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
127605621 12760562 1 I 20100209 20110330 20160919 20160919 EXP US-ASTRAZENECA-2016SE99604 ASTRAZENECA 176.00 DY M Y 0.90000 KG 20160919 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
127605621 12760562 1 PS SYNAGIS PALIVIZUMAB 1 Intramuscular 40 MG UNKNOWN 0 INJECTION
127605621 12760562 2 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 40 MG UNKNOWN 0 INJECTION
127605621 12760562 3 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 40 MG UNKNOWN 0 INJECTION
127605621 12760562 4 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 40 MG UNKNOWN 0 INJECTION
127605621 12760562 5 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 40 MG UNKNOWN 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127605621 12760562 1 Premature baby
127605621 12760562 2 Premature baby
127605621 12760562 3 Premature baby
127605621 12760562 4 Premature baby
127605621 12760562 5 Premature baby

Outcome of event

Event ID CASEID OUTC COD
127605621 12760562 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127605621 12760562 Respiratory syncytial virus infection
127605621 12760562 Rotavirus 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
127605621 12760562 1 20091110 20091110 0
127605621 12760562 2 20091202 20091202 0
127605621 12760562 3 20091223 20091223 0
127605621 12760562 4 20100115 20100115 0
127605621 12760562 5 20100420 20100420 0