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
127770091 12777009 1 I 20081210 20100203 20160923 20160923 EXP US-ASTRAZENECA-2016SF00965 ASTRAZENECA 218.00 DY M Y 0.00000 20160924 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
127770091 12777009 1 PS SYNAGIS PALIVIZUMAB 1 Intramuscular 86 MG U U UNKNOWN 0 INJECTION
127770091 12777009 2 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 100 MG U U UNKNOWN 0 INJECTION
127770091 12777009 3 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 100 MG U U UNKNOWN 0 INJECTION
127770091 12777009 4 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 100 MG U U UNKNOWN 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127770091 12777009 1 Antiviral prophylaxis
127770091 12777009 2 Antiviral prophylaxis
127770091 12777009 3 Antiviral prophylaxis
127770091 12777009 4 Antiviral prophylaxis

Outcome of event

Event ID CASEID OUTC COD
127770091 12777009 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127770091 12777009 Body temperature increased
127770091 12777009 Growth retardation
127770091 12777009 Restlessness
127770091 12777009 Screaming
127770091 12777009 Upper respiratory tract 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
127770091 12777009 1 20081210 20081210 0
127770091 12777009 2 20090113 20090113 0
127770091 12777009 3 20090211 20090211 0
127770091 12777009 4 20090312 20090312 0