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
125831691 12583169 1 I 2014 20160708 20160722 20160722 EXP US-GLAXOSMITHKLINE-US2016098063 GLAXOSMITHKLINE 0.00 F Y 0.00000 20160722 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
125831691 12583169 1 PS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), QD 6ZP3932 21077 1 DF INHALATION POWDER QD
125831691 12583169 2 SS VENTOLIN HFA ALBUTEROL SULFATE 1 Respiratory (inhalation) UNK U 6ZP5557 0
125831691 12583169 3 C LOESTRIN NOS ETHINYL ESTRADIOLNORETHINDRONE ACETATE 1 0
125831691 12583169 4 C SINGULAIR MONTELUKAST SODIUM 1 0
125831691 12583169 5 C XYZAL LEVOCETIRIZINE DIHYDROCHLORIDE 1 0
125831691 12583169 6 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 0
125831691 12583169 7 C MOMETASONE FUROATE MONOHYDRATE. MOMETASONE FUROATE MONOHYDRATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125831691 12583169 1 Asthma
125831691 12583169 2 Asthma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125831691 12583169 Asthma
125831691 12583169 Device use error
125831691 12583169 Drug ineffective
125831691 12583169 Intentional product use issue
125831691 12583169 Treatment noncompliance
125831691 12583169 Wrong technique in product usage process

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
125831691 12583169 1 2002 0