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
127045141 12704514 1 I 20110816 20160823 20160831 20160831 EXP BR-GLAXOSMITHKLINE-BR2016GSK124927 GLAXOSMITHKLINE 89.82 YR F Y 0.00000 20160831 CN BR BR

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
127045141 12704514 1 PS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 2 PUFF(S), QD Y 21077 2 DF INHALATION POWDER QD
127045141 12704514 2 SS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 2 UNK, BID 0 2 DF OROMUCOSAL SPRAY BID
127045141 12704514 3 SS Marevan WARFARIN SODIUM 1 U U 0
127045141 12704514 4 C FUROSEMIDE. FUROSEMIDE 1 Oral U 0
127045141 12704514 5 C SPIRONOLACTONE. SPIRONOLACTONE 1 U 0
127045141 12704514 6 C QUETIAPINE. QUETIAPINE 1 Oral 25 MG, QD U 0 25 MG QD
127045141 12704514 7 C Atorvastatin ATORVASTATIN 1 Oral 1 UNK, QD U 0 1 DF QD
127045141 12704514 8 C ALPRAZOLAM. ALPRAZOLAM 1 Oral 0.5 MG, QD U 0 .5 MG QD
127045141 12704514 9 C LOSARTAN POTASSIUM. LOSARTAN POTASSIUM 1 Oral 1 UNK, QD U 0 1 DF QD
127045141 12704514 10 C MIRTAZAPINE. MIRTAZAPINE 1 Oral U 0
127045141 12704514 11 C OXYGEN. OXYGEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127045141 12704514 1 Chronic obstructive pulmonary disease
127045141 12704514 2 Chronic obstructive pulmonary disease
127045141 12704514 3 Product used for unknown indication
127045141 12704514 5 Diuretic therapy
127045141 12704514 6 Insomnia
127045141 12704514 7 Hypercholesterolaemia
127045141 12704514 8 Insomnia
127045141 12704514 9 Product used for unknown indication
127045141 12704514 10 Anxiolytic therapy
127045141 12704514 11 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127045141 12704514 OT
127045141 12704514 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127045141 12704514 Arterial occlusive disease
127045141 12704514 Atrial fibrillation
127045141 12704514 Atrioventricular block
127045141 12704514 Bedridden
127045141 12704514 Blood urine present
127045141 12704514 Cardiac failure
127045141 12704514 Cardiac murmur
127045141 12704514 Catheter placement
127045141 12704514 Chronic obstructive pulmonary disease
127045141 12704514 Condition aggravated
127045141 12704514 Emphysema
127045141 12704514 Haemorrhage
127045141 12704514 Hypotension
127045141 12704514 Palliative care
127045141 12704514 Product use issue
127045141 12704514 Pulmonary oedema
127045141 12704514 Respiratory failure

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
127045141 12704514 7 20160803 0