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
126044141 12604414 1 I 201607 20160722 20160728 20160728 EXP US-GLAXOSMITHKLINE-US2016106891 GLAXOSMITHKLINE 0.00 F Y 0.00000 20160728 CN US US

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
126044141 12604414 1 PS FLONASE FLUTICASONE PROPIONATE 1 UNK U UNK 205434 NASAL SPRAY
126044141 12604414 2 SS FLONASE FLUTICASONE PROPIONATE 1 U 205434 NASAL SPRAY
126044141 12604414 3 SS KEFLEX CEPHALEXIN 1 UNK U UNK 0
126044141 12604414 4 SS KEFLEX CEPHALEXIN 1 U 0
126044141 12604414 5 SS AMOXIL AMOXICILLIN 1 UNK U UNK 0
126044141 12604414 6 SS AMOXIL AMOXICILLIN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126044141 12604414 1 Ear infection
126044141 12604414 2 Middle ear effusion
126044141 12604414 3 Ear infection
126044141 12604414 4 Middle ear effusion
126044141 12604414 5 Ear infection
126044141 12604414 6 Middle ear effusion

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126044141 12604414 Drug ineffective
126044141 12604414 Exposure during pregnancy
126044141 12604414 Intentional product misuse

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
126044141 12604414 1 201607 0
126044141 12604414 3 201607 0
126044141 12604414 5 201607 0