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
106443985 10644398 5 F 20160801 20141210 20160803 EXP US-GLAXOSMITHKLINE-US2014GSK033502 GLAXOSMITHKLINE 0.00 F Y 0.00000 20160803 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
106443985 10644398 1 PS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown UNK, U U AZP6389 21077 INHALATION POWDER
106443985 10644398 2 SS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 UNK U 4ZP6473 21077 INHALATION POWDER
106443985 10644398 3 SS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 UNK U 5ZT2436 21077 INHALATION POWDER
106443985 10644398 4 SS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 UNK U 5ZP2436 21077 INHALATION POWDER
106443985 10644398 5 SS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 UNK U UNKNOWN 21077 INHALATION POWDER
106443985 10644398 6 SS VENTOLIN HFA ALBUTEROL SULFATE 1 Unknown UNK, U U KY4C 0
106443985 10644398 7 SS VENTOLIN HFA ALBUTEROL SULFATE 1 UNK U UNKNOWN 0
106443985 10644398 8 SS ANORO ELLIPTA UMECLIDINIUM BROMIDEVILANTEROL TRIFENATATE 1 UNK U UNKNOWN 0 INHALATION POWDER
106443985 10644398 9 SS ANORO ELLIPTA UMECLIDINIUM BROMIDEVILANTEROL TRIFENATATE 1 U 0 INHALATION POWDER
106443985 10644398 10 SS SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Unknown UNK, U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106443985 10644398 1 Asthma
106443985 10644398 2 Chronic obstructive pulmonary disease
106443985 10644398 6 Chronic obstructive pulmonary disease
106443985 10644398 7 Asthma
106443985 10644398 8 Chronic obstructive pulmonary disease
106443985 10644398 9 Asthma
106443985 10644398 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
106443985 10644398 HO
106443985 10644398 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106443985 10644398 Bronchitis
106443985 10644398 Colostomy
106443985 10644398 Dehydration
106443985 10644398 Drug dose omission
106443985 10644398 Gastric disorder
106443985 10644398 Lower respiratory tract congestion
106443985 10644398 Malaise
106443985 10644398 Pneumonia
106443985 10644398 Vasculitis
106443985 10644398 Vomiting

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
106443985 10644398 1 2009 0
106443985 10644398 5 2008 0
106443985 10644398 7 2008 0
106443985 10644398 8 2008 0