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
126916721 12691672 1 I 201605 20160818 20160826 20160826 EXP AU-REGENERON PHARMACEUTICALS, INC.-2016-20954 REGENERON 0.00 Y 0.00000 20160826 CN AU AU

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
126916721 12691672 1 PS EYLEA AFLIBERCEPT 1 Intraocular 2 MG, UNK U UNKNOWN 125387 2 MG INJECTION
126916721 12691672 2 SS VENTOLIN ALBUTEROL SULFATE 1 UNK U U 0
126916721 12691672 3 SS VENTOLIN ALBUTEROL SULFATE 1 U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126916721 12691672 1 Neovascular age-related macular degeneration
126916721 12691672 2 Upper respiratory tract infection
126916721 12691672 3 Asthma

Outcome of event

Event ID CASEID OUTC COD
126916721 12691672 OT
126916721 12691672 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126916721 12691672 Asthma
126916721 12691672 Biliary colic
126916721 12691672 Dyspnoea
126916721 12691672 Ill-defined disorder
126916721 12691672 Influenza
126916721 12691672 Interstitial lung disease
126916721 12691672 Lung infection
126916721 12691672 Pain
126916721 12691672 Upper 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
126916721 12691672 1 20140110 0
126916721 12691672 2 201605 0