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
126302272 12630227 2 F 20160701 20160824 20160808 20160901 EXP US-ASTRAZENECA-2016SE84955 ASTRAZENECA 303.00 DY F Y 8.00000 KG 20160901 OT CL CL

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
126302272 12630227 1 PS SYNAGIS PALIVIZUMAB 1 Intramuscular 1ST DOSE U 0 INJECTION
126302272 12630227 2 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 120MG, 2ND DOSE, MORE THAN 30 DAYS FROM FIRST DOSE U 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126302272 12630227 1 Antiviral prophylaxis
126302272 12630227 2 Antiviral prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126302272 12630227 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126302272 12630227 Bronchiolitis
126302272 12630227 Circumstance or information capable of leading to medication error
126302272 12630227 Respiratory syncytial virus infection

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
126302272 12630227 1 20160509 20160509 0
126302272 12630227 2 20160630 20160630 0