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
116170023 11617002 3 F 20160721 20151009 20160804 PER US-BAYER-2015-435141 BAYER 0.00 A M Y 92.97000 KG 20160804 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
116170023 11617002 1 PS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 400 MG, UNK 21085 400 MG FILM-COATED TABLET
116170023 11617002 2 SS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 400 MG, UNK 21085 400 MG FILM-COATED TABLET
116170023 11617002 3 SS CIPROFLOXACIN. CIPROFLOXACIN 1 0.3 %, UNK 0 .3 PCT MODIFIED-RELEASE FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116170023 11617002 1 Sinusitis
116170023 11617002 2 Sinusitis

Outcome of event

Event ID CASEID OUTC COD
116170023 11617002 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116170023 11617002 Anxiety
116170023 11617002 Cardiovascular disorder
116170023 11617002 Depression
116170023 11617002 Emotional distress
116170023 11617002 Injury
116170023 11617002 Mental disorder
116170023 11617002 Musculoskeletal injury
116170023 11617002 Nervous system disorder
116170023 11617002 Neuropathy peripheral
116170023 11617002 Pain
116170023 11617002 Post-traumatic stress disorder
116170023 11617002 Skin injury

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
116170023 11617002 1 20050701 20050720 0
116170023 11617002 2 20050807 0
116170023 11617002 3 20050909 0