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
125315771 12531577 1 I 2012 20160623 20160706 20160706 EXP DE-BFARM-16211860 DE-BAYER-2016-127096 BAYER 50.00 YR A F Y 96.00000 KG 20160706 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
125315771 12531577 1 SS NORFLOXACIN NORFLOXACIN 1 Oral 400 MG, UNK 0 400 MG FILM-COATED TABLET
125315771 12531577 2 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral UNK 19537
125315771 12531577 3 SS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral UNK 19537

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125315771 12531577 1 Cystitis
125315771 12531577 2 Cystitis
125315771 12531577 3 Cystitis

Outcome of event

Event ID CASEID OUTC COD
125315771 12531577 HO
125315771 12531577 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125315771 12531577 Abdominal pain upper
125315771 12531577 Anxiety
125315771 12531577 Arthralgia
125315771 12531577 Blood pressure increased
125315771 12531577 Disturbance in attention
125315771 12531577 Dizziness
125315771 12531577 Dyspnoea
125315771 12531577 Facial paralysis
125315771 12531577 Fatigue
125315771 12531577 Hypoaesthesia
125315771 12531577 Muscular weakness
125315771 12531577 Nausea
125315771 12531577 Panic attack
125315771 12531577 Presyncope
125315771 12531577 Tinnitus
125315771 12531577 Tremor
125315771 12531577 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
125315771 12531577 1 20120710 0
125315771 12531577 2 20140622 0
125315771 12531577 3 20160617 0