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
116169542 11616954 2 F 200804 20160803 20151009 20160815 PER US-BAYER-2015-434781 BAYER 54.31 YR M Y 103.40000 KG 20160815 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
116169542 11616954 1 PS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 400 MG, QD 21085 400 MG FILM-COATED TABLET QD
116169542 11616954 2 SS CIPROFLOXACIN. CIPROFLOXACIN 1 UNK 0 500 MG
116169542 11616954 3 C LEVAQUIN LEVOFLOXACIN 1 DAILY DOSE 500 MG 0 500 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116169542 11616954 1 Bronchitis
116169542 11616954 2 Respiratory tract infection
116169542 11616954 3 Respiratory tract infection

Outcome of event

Event ID CASEID OUTC COD
116169542 11616954 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116169542 11616954 Anxiety
116169542 11616954 Emotional distress
116169542 11616954 Injury
116169542 11616954 Neuropathy peripheral
116169542 11616954 Pain
116169542 11616954 Quality of life decreased

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
116169542 11616954 1 20080426 20080428 0
116169542 11616954 2 20070424 0
116169542 11616954 3 200803 0