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
125424472 12542447 2 F 20160616 20160628 20160708 20160711 EXP US-ASTRAZENECA-2016SE73170 ASTRAZENECA 3.00 MON M Y 6.10000 KG 20160711 CN CO CO

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
125424472 12542447 1 PS SYNAGIS PALIVIZUMAB 1 Intramuscular 30 UG/KG Y 0 15 UG/KG INJECTION /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125424472 12542447 1 Bronchopulmonary dysplasia

Outcome of event

Event ID CASEID OUTC COD
125424472 12542447 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125424472 12542447 Bronchiolitis

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
125424472 12542447 1 20160407 20160512 0