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
118336003 11833600 3 F 20160809 20151214 20160819 EXP US-TEVA-617517USA TEVA GOLOMB BA, KOSLIK HJ, REDD AJ. FLUOROQUINOLONE-INDUCED SERIOUS, PERSISTENT, MULTISYMPTOM ADVERSE EFFECTS. BMJ-CASE-REP 2015; :. 23.00 YR F Y 0.00000 20160819 MD US US

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
118336003 11833600 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Unknown 500MG 2 TIMES A DAY FOR 10 DAYS N 74124
118336003 11833600 2 SS MOXIFLOXACIN. MOXIFLOXACIN 1 Unknown 400MG DAILY FOR 3 DAYS N 77437

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118336003 11833600 1 Diarrhoea infectious
118336003 11833600 2 Oropharyngeal pain

Outcome of event

Event ID CASEID OUTC COD
118336003 11833600 DS
118336003 11833600 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118336003 11833600 Alopecia
118336003 11833600 Amnesia
118336003 11833600 Arthralgia
118336003 11833600 Cognitive disorder
118336003 11833600 Disturbance in attention
118336003 11833600 Dizziness
118336003 11833600 Dry eye
118336003 11833600 Dry mouth
118336003 11833600 Dyspnoea
118336003 11833600 Fatigue
118336003 11833600 Gastrointestinal pain
118336003 11833600 Gastrooesophageal reflux disease
118336003 11833600 Impaired gastric emptying
118336003 11833600 Insomnia
118336003 11833600 Irritable bowel syndrome
118336003 11833600 Micturition urgency
118336003 11833600 Migraine
118336003 11833600 Mood swings
118336003 11833600 Multiple chemical sensitivity
118336003 11833600 Muscle contractions involuntary
118336003 11833600 Muscular weakness
118336003 11833600 Myalgia
118336003 11833600 Mydriasis
118336003 11833600 Nausea
118336003 11833600 Orthostatic hypotension
118336003 11833600 Polyneuropathy
118336003 11833600 Postural orthostatic tachycardia syndrome
118336003 11833600 Seizure
118336003 11833600 Sinus disorder
118336003 11833600 Sinusitis
118336003 11833600 Tachycardia
118336003 11833600 Tendonitis
118336003 11833600 Toxicity to various agents
118336003 11833600 Ulcerative keratitis
118336003 11833600 Upper respiratory tract infection
118336003 11833600 Weight decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found