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
127818301 12781830 1 I 20101029 20160721 20160926 20160926 EXP US-ASTRAZENECA-2016SF02217 ASTRAZENECA 7.53 MON F Y 0.00000 20160927 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
127818301 12781830 1 PS SYNAGIS PALIVIZUMAB 1 Intramuscular UNKNOWN 0 100 MG INJECTION
127818301 12781830 2 SS SYNAGIS PALIVIZUMAB 1 Intramuscular UNKNOWN 0 100 MG INJECTION
127818301 12781830 3 SS SYNAGIS PALIVIZUMAB 1 Intramuscular UNKNOWN 0 100 MG INJECTION
127818301 12781830 4 SS SYNAGIS PALIVIZUMAB 1 Intramuscular UNKNOWN 0 100 MG INJECTION
127818301 12781830 5 SS SYNAGIS PALIVIZUMAB 1 Intramuscular UNKNOWN 0 150 MG INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127818301 12781830 1 Bronchopulmonary dysplasia
127818301 12781830 2 Bronchopulmonary dysplasia
127818301 12781830 3 Bronchopulmonary dysplasia
127818301 12781830 4 Bronchopulmonary dysplasia
127818301 12781830 5 Bronchopulmonary dysplasia

Outcome of event

Event ID CASEID OUTC COD
127818301 12781830 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127818301 12781830 Pneumonia viral

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
127818301 12781830 1 20101006 20101006 0
127818301 12781830 2 20101103 20101103 0
127818301 12781830 3 20101201 20101201 0
127818301 12781830 4 20101230 20101230 0
127818301 12781830 5 20110126 20110126 0