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
92603004 9260300 4 F 20160915 20130429 20160927 EXP US-BAYER-2013-052605 BAYER 61.00 YR A F Y 0.00000 20160927 MD US 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
92603004 9260300 1 PS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 400 MG, UNK Y 21085 400 MG FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
92603004 9260300 1 Sinusitis

Outcome of event

Event ID CASEID OUTC COD
92603004 9260300 OT
92603004 9260300 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
92603004 9260300 Anhedonia
92603004 9260300 Emotional distress
92603004 9260300 Injury
92603004 9260300 Intraocular pressure test
92603004 9260300 Iris hypopigmentation
92603004 9260300 Pain
92603004 9260300 Photophobia
92603004 9260300 Pigment dispersion syndrome
92603004 9260300 Pigmentary glaucoma
92603004 9260300 Presbyopia
92603004 9260300 Quality of life decreased
92603004 9260300 Somatic symptom disorder
92603004 9260300 Uveitis
92603004 9260300 Visual impairment

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
92603004 9260300 1 20111229 20120103 0