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
127684691 12768469 1 I 200903 20100203 20160921 20160921 EXP US-ASTRAZENECA-2016SF00157 ASTRAZENECA 9.00 MON M Y 0.00000 20160921 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
127684691 12768469 1 PS SYNAGIS PALIVIZUMAB 1 Intramuscular 55 MG U U 0 INJECTION
127684691 12768469 2 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 85 MG U U 0 INJECTION
127684691 12768469 3 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 101 MG U U 0 INJECTION
127684691 12768469 4 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 108 MG U U 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127684691 12768469 1 Antiviral prophylaxis
127684691 12768469 2 Antiviral prophylaxis
127684691 12768469 3 Antiviral prophylaxis
127684691 12768469 4 Antiviral prophylaxis

Outcome of event

Event ID CASEID OUTC COD
127684691 12768469 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127684691 12768469 Pneumonia
127684691 12768469 Respiratory syncytial virus 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
127684691 12768469 1 20080925 20080925 0
127684691 12768469 2 20081128 20081128 0
127684691 12768469 3 20090113 20090113 0
127684691 12768469 4 20090224 20090224 0