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
126244951 12624495 1 I 20151205 0 20160804 20160804 DIR 64.00 YR F N 209.00000 LBS 0 N 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
126244951 12624495 1 PS FENOFIBRATE. FENOFIBRATE 1 Y 0
126244951 12624495 3 C TRILIPIX FENOFIBRIC ACID 1 0
126244951 12624495 5 C LISINOPRIL. LISINOPRIL 1 0
126244951 12624495 7 C FLUOXETINE FLUOXETINE HYDROCHLORIDE 1 0
126244951 12624495 9 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 0
126244951 12624495 11 C GLIPIZIDE. GLIPIZIDE 1 0
126244951 12624495 13 C ASPRIN ASPIRIN 1 0
126244951 12624495 15 C VITAMIN D CHOLECALCIFEROL 1 0
126244951 12624495 16 C TUMS CALCIUM CARBONATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126244951 12624495 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126244951 12624495 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126244951 12624495 Abdominal discomfort
126244951 12624495 Abdominal distension
126244951 12624495 Abdominal pain upper
126244951 12624495 Confusional state
126244951 12624495 Dizziness
126244951 12624495 Flatulence
126244951 12624495 Gastric haemorrhage
126244951 12624495 Nausea

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

no results found

Therapies reported

no results found