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
127607531 12760753 1 I 20081208 20160919 20160919 EXP US-ASTRAZENECA-2016SE99612 ASTRAZENECA 0.00 F Y 0.00000 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
127607531 12760753 1 PS SYNAGIS PALIVIZUMAB 1 Intramuscular DOSE AND FREQUENCY NOT REPORTED U U UNKNOWN 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127607531 12760753 1 Antiviral prophylaxis

Outcome of event

Event ID CASEID OUTC COD
127607531 12760753 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127607531 12760753 Bronchiolitis
127607531 12760753 Pneumonia respiratory syncytial viral

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found