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
104418507 10441850 7 F 201403 20160908 20140909 20160912 EXP US-GLAXOSMITHKLINE-A1048693A GLAXOSMITHKLINE 79.67 YR F Y 0.00000 20160912 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
104418507 10441850 1 PS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), BID Y 2ZP8461 21077 1 DF INHALATION POWDER BID
104418507 10441850 2 SS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 U 0
104418507 10441850 3 SS COREG CARVEDILOL 1 Oral 25 MG TABLET. 012005212 0 25 MG TABLET BID
104418507 10441850 4 SS COREG CARVEDILOL 1 UNK UNKNOWN 0 TABLET
104418507 10441850 5 SS COREG CARVEDILOL 1 Unknown 12.5 MG, U 0 12.5 MG TABLET
104418507 10441850 6 SS FUROSEMIDE. FUROSEMIDE 1 Unknown 0
104418507 10441850 7 SS Morphine MORPHINE 1 Unknown U 0
104418507 10441850 8 SS COUMADIN WARFARIN SODIUM 1 Unknown Y UNKNOWN 0 TABLET
104418507 10441850 9 SS CARVEDILOL. CARVEDILOL 1 U 0
104418507 10441850 10 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 0
104418507 10441850 11 C XOPENEX LEVALBUTEROL HYDROCHLORIDE 1 0
104418507 10441850 12 C POTASSIUM CHLORIDE. POTASSIUM CHLORIDE 1 0
104418507 10441850 13 C OMEPRAZOLE. OMEPRAZOLE 1 0
104418507 10441850 14 C COZAAR LOSARTAN POTASSIUM 1 0
104418507 10441850 15 C NEURONTIN GABAPENTIN 1 0
104418507 10441850 16 C LIPITOR ATORVASTATIN CALCIUM 1 0
104418507 10441850 17 C LANTUS INSULIN GLARGINE 1 0
104418507 10441850 18 C NOVOLOG INSULIN ASPART 1 0
104418507 10441850 19 C Baby aspirin ASPIRIN 1 0
104418507 10441850 20 C TYLENOL ARTHRITIS PAIN ACETAMINOPHEN 1 0
104418507 10441850 21 C TRAMADOL HCL TRAMADOL HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104418507 10441850 1 Chronic obstructive pulmonary disease
104418507 10441850 2 Chronic obstructive pulmonary disease
104418507 10441850 3 Cardiac disorder
104418507 10441850 6 Product used for unknown indication
104418507 10441850 7 Pain
104418507 10441850 8 Cardiac ventricular thrombosis

Outcome of event

Event ID CASEID OUTC COD
104418507 10441850 OT
104418507 10441850 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
104418507 10441850 Adverse event
104418507 10441850 Amnesia
104418507 10441850 Asthenia
104418507 10441850 Atrial fibrillation
104418507 10441850 Cardiac ventricular thrombosis
104418507 10441850 Cerebrovascular accident
104418507 10441850 Contusion
104418507 10441850 Drug hypersensitivity
104418507 10441850 Drug ineffective
104418507 10441850 Dysarthria
104418507 10441850 Dysgraphia
104418507 10441850 Dysphonia
104418507 10441850 Extremity necrosis
104418507 10441850 Haemorrhage
104418507 10441850 Hospitalisation
104418507 10441850 Ill-defined disorder
104418507 10441850 Infection
104418507 10441850 Joint crepitation
104418507 10441850 Lung disorder
104418507 10441850 Malaise
104418507 10441850 Memory impairment
104418507 10441850 Micturition urgency
104418507 10441850 Musculoskeletal disorder
104418507 10441850 Neuropathy peripheral
104418507 10441850 Oxygen saturation decreased
104418507 10441850 Pain in extremity
104418507 10441850 Peripheral swelling
104418507 10441850 Surgery
104418507 10441850 Swelling face
104418507 10441850 Toxicity to various agents
104418507 10441850 Transient ischaemic attack
104418507 10441850 Tremor

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
104418507 10441850 3 2005 0
104418507 10441850 4 20081204 0