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
110834962 11083496 2 F 20160913 20150501 20160922 EXP US-BAYER-2015-153962 BAYER 0.00 A M Y 0.00000 20160922 OT 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
110834962 11083496 1 PS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 UNK 21085 FILM-COATED TABLET
110834962 11083496 2 SS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 500 MG, UNK 21085 500 MG FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110834962 11083496 1 Pneumonia
110834962 11083496 2 Pneumonia

Outcome of event

Event ID CASEID OUTC COD
110834962 11083496 DS
110834962 11083496 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
110834962 11083496 Activities of daily living impaired
110834962 11083496 Anxiety
110834962 11083496 Discomfort
110834962 11083496 Eye injury
110834962 11083496 Eye irritation
110834962 11083496 Eye pain
110834962 11083496 Feeling of despair
110834962 11083496 Headache
110834962 11083496 Impaired driving ability
110834962 11083496 Iridocyclitis
110834962 11083496 Lacrimation increased
110834962 11083496 Mood altered
110834962 11083496 Mydriasis
110834962 11083496 Ocular discomfort
110834962 11083496 Pain
110834962 11083496 Photophobia
110834962 11083496 Pigment dispersion syndrome
110834962 11083496 Sudden visual loss
110834962 11083496 Uveitis
110834962 11083496 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
110834962 11083496 1 201303 0
110834962 11083496 2 20130709 0