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
125850351 12585035 1 I 201602 20160527 20160723 20160723 EXP US-ASTRAZENECA-2016SE59506 ASTRAZENECA 8.00 MON F Y 6.80000 KG 20160723 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
125850351 12585035 1 PS SYNAGIS PALIVIZUMAB 1 Intramuscular U 0 50 MG INJECTION
125850351 12585035 2 SS SYNAGIS PALIVIZUMAB 1 Intramuscular U 0 75 MG INJECTION
125850351 12585035 3 SS SYNAGIS PALIVIZUMAB 1 Intramuscular U 0 100 MG INJECTION
125850351 12585035 4 SS SYNAGIS PALIVIZUMAB 1 Intramuscular U 0 100 MG INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125850351 12585035 1 Antiviral prophylaxis
125850351 12585035 2 Antiviral prophylaxis
125850351 12585035 3 Antiviral prophylaxis
125850351 12585035 4 Antiviral prophylaxis

Outcome of event

Event ID CASEID OUTC COD
125850351 12585035 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125850351 12585035 Bronchitis
125850351 12585035 Fluid intake reduced
125850351 12585035 Nasopharyngitis
125850351 12585035 Otitis media
125850351 12585035 Respiratory tract 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
125850351 12585035 1 20150928 20150928 0
125850351 12585035 2 20151026 20151026 0
125850351 12585035 3 20151221 20151221 0
125850351 12585035 4 20160115 20160115 0