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
125925042 12592504 2 F 20160307 20160808 20160726 20160810 EXP FR-JNJFOC-20160717483 JANSSEN -0.22 YR F Y 2.96000 KG 20160810 OT FR FR

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
125925042 12592504 1 PS PREZISTA DARUNAVIR ETHANOLATE 1 Transplacental N 21976 800 MG TABLETS QD
125925042 12592504 2 SS NORVIR RITONAVIR 1 Transplacental 0 100 MG CAPSULE QD
125925042 12592504 3 SS AMOXICILLIN TRIHYDRATE AMOXICILLIN 1 Transplacental 0 UNSPECIFIED
125925042 12592504 4 SS DOLIPRANE ACETAMINOPHEN 1 Transplacental 0 UNSPECIFIED
125925042 12592504 5 SS SMECTA MONTMORILLONITE 1 Transplacental 0 POWDER

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125925042 12592504 1 HIV infection
125925042 12592504 2 HIV infection
125925042 12592504 3 Product used for unknown indication
125925042 12592504 4 Product used for unknown indication
125925042 12592504 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125925042 12592504 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125925042 12592504 Foetal exposure during pregnancy
125925042 12592504 Macrosomia

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
125925042 12592504 1 20160526 0
125925042 12592504 2 20160526 0
125925042 12592504 3 20160204 0
125925042 12592504 4 20160204 0
125925042 12592504 5 20160204 0