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
125544971 12554497 1 I 201601 20160708 20160713 20160713 EXP GXKR2016DE003220 SANDOZ 0.00 Y 0.00000 20160713 OT 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
125544971 12554497 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral UNK MG, UNK Y U 76593
125544971 12554497 2 SS LEVOFLOXACIN. LEVOFLOXACIN 1 Oral UNK UKN, UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125544971 12554497 1 Bladder discomfort
125544971 12554497 2 Bladder discomfort

Outcome of event

Event ID CASEID OUTC COD
125544971 12554497 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125544971 12554497 Anxiety
125544971 12554497 Arthralgia
125544971 12554497 Cardiovascular disorder
125544971 12554497 Chills
125544971 12554497 Dizziness
125544971 12554497 Feeling cold
125544971 12554497 Gait disturbance
125544971 12554497 Hot flush
125544971 12554497 Joint crepitation
125544971 12554497 Myalgia
125544971 12554497 Palpitations
125544971 12554497 Photophobia
125544971 12554497 Rash
125544971 12554497 Retching
125544971 12554497 Tendonitis
125544971 12554497 Visual impairment
125544971 12554497 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
125544971 12554497 1 201601 0
125544971 12554497 2 201601 0