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
126876491 12687649 1 I 20160818 20160826 20160826 EXP KR-ASTRAZENECA-2016SE89022 ASTRAZENECA 45.00 YR M Y 0.00000 20160826 MD KR KR

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
126876491 12687649 1 PS ESOMEPRAZOLE ESOMEPRAZOLE 1 Intravenous (not otherwise specified) Y U 21689 INTRAVENOUS INFUSION
126876491 12687649 2 C SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 160/4.5 MCG 0
126876491 12687649 3 C ASPIRIN. ASPIRIN 1 0 100 MG QD
126876491 12687649 4 C CLOPIDOGREL CLOPIDOGREL BISULFATE 1 0 75 MG QD
126876491 12687649 5 C ATORVASTATIN ATORVASTATIN 1 0 10 MG QD
126876491 12687649 6 C CANDESARTAN CANDESARTAN 1 0 8 MG QD
126876491 12687649 7 C INSULIN INSULIN NOS 1 Intravenous (not otherwise specified) 0
126876491 12687649 8 C SALINE SODIUM CHLORIDE 1 0
126876491 12687649 9 C LACTULOSE. LACTULOSE 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126876491 12687649 1 Gastrooesophageal reflux disease
126876491 12687649 2 Asthma
126876491 12687649 9 Constipation

Outcome of event

Event ID CASEID OUTC COD
126876491 12687649 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126876491 12687649 Rhabdomyolysis

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

no results found

Therapies reported

no results found