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
119281652 11928165 2 F 20160830 20160119 20160906 EXP GB-VIIV HEALTHCARE LIMITED-GB2016004186 VIIV 0.00 N Y 0.00000 20160906 OT GB GB

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
119281652 11928165 1 PS RETROVIR ZIDOVUDINE 1 Transplacental 500 MG, QD U 19655 500 MG QD
119281652 11928165 2 SS NEVIRAPINE. NEVIRAPINE 1 Transplacental 400 MG, QD U 0 400 MG QD
119281652 11928165 3 SS VIDEX DIDANOSINE 1 Transplacental 400 MG, QD U 0 400 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119281652 11928165 1 Product used for unknown indication
119281652 11928165 2 Product used for unknown indication
119281652 11928165 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119281652 11928165 OT
119281652 11928165 DE
119281652 11928165 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
119281652 11928165 Brain malformation
119281652 11928165 Congenital central nervous system anomaly
119281652 11928165 Death
119281652 11928165 Foetal exposure during pregnancy
119281652 11928165 Pulmonary hypoplasia

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
119281652 11928165 1 200001 0
119281652 11928165 2 20000122 0
119281652 11928165 3 20040122 0