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
125396161 12539616 1 I 2012 20160623 20160708 20160708 EXP DE-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-119845 RANBAXY 50.00 YR F Y 96.00000 KG 20160708 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
125396161 12539616 1 SS Norfloxacin NORFLOXACIN 1 Oral UNK U U 0
125396161 12539616 2 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral UNK U U 75747
125396161 12539616 3 SS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral UNK U U 75747

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125396161 12539616 1 Cystitis
125396161 12539616 2 Cystitis
125396161 12539616 3 Cystitis

Outcome of event

Event ID CASEID OUTC COD
125396161 12539616 OT
125396161 12539616 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125396161 12539616 Abdominal pain upper
125396161 12539616 Anxiety
125396161 12539616 Arthralgia
125396161 12539616 Blood pressure increased
125396161 12539616 Disturbance in attention
125396161 12539616 Dizziness
125396161 12539616 Dyspnoea
125396161 12539616 Facial paralysis
125396161 12539616 Fatigue
125396161 12539616 Hypoaesthesia
125396161 12539616 Muscular weakness
125396161 12539616 Nausea
125396161 12539616 Panic attack
125396161 12539616 Presyncope
125396161 12539616 Tinnitus
125396161 12539616 Tremor
125396161 12539616 Visual impairment

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
125396161 12539616 1 20120710 0
125396161 12539616 2 20140622 0
125396161 12539616 3 20160617 0