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
116173012 11617301 2 F 20160804 20151009 20160816 PER US-BAYER-2015-437091 BAYER 0.00 F Y 42.18000 KG 20160816 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
116173012 11617301 1 PS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 UNK 21085 FILM-COATED TABLET
116173012 11617301 2 SS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 UNK 21085 FILM-COATED TABLET
116173012 11617301 3 SS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 UNK 21085 FILM-COATED TABLET
116173012 11617301 4 SS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 UNK 21085 FILM-COATED TABLET
116173012 11617301 5 SS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 500 MG, UNK 0 500 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116173012 11617301 1 Sinusitis
116173012 11617301 2 Ear infection
116173012 11617301 3 Sinusitis
116173012 11617301 4 Sinusitis
116173012 11617301 5 Blood urine present

Outcome of event

Event ID CASEID OUTC COD
116173012 11617301 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116173012 11617301 Anxiety
116173012 11617301 Emotional distress
116173012 11617301 Injury
116173012 11617301 Neuropathy peripheral
116173012 11617301 Pain

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
116173012 11617301 1 20010315 0
116173012 11617301 2 20010917 0
116173012 11617301 3 20020416 0
116173012 11617301 4 200410 0