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
73291442 7329144 2 F 20090622 0 20100305 20131231 EXP 2010S1001231 CB FLEET 81.00 YR F N 0.00000 0 LW 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
73291442 7329144 1 PS FLEET PHOSPHO-SODA 1 90 ML; TOTAL; PO D D 0
73291442 7329144 3 SS MOBIC 1 20998
73291442 7329144 5 C ELAVIL (AMITRIPTYLINE HYDROCHLORIDE) 1 0
73291442 7329144 7 C PREVACID (LANSOPRAZOLE) 1 0
73291442 7329144 9 C COVERA (VERAPAMIL HYDROCHLORIDE) 2 0
73291442 7329144 11 C TYLENOL (PARACETAMOL) 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
73291442 7329144 1 Colonoscopy

Outcome of event

Event ID CASEID OUTC COD
73291442 7329144 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
73291442 7329144 Hyperparathyroidism
73291442 7329144 Hyponatraemia
73291442 7329144 Hypotension
73291442 7329144 Nephrogenic anaemia
73291442 7329144 Renal failure acute
73291442 7329144 Renal failure chronic
73291442 7329144 Renal tubular necrosis

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
73291442 7329144 3 20030726 0