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
93423884 9342388 4 F 201304 20160721 20130611 20160801 PER US-BAYER-2013-069442 BAYER 31.46 YR F Y 53.97000 KG 20160801 CN 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
93423884 9342388 1 PS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 Oral DAILY DOSE 400 MG 21085 400 MG FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
93423884 9342388 1 Sinusitis

Outcome of event

Event ID CASEID OUTC COD
93423884 9342388 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
93423884 9342388 Activities of daily living impaired
93423884 9342388 Anxiety
93423884 9342388 Asthenia
93423884 9342388 Depressed level of consciousness
93423884 9342388 Disturbance in attention
93423884 9342388 Dyspepsia
93423884 9342388 Dysstasia
93423884 9342388 Emotional distress
93423884 9342388 Fear
93423884 9342388 Gait disturbance
93423884 9342388 Insomnia
93423884 9342388 Multiple injuries
93423884 9342388 Muscle spasms
93423884 9342388 Muscle tightness
93423884 9342388 Neuropathy peripheral
93423884 9342388 Pain
93423884 9342388 Pain in extremity
93423884 9342388 Paraesthesia
93423884 9342388 Quality of life decreased
93423884 9342388 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
93423884 9342388 1 20130425 20130428 0