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
127730981 12773098 1 I 20110204 20160721 20160922 20160922 EXP US-ASTRAZENECA-2016SF00509 ASTRAZENECA 2.00 MON M Y 0.00000 20160922 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
127730981 12773098 1 PS SYNAGIS PALIVIZUMAB 1 Intramuscular 39 MG UNKNOWN 0 INJECTION
127730981 12773098 2 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 58 MG UNKNOWN 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127730981 12773098 1 Antiviral prophylaxis
127730981 12773098 2 Antiviral prophylaxis

Outcome of event

Event ID CASEID OUTC COD
127730981 12773098 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127730981 12773098 Bronchiolitis

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
127730981 12773098 1 20110204 20110204 0
127730981 12773098 2 20110314 20110314 0