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
82479256 8247925 6 F 20160921 20111116 20160929 EXP US-ASTRAZENECA-2011SE68115 ASTRAZENECA 0.00 M Y 0.00000 20160929 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
82479256 8247925 1 PS CRESTOR ROSUVASTATIN CALCIUM 1 Oral U 21366 10 MG TABLET QD
82479256 8247925 2 C PROTONIX PANTOPRAZOLE SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
82479256 8247925 2 Gastrooesophageal reflux disease

Outcome of event

Event ID CASEID OUTC COD
82479256 8247925 HO
82479256 8247925 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
82479256 8247925 Arterial occlusive disease
82479256 8247925 Arthritis reactive
82479256 8247925 Blood cholesterol increased
82479256 8247925 Gastrointestinal disorder
82479256 8247925 Glucose tolerance impaired
82479256 8247925 Haematemesis
82479256 8247925 Hypertension
82479256 8247925 Malaise
82479256 8247925 Myalgia
82479256 8247925 Pancreatic carcinoma
82479256 8247925 Pancreatitis
82479256 8247925 Pseudocyst
82479256 8247925 Rash
82479256 8247925 Thyroid disorder

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found