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
115711513 11571151 3 F 2008 20160725 20150929 20160811 EXP US-GLAXOSMITHKLINE-US2015GSK116586 GLAXOSMITHKLINE 0.00 F Y 0.00000 20160811 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
115711513 11571151 1 PS FLOVENT FLUTICASONE PROPIONATE 1 Respiratory (inhalation) 2 PUFF(S), BID YT8N 21433 2 DF BID
115711513 11571151 2 SS FLOVENT FLUTICASONE PROPIONATE 1 Respiratory (inhalation) 1 PUFF(S), BID 21433 1 DF BID
115711513 11571151 3 SS FLOVENT FLUTICASONE PROPIONATE 1 Respiratory (inhalation) 2 PUFF(S), BID 21433 2 DF BID
115711513 11571151 4 SS FLOVENT FLUTICASONE PROPIONATE 1 Respiratory (inhalation) 1 PUFF(S), BID 21433 1 DF BID
115711513 11571151 5 SS FLOVENT FLUTICASONE PROPIONATE 1 Respiratory (inhalation) 2 PUFF(S), BID NW9U 21433 2 DF BID
115711513 11571151 6 SS SEREVENT DISKUS SALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), BID 5ZP8914 0 1 DF INHALATION POWDER BID
115711513 11571151 7 SS SEREVENT DISKUS SALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), QD 0 1 DF INHALATION POWDER QD
115711513 11571151 8 SS SEREVENT DISKUS SALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), BID 0 1 DF INHALATION POWDER BID
115711513 11571151 9 SS SEREVENT DISKUS SALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), QD 0 1 DF INHALATION POWDER QD
115711513 11571151 10 SS SEREVENT DISKUS SALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), BID 6ZP3530 0 1 DF INHALATION POWDER BID
115711513 11571151 11 C DIGOXIN. DIGOXIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115711513 11571151 1 Asthma
115711513 11571151 2 Chronic obstructive pulmonary disease
115711513 11571151 6 Asthma
115711513 11571151 7 Chronic obstructive pulmonary disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
115711513 11571151 Angiogram
115711513 11571151 Asthma
115711513 11571151 Chronic obstructive pulmonary disease
115711513 11571151 Drug dose omission
115711513 11571151 Heart rate abnormal
115711513 11571151 Humidity intolerance
115711513 11571151 Inability to afford medication
115711513 11571151 Inappropriate schedule of drug administration
115711513 11571151 Incorrect dose administered
115711513 11571151 Intentional product use issue
115711513 11571151 Multiple allergies
115711513 11571151 Stress

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
115711513 11571151 1 1996 0
115711513 11571151 3 201601 0
115711513 11571151 4 201601 20160401 0
115711513 11571151 5 201604 0
115711513 11571151 6 1996 0
115711513 11571151 8 201601 0
115711513 11571151 9 201601 20160401 0
115711513 11571151 10 201604 0