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
116169962 11616996 2 F 2016 20160721 20151009 20160803 PER US-BAYER-2015-435174 BAYER 0.00 F Y 58.96000 KG 20160803 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
116169962 11616996 1 PS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 400 MG, UNK 21085 400 MG FILM-COATED TABLET
116169962 11616996 2 SS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 400 MG, UNK 21085 400 MG FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116169962 11616996 1 Sinusitis
116169962 11616996 2 Sinusitis

Outcome of event

Event ID CASEID OUTC COD
116169962 11616996 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116169962 11616996 Anhedonia
116169962 11616996 Anxiety
116169962 11616996 Emotional distress
116169962 11616996 Injury
116169962 11616996 Neuropathy peripheral
116169962 11616996 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
116169962 11616996 1 20090415 20090425 0
116169962 11616996 2 20100518 20100528 0