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
127769391 12776939 1 I 1994 20160916 20160923 20160923 EXP US-ASTRAZENECA-2016SF00227 ASTRAZENECA 43.00 YR F Y 52.40000 KG 20160923 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
127769391 12776939 1 PS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral U 21153 20 MG BID
127769391 12776939 2 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral U 21153 40 MG BID
127769391 12776939 3 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral GENERIC U 21153
127769391 12776939 4 SS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral U 0
127769391 12776939 5 C LAMOTRIGINE. LAMOTRIGINE 1 Oral 0 100 MG Q12H
127769391 12776939 6 C CLONIDINE HCL CLONIDINE HYDROCHLORIDE 1 Oral 0.1MG UNKNOWN 0 .1 MG
127769391 12776939 7 C XOLAIR OMALIZUMAB 1 0
127769391 12776939 8 C XOLAIR OMALIZUMAB 1 0
127769391 12776939 9 C BONIVA IBANDRONATE SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127769391 12776939 1 Gastrooesophageal reflux disease
127769391 12776939 2 Gastrooesophageal reflux disease
127769391 12776939 3 Gastrooesophageal reflux disease
127769391 12776939 4 Gastrooesophageal reflux disease
127769391 12776939 5 Tremor
127769391 12776939 6 Blood pressure abnormal
127769391 12776939 7 Multiple allergies
127769391 12776939 8 Asthma
127769391 12776939 9 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
127769391 12776939 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127769391 12776939 Abdominal discomfort
127769391 12776939 Abdominal distension
127769391 12776939 Abdominal pain upper
127769391 12776939 Acute sinusitis
127769391 12776939 Alopecia
127769391 12776939 Amnesia
127769391 12776939 Anxiety
127769391 12776939 Asthma
127769391 12776939 Blood magnesium decreased
127769391 12776939 Bowel movement irregularity
127769391 12776939 Calcium deficiency
127769391 12776939 Chronic fatigue syndrome
127769391 12776939 Clostridium difficile infection
127769391 12776939 Colitis ischaemic
127769391 12776939 Dehydration
127769391 12776939 Depression
127769391 12776939 Diarrhoea
127769391 12776939 Dizziness
127769391 12776939 Drug ineffective
127769391 12776939 Dyspepsia
127769391 12776939 Dysphagia
127769391 12776939 Erythema
127769391 12776939 Eye disorder
127769391 12776939 Facial bones fracture
127769391 12776939 Fall
127769391 12776939 Fibromyalgia
127769391 12776939 Flatulence
127769391 12776939 Fluid retention
127769391 12776939 Fungal infection
127769391 12776939 Gastrointestinal inflammation
127769391 12776939 Headache
127769391 12776939 Hypersensitivity
127769391 12776939 Hypertension
127769391 12776939 Influenza like illness
127769391 12776939 Muscular weakness
127769391 12776939 Myalgia
127769391 12776939 Nausea
127769391 12776939 Off label use
127769391 12776939 Osteoporosis
127769391 12776939 Palpitations
127769391 12776939 Photosensitivity reaction
127769391 12776939 Product use issue
127769391 12776939 Pruritus
127769391 12776939 Rhinitis
127769391 12776939 Sinus congestion
127769391 12776939 Tremor
127769391 12776939 Vision blurred
127769391 12776939 Vitamin B12 decreased

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
127769391 12776939 1 2001 2001 0
127769391 12776939 2 2001 20160915 0