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
125825211 12582521 1 I 201601 20160708 20160722 20160722 EXP DE-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-120704 RANBAXY 29.00 YR M Y 82.00000 KG 20160722 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
125825211 12582521 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral UNK N U 75747
125825211 12582521 2 SS LEVOFLOXACIN. LEVOFLOXACIN 1 Oral UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125825211 12582521 1 Bladder discomfort
125825211 12582521 2 Bladder discomfort

Outcome of event

Event ID CASEID OUTC COD
125825211 12582521 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125825211 12582521 Anxiety
125825211 12582521 Arthralgia
125825211 12582521 Cardiovascular disorder
125825211 12582521 Chills
125825211 12582521 Dizziness
125825211 12582521 Feeling cold
125825211 12582521 Gait disturbance
125825211 12582521 Hot flush
125825211 12582521 Joint crepitation
125825211 12582521 Myalgia
125825211 12582521 Palpitations
125825211 12582521 Photophobia
125825211 12582521 Rash
125825211 12582521 Retching
125825211 12582521 Tendonitis
125825211 12582521 Visual impairment
125825211 12582521 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
125825211 12582521 1 201601 0
125825211 12582521 2 201601 0