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
127564231 12756423 1 I 20100225 20110330 20160916 20160916 EXP US-ASTRAZENECA-2016SE97916 ASTRAZENECA 3.97 MON M Y 0.90000 KG 20160917 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
127564231 12756423 1 PS SYNAGIS PALIVIZUMAB 1 Intramuscular 0 50 MG INJECTION
127564231 12756423 2 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 0 50 MG INJECTION
127564231 12756423 3 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 0 50 MG INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127564231 12756423 1 Premature baby
127564231 12756423 2 Premature baby
127564231 12756423 3 Premature baby

Outcome of event

Event ID CASEID OUTC COD
127564231 12756423 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127564231 12756423 Bronchitis
127564231 12756423 Respiratory syncytial virus 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
127564231 12756423 1 20100110 20100110 0
127564231 12756423 2 20100204 20100204 0
127564231 12756423 3 20100302 20100302 0