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
125243724 12524372 4 F 20150913 20160802 20160704 20160812 EXP US-ASTRAZENECA-2016SE72202 ASTRAZENECA 515.00 DY F Y 0.00000 20160812 MD JP JP

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
125243724 12524372 1 PS SYNAGIS PALIVIZUMAB 1 Intramuscular 90.0MG UNKNOWN U U 0 90 MG INJECTION
125243724 12524372 2 SS SYNAGIS PALIVIZUMAB 1 Intramuscular 90.0MG UNKNOWN U U 0 90 MG INJECTION
125243724 12524372 3 C FERRIC PYROPHOSPHATE FERRIC PYROPHOSPHATE 1 Oral 0 SYRUP
125243724 12524372 4 C FAMOTIDINE. FAMOTIDINE 1 Oral 0
125243724 12524372 5 C FUROSEMIDE. FUROSEMIDE 1 Oral 0 GRANULES
125243724 12524372 6 C SPIRONOLACTONE. SPIRONOLACTONE 1 Oral 0 GRANULES

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125243724 12524372 1 Antiviral prophylaxis
125243724 12524372 2 Bronchopulmonary dysplasia
125243724 12524372 3 Product used for unknown indication
125243724 12524372 4 Product used for unknown indication
125243724 12524372 5 Product used for unknown indication
125243724 12524372 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125243724 12524372 OT
125243724 12524372 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125243724 12524372 Bronchitis
125243724 12524372 Pneumonia
125243724 12524372 Respiratory failure

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
125243724 12524372 1 20150902 0
125243724 12524372 2 20150902 0