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
125361672 12536167 2 F 20160627 20160707 20160916 PER US-GLAXOSMITHKLINE-US2016092049 GLAXOSMITHKLINE 0.00 M Y 0.00000 20160916 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
125361672 12536167 1 PS ANORO ELLIPTA UMECLIDINIUM BROMIDEVILANTEROL TRIFENATATE 1 Respiratory (inhalation) 1 PUFF(S), QD 5ZP2634 203975 1 DF INHALATION POWDER QD
125361672 12536167 2 SS VENTOLIN HFA ALBUTEROL SULFATE 1 Respiratory (inhalation) 1PUFF 2 TO 4 TIMES DAILY 6ZP4400 0 1 DF
125361672 12536167 3 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) UNK UNKNOWN 0
125361672 12536167 4 C SYSTANE ULTRA POLYETHYLENE GLYCOL 400PROPYLENE GLYCOL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125361672 12536167 1 Chronic obstructive pulmonary disease
125361672 12536167 2 Productive cough
125361672 12536167 3 Chronic obstructive pulmonary disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125361672 12536167 Adverse drug reaction
125361672 12536167 Constipation
125361672 12536167 Drug ineffective
125361672 12536167 Dysphonia
125361672 12536167 Eye swelling
125361672 12536167 Respiratory disorder
125361672 12536167 Throat tightness

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
125361672 12536167 1 201606 0
125361672 12536167 2 2001 0
125361672 12536167 3 2013 201606 0