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
125801001 12580100 1 I 201601 20160708 20160721 20160721 EXP DE-BFARM-16231183 DE-TEVA-675807GER TEVA 29.00 YR M Y 82.00000 KG 20160721 CN DE DE

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
125801001 12580100 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral Y 74124
125801001 12580100 2 SS LEVOFLOXACIN. LEVOFLOXACIN 1 Oral U 76361

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125801001 12580100 1 Bladder discomfort
125801001 12580100 2 Bladder discomfort

Outcome of event

Event ID CASEID OUTC COD
125801001 12580100 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125801001 12580100 Anxiety
125801001 12580100 Arthralgia
125801001 12580100 Cardiovascular disorder
125801001 12580100 Chills
125801001 12580100 Dizziness
125801001 12580100 Feeling cold
125801001 12580100 Gait disturbance
125801001 12580100 Hot flush
125801001 12580100 Joint crepitation
125801001 12580100 Myalgia
125801001 12580100 Palpitations
125801001 12580100 Photophobia
125801001 12580100 Rash
125801001 12580100 Retching
125801001 12580100 Tendonitis
125801001 12580100 Visual impairment
125801001 12580100 Vomiting

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
125801001 12580100 1 201601 0
125801001 12580100 2 201601 0