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
126174241 12617424 1 I 20160611 0 20160802 20160802 DIR 89.00 YR M N 150.00000 LBS 20160731 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
126174241 12617424 1 PS LEVOFLOXACIN. LEVOFLOXACIN 1 Oral 1 TABLET DAILY IV X 2 DAYS IN HOSPITAL BY MOUTH X 5 DAYS N D 20170607 0 1 DF COATED TABLET QD
126174241 12617424 2 C AMLODIPINE AMLODIPINE BESYLATE 1 0
126174241 12617424 3 C PRAVASTATIN. PRAVASTATIN 1 0
126174241 12617424 4 C TERAZOSIN TERAZOSINTERAZOSIN HYDROCHLORIDE 1 0
126174241 12617424 5 C CALCITRIOL. CALCITRIOL 1 0
126174241 12617424 6 C FISH OIL FISH OIL 1 0
126174241 12617424 7 C VITAMIN B12 CYANOCOBALAMIN 1 0
126174241 12617424 8 C B COMPLEX VITAMIN 2 0
126174241 12617424 9 C PRESERVISION MINERALSVITAMINS 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126174241 12617424 1 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
126174241 12617424 DS
126174241 12617424 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126174241 12617424 Depression
126174241 12617424 Immobile
126174241 12617424 Pain
126174241 12617424 Swelling
126174241 12617424 Tendon rupture
126174241 12617424 Tendonitis

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
126174241 12617424 1 20160606 20160612 0