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
125754511 12575451 1 I 201601 20160708 20160720 20160720 EXP DE-BFARM-16231183 DE-BAYER-2016-137848 BAYER 29.00 YR A M Y 82.00000 KG 20160720 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
125754511 12575451 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral UNK 19537
125754511 12575451 2 SS LEVOFLOXACIN. LEVOFLOXACIN 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125754511 12575451 1 Bladder discomfort
125754511 12575451 2 Bladder discomfort

Outcome of event

Event ID CASEID OUTC COD
125754511 12575451 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125754511 12575451 Anxiety
125754511 12575451 Arthralgia
125754511 12575451 Cardiovascular disorder
125754511 12575451 Chills
125754511 12575451 Dizziness
125754511 12575451 Feeling cold
125754511 12575451 Gait disturbance
125754511 12575451 Hot flush
125754511 12575451 Joint crepitation
125754511 12575451 Myalgia
125754511 12575451 Palpitations
125754511 12575451 Photophobia
125754511 12575451 Rash
125754511 12575451 Retching
125754511 12575451 Tendonitis
125754511 12575451 Visual impairment
125754511 12575451 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
125754511 12575451 1 201601 0
125754511 12575451 2 201601 0