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
110203282 11020328 2 F 20160609 20150413 20160708 PER US-ASTRAZENECA-2015SE31135 ASTRAZENECA 73.00 YR F Y 86.20000 KG 20160708 OT 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
110203282 11020328 1 PS NEXIUM 24HR ESOMEPRAZOLE MAGNESIUM 1 Oral UNK U 204655
110203282 11020328 2 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral TAKE MORE THAN ONE U 0
110203282 11020328 3 SS POTASSIUM POTASSIUM 1 Unknown U U 0 80 MEQ QD
110203282 11020328 4 SS RANITIDINE. RANITIDINE 1 Unknown 3-4 TABLETS U U 0 TABLET
110203282 11020328 5 C LISINOPRIL. LISINOPRIL 1 Unknown 0 20 MG QD
110203282 11020328 6 C AMLODIPINE AMLODIPINE BESYLATE 1 0 10 MG QD
110203282 11020328 7 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 0
110203282 11020328 8 C PROTONIX PANTOPRAZOLE SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110203282 11020328 3 Cardiac disorder
110203282 11020328 4 Gastrooesophageal reflux disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
110203282 11020328 Burn oesophageal
110203282 11020328 Dizziness
110203282 11020328 Gastrooesophageal reflux disease
110203282 11020328 Hypokalaemia

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

no results found

Therapies reported

no results found