC COD
109334845 10933484 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
109334845 10933484 Double outlet right ventricle
109334845 10933484 Foetal exposure during pregnancy
109334845 10933484 Ventricular septal defect

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

no results found

Therapies reported

no results found