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
126708311 12670831 1 I 20160719 0 20160819 20160819 DIR 61.00 YR F N 140.00000 LBS 20160709 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
126708311 12670831 1 PS LEVAQUIN LEVOFLOXACIN 1 Oral 500 MG 10 TAB 1-TAB ONCE A DAY BY MOUTH N D 65862-0537-50 20170719 0 500 MG COATED TABLET QD
126708311 12670831 3 C LOSARTAN POTASSIUM. LOSARTAN POTASSIUM 1 0
126708311 12670831 4 C SPIRONOLACTONE. SPIRONOLACTONE 1 0
126708311 12670831 6 C COD LIVER OIL COD LIVER OIL 1 0
126708311 12670831 8 C CINNAMON. CINNAMON 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126708311 12670831 1 Sinusitis
126708311 12670831 1 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
126708311 12670831 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126708311 12670831 Arthralgia
126708311 12670831 Gait disturbance
126708311 12670831 Swelling
126708311 12670831 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
126708311 12670831 1 20160714 20160719 0