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
127814411 12781441 1 I 200911 20110330 20160926 20160926 EXP US-ASTRAZENECA-2016SF02224 ASTRAZENECA 11.00 MON M Y 0.00000 20160926 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
127814411 12781441 1 PS SYNAGIS PALIVIZUMAB 1 Intramuscular U U UNKNOWN 0 100 MG INJECTION /month
127814411 12781441 2 SS SYNAGIS PALIVIZUMAB 1 Intramuscular U U UNKNOWN 0 100 MG INJECTION /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127814411 12781441 1 Antiviral prophylaxis
127814411 12781441 2 Antiviral prophylaxis

Outcome of event

Event ID CASEID OUTC COD
127814411 12781441 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127814411 12781441 Bronchitis
127814411 12781441 Respiratory syncytial virus test positive

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
127814411 12781441 1 20091009 20091202 0
127814411 12781441 2 20100114 20100224 0