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
125277451 12527745 1 I 2012 20160623 20160705 20160705 EXP DE-CADRBFARM-2016012913 DE-DRREDDYS-GER/GER/16/0080981 DR REDDYS 50.00 YR F Y 96.00000 KG 20160705 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
125277451 12527745 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral U U UNKNOWN 75593
125277451 12527745 2 SS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral U U UNKNOWN 75593
125277451 12527745 3 SS Norfloxacin NORFLOXACIN 1 Oral U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125277451 12527745 1 Cystitis
125277451 12527745 3 Cystitis

Outcome of event

Event ID CASEID OUTC COD
125277451 12527745 HO
125277451 12527745 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125277451 12527745 Abdominal pain upper
125277451 12527745 Anxiety
125277451 12527745 Arthralgia
125277451 12527745 Blood pressure increased
125277451 12527745 Disturbance in attention
125277451 12527745 Dizziness
125277451 12527745 Dyspnoea
125277451 12527745 Facial paralysis
125277451 12527745 Fatigue
125277451 12527745 Hypoaesthesia
125277451 12527745 Muscular weakness
125277451 12527745 Nausea
125277451 12527745 Panic attack
125277451 12527745 Presyncope
125277451 12527745 Tinnitus
125277451 12527745 Tremor
125277451 12527745 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
125277451 12527745 1 20140622 0
125277451 12527745 2 20160617 0
125277451 12527745 3 20120710 0