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
125671471 12567147 1 I 201601 20160708 20160718 20160718 EXP DE-BFARM-16231183 DE-MYLANLABS-2016M1028730 MYLAN 0.00 Y 0.00000 20160718 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
125671471 12567147 1 PS LEVOFLOXACIN. LEVOFLOXACIN 1 Oral UNK U U 76276
125671471 12567147 2 SS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral UNK Y U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125671471 12567147 1 Bladder discomfort
125671471 12567147 2 Bladder discomfort

Outcome of event

Event ID CASEID OUTC COD
125671471 12567147 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125671471 12567147 Anxiety
125671471 12567147 Arthralgia
125671471 12567147 Cardiovascular disorder
125671471 12567147 Chills
125671471 12567147 Dizziness
125671471 12567147 Feeling cold
125671471 12567147 Gait disturbance
125671471 12567147 Hot flush
125671471 12567147 Joint crepitation
125671471 12567147 Myalgia
125671471 12567147 Palpitations
125671471 12567147 Photophobia
125671471 12567147 Rash
125671471 12567147 Retching
125671471 12567147 Tendonitis
125671471 12567147 Visual impairment
125671471 12567147 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
125671471 12567147 1 201601 0
125671471 12567147 2 201601 0