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
127684021 12768402 1 I 20100203 20160921 20160921 EXP US-ASTRAZENECA-2016SF00147 ASTRAZENECA 0.00 M Y 0.00000 20160921 MD DE DE

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
127684021 12768402 1 PS SYNAGIS PALIVIZUMAB 1 Intramuscular 50 MG U U 0 INJECTION
127684021 12768402 2 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 50 MG U U 0 INJECTION
127684021 12768402 3 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 60 MG U U 0 INJECTION
127684021 12768402 4 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 70 MG U U 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127684021 12768402 1 Premature baby
127684021 12768402 2 Premature baby
127684021 12768402 3 Premature baby
127684021 12768402 4 Premature baby

Outcome of event

Event ID CASEID OUTC COD
127684021 12768402 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127684021 12768402 Pneumonia
127684021 12768402 Respiratory syncytial virus test positive

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
127684021 12768402 1 20090123 20090123 0
127684021 12768402 2 20090218 20090218 0
127684021 12768402 3 20090319 20090319 0
127684021 12768402 4 20090416 20090416 0