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
127972151 12797215 1 I 20101120 20110721 20160929 20160929 EXP US-ASTRAZENECA-2016SF03181 ASTRAZENECA 506.00 DY F Y 0.30000 KG 20160930 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
127972151 12797215 1 PS SYNAGIS PALIVIZUMAB 1 Intramuscular D UNKNOWN 0 100 MG INJECTION
127972151 12797215 2 SS SYNAGIS PALIVIZUMAB 1 Intramuscular D UNKNOWN 0 100 MG INJECTION
127972151 12797215 3 SS SYNAGIS PALIVIZUMAB 1 Intramuscular D UNKNOWN 0 100 MG INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127972151 12797215 1 Respiratory syncytial virus infection
127972151 12797215 2 Respiratory syncytial virus infection
127972151 12797215 3 Respiratory syncytial virus infection

Outcome of event

Event ID CASEID OUTC COD
127972151 12797215 HO
127972151 12797215 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127972151 12797215 Acute respiratory distress syndrome
127972151 12797215 Death
127972151 12797215 Pneumonia

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
127972151 12797215 1 20101004 20101004 0
127972151 12797215 2 20101206 20101206 0
127972151 12797215 3 20101103 20101103 0