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
125264971 12526497 1 I 20150811 20151104 20160705 20160705 EXP US-SUN PHARMACEUTICAL INDUSTRIES LTD-2015US-106226 RANBAXY 39.00 DY M Y 3035.00000 KG 20160705 CN US 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
125264971 12526497 1 PS ZIDOVUDINE. ZIDOVUDINE 1 Transplacental 600 MG, DAILY Y 77327 600 MG
125264971 12526497 2 SS COMPLERA EMTRICITABINERILPIVIRINE HYDROCHLORIDETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental UNK Y 0
125264971 12526497 3 SS PREZISTA DARUNAVIR ETHANOLATE 1 Transplacental UNK Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125264971 12526497 1 HIV infection
125264971 12526497 2 HIV infection
125264971 12526497 3 HIV infection

Outcome of event

Event ID CASEID OUTC COD
125264971 12526497 OT
125264971 12526497 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125264971 12526497 Foetal exposure during pregnancy
125264971 12526497 Infantile vomiting
125264971 12526497 Jaundice
125264971 12526497 Jaundice neonatal
125264971 12526497 Meconium in amniotic fluid
125264971 12526497 Vomiting
125264971 12526497 Weight decrease neonatal
125264971 12526497 Weight decreased

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
125264971 12526497 1 20150226 0
125264971 12526497 2 20150226 0
125264971 12526497 3 20150427 0