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
127818141 12781814 1 I 201012 20110721 20160926 20160926 EXP US-ASTRAZENECA-2016SF02191 ASTRAZENECA 4.23 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
127818141 12781814 1 PS SYNAGIS PALIVIZUMAB 1 Intramuscular 57 MG U U 0 INJECTION
127818141 12781814 2 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 66 MG U U 0 INJECTION
127818141 12781814 3 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 78 MG U U 0 INJECTION
127818141 12781814 4 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 137 MG U U 0 INJECTION
127818141 12781814 5 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 140 MG U U 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127818141 12781814 1 Antiviral prophylaxis
127818141 12781814 2 Antiviral prophylaxis
127818141 12781814 3 Antiviral prophylaxis
127818141 12781814 4 Antiviral prophylaxis
127818141 12781814 5 Antiviral prophylaxis

Outcome of event

Event ID CASEID OUTC COD
127818141 12781814 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127818141 12781814 Bronchitis
127818141 12781814 Pneumonia respiratory syncytial 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
127818141 12781814 1 20101105 20101105 0
127818141 12781814 2 20101206 20101206 0
127818141 12781814 3 20110119 20110119 0
127818141 12781814 4 20110217 20110217 0
127818141 12781814 5 20110314 20110314 0