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
126281251 12628125 1 I 20150425 20160726 20160808 20160808 EXP CN-DEXPHARM-20161664 DEXCEL YU, M.; QIAN, J.; GUO, D.; LI, L.; LIU, X. SEVERE ADVERSE REACTIONS CAUSED BY OMEPRAZOLE: A CASE REPORT. EXPERIMENTAL AND THERAPEUTIC MEDICINE 2016, V12, P1103-1106 61.00 YR A F Y 0.00000 20160807 OT CN CN

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
126281251 12628125 1 PS OMEPRAZOLE. OMEPRAZOLE 1 Oral DAILY DOSE: 40 MG MILLGRAM(S) EVERY DAYS U U 0 20 MG TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126281251 12628125 1 Abdominal discomfort

Outcome of event

Event ID CASEID OUTC COD
126281251 12628125 OT
126281251 12628125 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126281251 12628125 Acute kidney injury
126281251 12628125 Anaphylactic shock
126281251 12628125 Diarrhoea
126281251 12628125 Electrolyte imbalance
126281251 12628125 Metabolic acidosis
126281251 12628125 Nausea
126281251 12628125 Rash
126281251 12628125 Vomiting

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

no results found

Therapies reported

no results found