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
100598796 10059879 6 F 20130320 20160824 20140404 20160829 EXP US-GLAXOSMITHKLINE-A1066920A GLAXOSMITHKLINE 28.39 YR M Y 0.00000 20160829 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
100598796 10059879 1 PS VENTOLIN ALBUTEROL SULFATE 1 Respiratory (inhalation) 2 PUFFS AS REQUIRED U UNKNOWN 20983 2 DF
100598796 10059879 2 SS ALBUTEROL. ALBUTEROL 1 U 20983

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100598796 10059879 1 Asthma
100598796 10059879 2 Asthma

Outcome of event

Event ID CASEID OUTC COD
100598796 10059879 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100598796 10059879 Abdominal discomfort
100598796 10059879 Asthma
100598796 10059879 Choking
100598796 10059879 Drug ineffective
100598796 10059879 Emotional distress
100598796 10059879 Fall
100598796 10059879 Fear
100598796 10059879 Foreign body
100598796 10059879 Impaired work ability
100598796 10059879 Loss of consciousness
100598796 10059879 Mouth haemorrhage
100598796 10059879 Oropharyngeal pain
100598796 10059879 Product quality issue
100598796 10059879 Pulmonary function test decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found