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
127817671 12781767 1 I 200912 20110330 20160926 20160926 EXP US-ASTRAZENECA-2016SF02124 ASTRAZENECA 2.00 MON M Y 0.00000 20160926 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
127817671 12781767 1 PS SYNAGIS PALIVIZUMAB 1 Intramuscular U U UNKNOWN 0 50 MG INJECTION
127817671 12781767 2 SS SYNAGIS PALIVIZUMAB 1 Intramuscular U U UNKNOWN 0 50 MG INJECTION
127817671 12781767 3 SS SYNAGIS PALIVIZUMAB 1 Intramuscular U U UNKNOWN 0 50 MG INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127817671 12781767 1 Antiviral prophylaxis
127817671 12781767 2 Antiviral prophylaxis
127817671 12781767 3 Antiviral prophylaxis

Outcome of event

Event ID CASEID OUTC COD
127817671 12781767 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127817671 12781767 Bronchiolitis
127817671 12781767 Bronchitis
127817671 12781767 Lung disorder
127817671 12781767 Oxygen saturation decreased
127817671 12781767 Respiratory syncytial virus test positive
127817671 12781767 Wheezing

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
127817671 12781767 1 20091222 20091222 0
127817671 12781767 2 20100119 20100119 0
127817671 12781767 3 20100212 20100212 0