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
127953921 12795392 1 I 20160923 20160927 20160929 20160929 PER US-GLAXOSMITHKLINE-US2016141631 GLAXOSMITHKLINE 66.03 YR F Y 0.00000 20160929 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
127953921 12795392 1 PS FLOVENT DISKUS FLUTICASONE PROPIONATE 1 Respiratory (inhalation) 1 PUFF(S), BID Y Y34L 21433 1 DF BID
127953921 12795392 2 SS FLOVENT DISKUS FLUTICASONE PROPIONATE 1 Y 21433
127953921 12795392 3 SS FLOVENT DISKUS FLUTICASONE PROPIONATE 1 Y 21433
127953921 12795392 4 C CALCIUM CALCIUM 1 U 0
127953921 12795392 5 C CLARITIN LORATADINE 1 U 0
127953921 12795392 6 C IRBESARTAN AND HYDROCHLOROTHIAZIDE HYDROCHLOROTHIAZIDEIRBESARTAN 1 U 0
127953921 12795392 7 C LEVOTHYROXIN LEVOTHYROXINE 1 U 0
127953921 12795392 8 C SINGULAIR MONTELUKAST SODIUM 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127953921 12795392 1 Dyspnoea
127953921 12795392 2 Wheezing
127953921 12795392 3 Cough

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127953921 12795392 Cough
127953921 12795392 Dyspnoea
127953921 12795392 Haemoptysis
127953921 12795392 Hypersensitivity
127953921 12795392 Wheezing

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
127953921 12795392 1 20160923 20160926 0