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
127510211 12751021 1 I 20090714 20091104 20160915 20160915 EXP PHHO2009US13678 NOVARTIS 56.08 YR F Y 113.40000 KG 20160915 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
127510211 12751021 1 PS LOTREL AMLODIPINE BESYLATEBENAZEPRIL HYDROCHLORIDE 1 Oral UNK 20364
127510211 12751021 2 SS CELECOXIB. CELECOXIB 1 Oral 200 MG, UNK Y 0 200 MG
127510211 12751021 3 SS IBUPROFEN. IBUPROFEN 1 Oral 200 MG, UNK Y 0 200 MG
127510211 12751021 4 SS NAPROXEN. NAPROXEN 1 Oral 200 MG, UNK Y 0 200 MG TABLET
127510211 12751021 5 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Unknown UNK Y 0
127510211 12751021 6 C KLOR-CON POTASSIUM CHLORIDE 1 Oral UNK 0
127510211 12751021 7 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 Oral 0
127510211 12751021 8 C DIAZEPAM. DIAZEPAM 1 Oral U 0
127510211 12751021 9 C FUROSEMIDE. FUROSEMIDE 1 Oral U 0
127510211 12751021 10 C CYCLOBENZAPRINE CYCLOBENZAPRINE 1 Oral U 0
127510211 12751021 11 C ZANTAC RANITIDINE HYDROCHLORIDE 1 Oral UNK 0
127510211 12751021 12 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) U 0
127510211 12751021 13 C ALBUTEROL. ALBUTEROL 1 Respiratory (inhalation) U 0
127510211 12751021 14 C FLONASE FLUTICASONE PROPIONATE 1 Oral U 0
127510211 12751021 15 C PAROXETINE HYDROCHLORIDE. PAROXETINE HYDROCHLORIDE 1 Oral U 0
127510211 12751021 16 C BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 Oral UNK MG, UNK U 0
127510211 12751021 17 C GAS-X DIMETHICONE 1 Oral U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127510211 12751021 1 Hypertension
127510211 12751021 2 Arthritis
127510211 12751021 3 Arthritis
127510211 12751021 4 Arthritis
127510211 12751021 5 Product used for unknown indication
127510211 12751021 6 Product used for unknown indication
127510211 12751021 7 Product used for unknown indication
127510211 12751021 8 Product used for unknown indication
127510211 12751021 9 Product used for unknown indication
127510211 12751021 10 Product used for unknown indication
127510211 12751021 11 Product used for unknown indication
127510211 12751021 12 Product used for unknown indication
127510211 12751021 13 Product used for unknown indication
127510211 12751021 14 Product used for unknown indication
127510211 12751021 15 Product used for unknown indication
127510211 12751021 16 Product used for unknown indication
127510211 12751021 17 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127510211 12751021 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127510211 12751021 Dysphagia
127510211 12751021 Face oedema
127510211 12751021 Hypersensitivity
127510211 12751021 Hypertension

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
127510211 12751021 1 2007 20090715 0
127510211 12751021 2 20090111 20120801 0
127510211 12751021 3 20090111 20120801 0
127510211 12751021 4 20090111 20120801 0
127510211 12751021 5 20090110 20090714 0
127510211 12751021 6 20090310 0
127510211 12751021 7 200903 0
127510211 12751021 8 2000 0
127510211 12751021 9 2007 0
127510211 12751021 10 1995 0
127510211 12751021 11 2008 0
127510211 12751021 12 2003 0
127510211 12751021 13 1992 0
127510211 12751021 14 2000 0
127510211 12751021 15 20090310 0
127510211 12751021 16 20090429 0
127510211 12751021 17 20090202 0