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
123855766 12385576 6 F 2014 20160628 20160519 20160701 EXP US-GLAXOSMITHKLINE-US2016063142 GLAXOSMITHKLINE 0.00 F Y 0.00000 20160701 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
123855766 12385576 1 PS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), BID U 5ZP2553 21077 1 DF INHALATION POWDER BID
123855766 12385576 2 SS VENTOLIN HFA ALBUTEROL SULFATE 1 Respiratory (inhalation) 2-3 PUFFS PRN U UNKNOWN 0
123855766 12385576 3 SS DALIRESP ROFLUMILAST 1 U UNKNOWN 0
123855766 12385576 4 C LANOXIN DIGOXIN 1 0
123855766 12385576 5 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 0
123855766 12385576 6 C CARVEDILOL. CARVEDILOL 1 0
123855766 12385576 7 C GABAPENTIN. GABAPENTIN 1 0
123855766 12385576 8 C PREDNISONE. PREDNISONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123855766 12385576 1 Dyspnoea
123855766 12385576 2 Dyspnoea
123855766 12385576 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123855766 12385576 OT
123855766 12385576 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123855766 12385576 Chest injury
123855766 12385576 Drug ineffective
123855766 12385576 Dyspnoea
123855766 12385576 Incorrect dose administered
123855766 12385576 Malaise
123855766 12385576 Oral candidiasis
123855766 12385576 Pain
123855766 12385576 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