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
125185522 12518552 2 F 20160725 20160630 20160808 EXP US-GLAXOSMITHKLINE-US2016086723 GLAXOSMITHKLINE 0.00 M Y 0.00000 20160808 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
125185522 12518552 1 PS FLOVENT FLUTICASONE PROPIONATE 1 Respiratory (inhalation) 3 PUFF(S), TID U RV6X 21433 3 DF TID
125185522 12518552 2 SS FLOVENT FLUTICASONE PROPIONATE 1 UNK U EV7Y 21433
125185522 12518552 3 SS FLOVENT FLUTICASONE PROPIONATE 1 UNK U N22M 21433
125185522 12518552 4 SS VENTOLIN HFA ALBUTEROL SULFATE 1 Respiratory (inhalation) UNK U 0
125185522 12518552 5 C ATROVENT IPRATROPIUM BROMIDE 1 0
125185522 12518552 6 C LIPITOR ATORVASTATIN CALCIUM 1 0
125185522 12518552 7 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125185522 12518552 1 Asthma
125185522 12518552 4 Asthma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125185522 12518552 Device use error
125185522 12518552 Dyspnoea
125185522 12518552 Product quality issue

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

no results found

Therapies reported

no results found