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
126392281 12639228 1 I 2013 20160614 20160810 20160810 PER US-ASTRAZENECA-2016SE66209 ASTRAZENECA 62.00 YR F Y 59.00000 KG 20160810 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
126392281 12639228 1 PS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral Y U 0
126392281 12639228 2 SS LANSOPRAZOLE. LANSOPRAZOLE 1 Oral UNK 0 30 MG CAPSULE QD
126392281 12639228 3 SS UNKNOWN MEDICATION UNSPECIFIED INGREDIENT 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126392281 12639228 1 Gastrooesophageal reflux disease
126392281 12639228 2 Gastrooesophageal reflux disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126392281 12639228 Ankle fracture
126392281 12639228 Blood sodium decreased
126392281 12639228 Diarrhoea
126392281 12639228 Dyspepsia
126392281 12639228 Dysstasia
126392281 12639228 Feeling abnormal
126392281 12639228 Pollakiuria
126392281 12639228 Somnolence

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

no results found

Therapies reported

no results found