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
124384223 12438422 3 F 20160531 20160718 20160606 20160721 EXP US-GLAXOSMITHKLINE-US2016079500 GLAXOSMITHKLINE 71.89 YR F Y 0.00000 20160721 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
124384223 12438422 1 PS FLOVENT FLUTICASONE PROPIONATE 1 Respiratory (inhalation) 2 PUFF(S), BID M52W 21433 2 DF BID
124384223 12438422 2 SS VENTOLIN ALBUTEROL SULFATE 1 Respiratory (inhalation) 2-4 PUFF(S), PRN 6ZP4756 0
124384223 12438422 3 C QUINAPRIL. QUINAPRIL 1 0
124384223 12438422 4 C LEVOTHYROXINE. LEVOTHYROXINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124384223 12438422 1 Chronic obstructive pulmonary disease
124384223 12438422 2 Asthma

Outcome of event

Event ID CASEID OUTC COD
124384223 12438422 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124384223 12438422 Accidental exposure to product
124384223 12438422 Cataract
124384223 12438422 Cataract operation
124384223 12438422 Device leakage
124384223 12438422 Device use error
124384223 12438422 Incorrect product storage
124384223 12438422 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