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
113288034 11328803 4 F 20160701 20150731 20160707 EXP US-ABBVIE-15P-163-1434364-00 ABBVIE 0.00 F Y 0.00000 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
113288034 11328803 1 PS NORVIR RITONAVIR 1 Transplacental UNKNOWN 20945
113288034 11328803 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental UNKNOWN 0
113288034 11328803 3 SS PREZISTA DARUNAVIR ETHANOLATE 1 Transplacental UNKNOWN 0
113288034 11328803 4 SS TIVICAY DOLUTEGRAVIR SODIUM 1 Transplacental UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113288034 11328803 1 Maternal exposure timing unspecified
113288034 11328803 2 Maternal exposure timing unspecified
113288034 11328803 3 Maternal exposure timing unspecified
113288034 11328803 4 Maternal exposure timing unspecified

Outcome of event

Event ID CASEID OUTC COD
113288034 11328803 OT
113288034 11328803 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
113288034 11328803 Cerebral calcification
113288034 11328803 Foetal exposure during pregnancy
113288034 11328803 Foetal growth restriction

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

no results found

Therapies reported

no results found