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
126297623 12629762 3 F 20160909 20160808 20160912 PER US-GLAXOSMITHKLINE-US2016107759 GLAXOSMITHKLINE 0.00 M Y 0.00000 20160912 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
126297623 12629762 1 PS VENTOLIN HFA ALBUTEROL SULFATE 1 Respiratory (inhalation) 2 PUFF(S), 1D 5ZP0293 20983 2 DF QD
126297623 12629762 2 SS VENTOLIN HFA ALBUTEROL SULFATE 1 20983
126297623 12629762 3 C Fluticasone Nasal spray FLUTICASONEFLUTICASONE PROPIONATE 1 0 NASAL SPRAY
126297623 12629762 4 C IBUPROFEN. IBUPROFEN 1 0
126297623 12629762 5 C MUCINEX GUAIFENESIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126297623 12629762 1 Seasonal allergy
126297623 12629762 2 Asthma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126297623 12629762 Device use error
126297623 12629762 Drug ineffective
126297623 12629762 Product quality issue
126297623 12629762 Underdose
126297623 12629762 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
126297623 12629762 1 2013 0